Drugs intended for human or veterinary use, presented in their finished dosage form. Included here are materials used in the preparation and/or formulation of the finished dosage form.
The analysis of a chemical substance by inserting a sample into a carrier stream of reagent using a sample injection valve that propels the sample downstream where mixing occurs in a coiled tube, then passes into a flow-through detector and a recorder or other data handling device.
Solid dosage forms, of varying weight, size, and shape, which may be molded or compressed, and which contain a medicinal substance in pure or diluted form. (Dorland, 28th ed)
Solution titration in which the end point is read from the electrode-potential variations with the concentrations of potential determining ions. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Homogeneous liquid preparations that contain one or more chemical substances dissolved, i.e., molecularly dispersed, in a suitable solvent or mixture of mutually miscible solvents. For reasons of their ingredients, method of preparation, or use, they do not fall into another group of products.
A phenothiazine with actions similar to CHLORPROMAZINE but with less antipsychotic activity. It is primarily used in short-term treatment of disturbed behavior and as an antiemetic.
Determination, by measurement or comparison with a standard, of the correct value of each scale reading on a meter or other measuring instrument; or determination of the settings of a control device that correspond to particular values of voltage, current, frequency or other output.
Completed forms of the pharmaceutical preparation in which prescribed doses of medication are included. They are designed to resist action by gastric fluids, prevent vomiting and nausea, reduce or alleviate the undesirable taste and smells associated with oral administration, achieve a high concentration of drug at target site, or produce a delayed or long-acting drug effect.
Drugs intended for DENTISTRY.
Electric conductors through which electric currents enter or leave a medium, whether it be an electrolytic solution, solid, molten mass, gas, or vacuum.
Determination of the spectra of ultraviolet absorption by specific molecules in gases or liquids, for example Cl2, SO2, NO2, CS2, ozone, mercury vapor, and various unsaturated compounds. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Macrocyclic polyethers with the repeating unit of (-CH2-CH2-O)n where n is greater than 2 and some oxygens may be replaced by nitrogen, sulfur or phosphorus. These compounds are useful for coordinating CATIONS. The nomenclature uses a prefix to indicate the size of the ring and a suffix for the number of heteroatoms.
A polyvinyl resin used extensively in the manufacture of plastics, including medical devices, tubing, and other packaging. It is also used as a rubber substitute.
Chemistry dealing with the composition and preparation of agents having PHARMACOLOGIC ACTIONS or diagnostic use.
Substances used for the detection, identification, analysis, etc. of chemical, biological, or pathologic processes or conditions. Indicators are substances that change in physical appearance, e.g., color, at or approaching the endpoint of a chemical titration, e.g., on the passage between acidity and alkalinity. Reagents are substances used for the detection or determination of another substance by chemical or microscopical means, especially analysis. Types of reagents are precipitants, solvents, oxidizers, reducers, fluxes, and colorimetric reagents. (From Grant & Hackh's Chemical Dictionary, 5th ed, p301, p499)
The presence of organisms, or any foreign material that makes a drug preparation impure.
An element of the rare earth family of metals. It has the atomic symbol Ce, atomic number 58, and atomic weight 140.12. Cerium is a malleable metal used in industrial applications.
Liquid chromatographic techniques which feature high inlet pressures, high sensitivity, and high speed.
An electrochemical technique for measuring the current that flows in solution as a function of an applied voltage. The observed polarographic wave, resulting from the electrochemical response, depends on the way voltage is applied (linear sweep or differential pulse) and the type of electrode used. Usually a mercury drop electrode is used.
Concentration or quantity that is derived from the smallest measure that can be detected with reasonable certainty for a given analytical procedure.
The application of scientific knowledge or technology to pharmacy and the pharmaceutical industry. It includes methods, techniques, and instrumentation in the manufacture, preparation, compounding, dispensing, packaging, and storing of drugs and other preparations used in diagnostic and determinative procedures, and in the treatment of patients.
The study of chemical changes resulting from electrical action and electrical activity resulting from chemical changes.
Substances made up of an aggregation of small particles, as that obtained by grinding or trituration of a solid drug. In pharmacy it is a form in which substances are administered. (From Dorland, 28th ed)
The art or process of comparing photometrically the relative intensities of the light in different parts of the spectrum.
The chemical and physical integrity of a pharmaceutical product.
The statistical reproducibility of measurements (often in a clinical context), including the testing of instrumentation or techniques to obtain reproducible results. The concept includes reproducibility of physiological measurements, which may be used to develop rules to assess probability or prognosis, or response to a stimulus; reproducibility of occurrence of a condition; and reproducibility of experimental results.
Hard or soft soluble containers used for the oral administration of medicine.
Methodologies used for the isolation, identification, detection, and quantitation of chemical substances.
A thiazide diuretic often considered the prototypical member of this class. It reduces the reabsorption of electrolytes from the renal tubules. This results in increased excretion of water and electrolytes, including sodium, potassium, chloride, and magnesium. It is used in the treatment of several disorders including edema, hypertension, diabetes insipidus, and hypoparathyroidism.
Artificially produced membranes, such as semipermeable membranes used in artificial kidney dialysis (RENAL DIALYSIS), monomolecular and bimolecular membranes used as models to simulate biological CELL MEMBRANES. These membranes are also used in the process of GUIDED TISSUE REGENERATION.
Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed)
A basis of value established for the measure of quantity, weight, extent or quality, e.g. weight standards, standard solutions, methods, techniques, and procedures used in diagnosis and therapy.
The normality of a solution with respect to HYDROGEN ions; H+. It is related to acidity measurements in most cases by pH = log 1/2[1/(H+)], where (H+) is the hydrogen ion concentration in gram equivalents per liter of solution. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
A nonmetallic element with atomic symbol C, atomic number 6, and atomic weight [12.0096; 12.0116]. It may occur as several different allotropes including DIAMOND; CHARCOAL; and GRAPHITE; and as SOOT from incompletely burned fuel.
Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.
Agents that are used to stimulate evacuation of the bowels.

The gas-liquid chromatograph and the electron capture detection in equine drug testing. (1/3191)

Three gas-liquid chromatographic (G.L.C.) procedures discussed have been designed around the four "esses" of detection tests--speed, sensitivity, simplicity, and specificity. These techniques are admirably applicable to the very low plasma drug levels encountered in blood testing under pre-race conditions. The methods are equally applicable to post-race testing procedures, where both blood and urine samples are tested. Drugs can only rarely be detected by the electron capture detector (E.C.D.) without a prior derivatization step, which conveys to the drug(s) high electron affinity. Because of broad applicability, two derivatizing agents, heptafluorobutyric (HFBA) and pentafluorpropionic (PFPA) anhydrides are employed. The three techniques, allowing broad coverage of various drug classes are: 1) direct derivatization of drugs to form strongly electron capturing amides and esters. 2) reductive fragmentation of drugs with lithium aluminum hydride to form alcohols, with conversion to ester derivatives. 3) oxidative fragmentation of drugs with potassium dichromate to form derivatizable groups, followed by direct derivatization.  (+info)

Report on use of XAD resins in racing chemistry. (2/3191)

This report comprises a summary of the work done with XAD resin extraction by racing chemists and reported in the Association of Official Racing Chemists publications. It is apparent that the use of XAD resins is becoming more popular in racing laboratories as a technique for routine screening and also for the extraction of certain conjugated drugs. Most laboratories employ variations on the original Brinkmann Drug-Skreen Technique. Comparisons of the efficiency of extraction of drugs from horse urine by XAD-2 resin and by chloroform column extraction indicate that some drugs can be extracted with equal or greater efficiency by the resin technique.  (+info)

Racing problems in the U.S.A. (3/3191)

The major problems of racing in the United States at the present time are caused by too much racing. This has led to too few horses and small fields. Consequently many owners and trainers are trying to enter their horses too frequently and to race them when they are not really fit to run. The desire to race horses as frequently as possible has led to constant pressure from horsemen through their organizations for so called "permissive medication". Started in the state of Colorado approximately ten years ago this has grown until finally there are only a few states, notably New York and New Jersey that have resisted the pressure. The drug that gave the opening wedge to permissive medication was phenylbutazone, but this in many states has led to the inclusion of other drugs including analgesics and drugs that veterinarians claim are needed for therapeutic purposes. Some states have endeavoured to control phenylbutazone medication by quantitation and while lower limits cause little difficulty, maximum allowable limits have caused problems and are not practical. While there has been no publicity to my knowledge about frusemide (furosemide, lasix) the abuse of this drug for so called "bleeders" is an example that may seriously interfere with drug detection in urine and its use should be confined to proven "bleeders" (i.e. horses suffering from epistaxis). Pre-race blood testing began roughly ten years ago at the harness tracks and has been resisted by our flat tracks rather successfully up to the present time. The blood testing methods and those used by the same laboratories in post-race urine testing is inadequate and will not detect many illegal drugs.  (+info)

Doping control in Japan. An automated extraction procedure for the doping test. (4/3191)

Horse racing in Japan consists of two systems, the National (10 racecourses) and the Regional public racing (32 racecourses) having about 2,500 racing meetings in total per year. Urine or saliva samples for dope testing are collected by the officials from thw winner, second and third, and transported to the laboratory in a frozen state. In 1975, 76, 117 samples were analyzed by this laboratory. The laboratory provides the following four methods of analysis, which are variously combined by request. (1) Method for detection of drugs extracted by chloroform from alkalinized sample. (2) Methods for detection of camphor and its derivatives. (3) Method for detection of barbiturates. (4) Method for detection of ethanol. These methods consist of screening, mainly by thin layer chromatography and confirmatory tests using ultra violet spectrophotometry, gas chromatography and mass spectrometry combined with gas chromatography. In the screening test of doping drugs, alkalinized samples are extracted with chloroform. In order to automate the extraction procedure, the authors contrived a new automatic extractor. They also devised a means of pH adjustment of horse urine by using buffer solution and an efficient mechanism of evaporation of organic solvent. Analytical data obtained by the automatic extractor are presented in this paper. In 1972, we started research work to automate the extraction procedure in method (1) above, and the Automatic Extractor has been in use in routine work since last July. One hundred and twnety samples per hour are extracted automatically by three automatic extractors. The analytical data using this apparatus is presented below.  (+info)

The antidoping control in horseraces in Italy. (5/3191)

The results and the improvement of the analytical procedures adopted for the control of doping in horses will be reported. This control has been systematically carried out in Italy for about 10 years in the laboratories of Italian Federation of Sport and Medicine in which the biological samples for the control of doping in various sport activities (football, cycling, athletics etc.) are also examined. In this way it is possible to use the same instruments for all these similar problems and compare the results. The analytical procedure is based on the following steps: 1) Extraction of the samples (mainly urine but sometimes blood or saliva). 2) Screening tests by thin-layer chromatography. 3) Confirmatory tests by gas chromatography on different columns and also by gas chromatography coupled with mass spectrometry. These single steps will be separately discussed, and practical problems encountered will be presented.  (+info)

Less common "doping" agents and substances encountered during routine screening for drugs. (6/3191)

The chromatographic and spectroscopic properties of several unusual substances which have been detected in the "alkaloidal" chloroform extract from racehorse urine and saliva samples are reported. Some of these substances have been identified by combined gas chromatography-mass spectrometry and the source of the substance is stated where this is known. Other substances whose identity is not known have been detected and their mass spectra show characteristic amine fragments. The occurrence of these unidentified substances is more frequent in aged urine samples and it would therefore appear that they are associated with putrefaction.  (+info)

Does the availability of prescribed drugs affect rates of self poisoning? (7/3191)

The trends in self-poisoning rates and in rates of prescribing of the major drug groups were compared. Over the period 1981-91, barbiturate prescribing and self poisoning both fell by 80%; for antidepressants, prescribing increased by over 40% and self poisoning by 30%; for antipsychotics, both rose by 30%; for benzodiazepines, poisoning fell by 30% and prescribing by 20%. Even for analgesic drugs, which are also available over the counter, there was a correspondence between changes in self poisoning and prescribing. The availability of prescribed drugs is directly related to their use for self poisoning. Restricting the availability of these drugs is a possible preventative strategy, although further research on this is needed.  (+info)

Drug-protein binding and blood-brain barrier permeability. (8/3191)

The permeability surface area (PS) product, an index of permeability of the blood-brain barrier (BBB), was measured by using the in situ perfusion method. In the cerebral circulation, the fraction of drug that permeates into the brain through the BBB is not only the unbound fraction but also the fraction dissociated from the protein in the perfusate. The sum of these two fractions, the apparent exchangeable fraction, was estimated by fitting the parameters of the BBB permeability under the condition of varying BSA concentrations in the perfusate. The unbound fraction of drugs in a buffer containing 0.5 mM BSA was measured by using the ultrafiltration method in vitro, and the apparent exchangeable fraction was measured in vivo by using the intracarotid artery injection method. The apparent exchange fraction was 100% for S-8510, 96.5% for diazepam, 90.9% for caffeine, 38.3% for S-312-d, 33.1% for propranolol, and 6.68% for (+)-S-145 Na, and each of these was higher than the corresponding unbound fraction in vitro in all drugs. The apparent exchangeable fractions, for example, were 8 times higher for diazepam and 38 times for S-312-d than the unbound fractions in vitro. The apparent exchangeable fraction of drugs was also estimated from the parameters obtained with the perfusion method. Because drugs can be infused for an arbitrary length of time in the perfusion method, substances with low permeability can be measured. The apparent exchangeable fractions obtained with this method were almost the same as those obtained with the intracarotid artery injection method.  (+info)

A comprehensive introduction for scientists engaged in new drug development, analysis, and approvals Each year the pharmaceutical industry worldwide recruits thousands of recent science graduates especially chemistry, analytical chemistry, pharmacy, and pharmaceutical majors into its ranks. However, because of their limited background in pharmaceutical analysis most of those new recruits find making the transition from academia to industry very difficult. Designed to assist both recent graduates, as well as experienced chemists or scientists with limited regulatory, compendial or pharmaceutical analysis background, make that transition, Pharmaceutical Analysis for Small Molecules is a concise, yet comprehensive introduction to the drug development process and analysis of chemically synthesized, small molecule drugs. It features contributions by distinguished experts in the field, including editor and author, Dr. Behnam Davani, an analytical chemist with decades of technical management and ...
Title:A UPLC-MS/MS Method for Simultaneous Determination of Six Bioactive Compounds in Rat Plasma, and its Application to Pharmacokinetic Studies of Naoshuantong Granule in Rats. VOLUME: 15 ISSUE: 3. Author(s):Ping Wang, Shenmeng Jiang, Yu Zhao, Shuo Sun, Xiaoli Wen, Xingjie Guo* and Zhen Jiang*. Affiliation:Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning Province, Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning Province, Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning Province, Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning Province, Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning Province, Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang ...
This study presents the evaluation of seven pharmaceutical compounds belonging to different commonly used therapeutic classes in seawater samples from coastal areas of Gran Canaria Island. The target compounds include atenolol (antihypertensive), acetaminophen (analgesic), norfloxacin and ciprofloxacin (antibiotics), carbamazepine (antiepileptic) and ketoprofen and diclofenac (anti-inflammatory). Solid phase extraction (SPE) was used for the extraction and preconcentration of the samples, and liquid chromatography tandem mass spectrometry (LC-MS/MS) was used for the determination of the compounds. Under optimal conditions, the recoveries obtained were in the range of 78.3% to 98.2%, and the relative standard deviations were less than 11.8%. The detection and quantification limits of the method were in the ranges of 0.1-2.8 and 0.3-9.3 ng·L−1, respectively. The developed method was applied to evaluate the presence of these pharmaceutical compounds in seawater from four outfalls in Gran Canaria Island
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ABSTRACT. The aim of this study is to present a Quick and Easy formula for the calculations of percent spike recovery of drug samples. Currently there are several cumbersome methods used in the determination of percent spike recovery in pharmaceutical analyses performed in various laboratories including the FDA laboratories around the world and especially in USA. In this paper we have compared the Quick & Easy Method using Pals formula against the method suggested by ORA Manual. The efficacy of this new formula has been demonstrated by seven examples including the main example of Pilocarpine hydrochloride discussed in detail. This Quick & Easy method is very simple, efficient and convenient way of determining percent spike recoveries and RPD values of duplicate spike solutions in drug analyses by HPLC, GC or UV methods. The simplicity of the method saves time and effort when compared to the existing method. Keywords: Pals formula, ORA Manual. ...
Current Pharmaceutical Analysis publishes authoritative reviews, written by experts in the field on all the most recent advances in pharmaceutical and biomedical analysis. All aspects of the field are represented including drug analysis, analytical methodology and instrumentation. The journal is essential to all involved in pharmaceutical, biochemical and clinical analysis.. ...
Pharmaceutical Drugs are defined as chemical substances used for treating, curing and preventing different types of diseases. Commonly referred as medicines or medication, pharmaceutical drugs are used in the medical diagnosis, treatment, prevention or curing disease. For varied diseases, physical ailments, there are a wide range of pharmaceutical drugs which are available over the counter (OTC) or with doctors advise.
Our GMP pharmaceutical laboratories provide chemistry, manufacturing and controls (CMC) analytical laboratory services in accordance with current Good Manufacturing Practice (cGMP). Intertek provides cGMP compliant pharmaceutical analysis services that meet the requirements of regulatory authorities worldwide. Laboratory services supporting GMP and CMC requirements range from early development characterization, formulation support analysis, stability testing and method development and method validation through to GMP batch release testing. Our experienced scientists can support your development or manufacturing activities for both small molecule pharmaceuticals and biopharmaceuticals such as proteins, monoclonal antibodies and vaccines. Our GMP laboratory teams have extensive experience with drug delivery systems, drug device combinations and a wide range of medical devices.. cGMP Compliant Analytical Laboratories:. ...
Capillary Electrophoresis (CE) | Separation Science Pharmaceutical Analysis (www.pharma-sci.com) offers free learning from the experts covering methods, applications, webinars, videos, tutorials for pharmaceutical and biopharmaceutical analysis users of chromatography, mass spectrometry, sample preparation and related analytical techniques.
Useni Reddy Mallu is an editor of Edelweiss Pharma Analytic Acta journal, whose research interests currently includes Pharmaceutical Analysis, Pharmaceutical Regulatory affairs and Drug delivery system.
Pharmaceutical Analysis, 978-3-659-63956-2, This research focuses on the in vitro evaluation of commercially available marketed antacid preparation (tablet) in Bangladesh. This research work deals with chewable non - systemic antacid preparations which are usually used in combination. We have done our experimental work by measuring the acid - neutralizing capacity in two ways. These are simple complexometric titration method and pH measurement method. Then we compare those results. Then we have done assay of those antacid preparations. And we also work various tests for evaluation of tablet. These are weight variation test, thickness and diameter, hardness test. Ultimately our goal is to know about those antacid preparation (tablet) are maintain BP specification and they are how much acceptable.
This title simplifies the understanding of the basic principles of Pharmaceutical Analysis by bridging the gap between the basics and complex topics such as spectrometry, chromatography, and various thermal analysis techniques. The title is a must-read for pharmacy graduates.
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Molecular Spectroscopy Market by Technology (NMR (FT - UV-VIS spectroscopy is routinely These bonds absorb the energy in the form of ultraviolet or visible light to Course in Pharmaceutical Analysis
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polysaccharide (9.522) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [triterpene (5.647) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [ganoderic acid (5.384) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [lucidenic acid (2.999) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [Gl-PS (2.998) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [lanostanoid (2.645) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [ergosterol (2.234) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [laccase (2.230) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [proteoglycan (1.997) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [F3 (1.993) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [terpenoid (1.987) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [more] [Help ...
Capillary Electrophoresis (CE) was explored as a means for physicochemical and biopharmaceutical characterisation of small drug molecules. Special attention was paid to the characterisation of acid-base and lipophilic properties of drug compounds by analysing their migration behaviour in different CE systems. The thesis comprises an overview of the field together with separate studies on the different topics.. The utility of CE for the determination of pKa of labile drug compounds was investigated. A general methodology was developed comprising key steps such as the use of a stabilising sample diluent, electromigration injection, and analyte characterisation by UV-Vis spectroscopy. The methodology was successfully applied for two sets of drug compounds, labile at low and high pH, respectively.. CE was also evaluated for experimental modelling of passive intestinal membrane permeability by studying analyte migration in liposomal, microemulsion and micellar electrolytes. Good correlation is ...
An analytical method for the simultaneous determination of eight pharmaceutical compounds in biosolids from urban wastewater treatment plants (WWTPs) was developed and validated. The compounds evaluated were non-steroidal anti-inflammatory drugs (naproxen, diclofenac, and ibuprofen), lipid regulators (clofibric acid), and antibiotics (sulfathiazole, sulfapyridine, sulfamethazine, and sulfamethoxazole). Ultrasound assisted extraction with a water-methanol solvent mixture (1:1, v:v) was performed and the compounds were then determined by liquid chromatography coupled with tandem mass spectrometry. The design of the method was based on the application of the standard addition calibration methodology to reduce matrix interferences. Validation procedures were conducted with rabbit excrements as blank samples. Recoveries of the target analytes ranged from 76 to 131% in spiked samples at 50, 200 or 1000 ng g−1 dry weight (dw). The relative standard deviations were in the range of 5-15% and the method ...
HPLC Application #15626: Pharmaceutical Compounds by Luna 3µ C18(2) MercuryMS Cartridge 20 x 4.0mm. Column used: Luna® 3 µm C18(2) 100 Å, LC Column 20 x 4 mm, Mercury, Ea Part#: 00M-4251-D0-CE
TY - JOUR. T1 - High-throughput screening for drugs of abuse and pharmaceutical drugs in hair by liquid-chromatography-high resolution mass spectrometry (LC-HRMS). AU - Pascali, Vincenzo Lorenzo. AU - Strano Rossi, Sabina. AU - Odoardi, Sara. AU - Valentini, Valeria. AU - De Giovanni, Nadia. PY - 2017. Y1 - 2017. N2 - A liquid chromatography-high resolution mass spectrometry (LC-HRMS) method for the simultaneous screening in hair samples of drugs of abuse and medicaments was developed. Target analytes screened using a single extraction and analytical run were opiates, cocaine, amphetamines and amphetamine-like substances, ketamine and analogues, cannabinoids, both natural and synthetic, cathinones, piperazines, ephedrines and others new psychoactive substances not pertaining to these classes; pharmaceutical drugs such as antipsychotics, antiepileptics, antidepressants, benzodiazepines and analogues, anorectics, stimulants, drugs for the erectile dysfunction. The multiresidual method involved ...
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HEALTHY LIFE PHARMA PVT. LTD., a WHO GMP Certified Company, Manufacturer, Supplier, Exporter of Generic Pharmaceutical Drugs based in Mumbai, Maharashtra, India & offering best quality Generic Pharmaceutical Drugs to our clients.
China Pharmaceutical Drug Glimepiride 93479-97-1 for Treating Diabetes, Find details about China Glimepiride, 93479-97-1 from Pharmaceutical Drug Glimepiride 93479-97-1 for Treating Diabetes - Wuhan Lianshangwang Technology Co., Ltd.
A method is disclosed for delivering molecules such as pharmaceutical drugs and nucleic acids into skeletal muscle in vivo. The pharmaceutical drug or nucleic acid is first injected into the muscle at
TY - JOUR. T1 - Drug compound characterization by mass spectrometry imaging in cancer tissue. AU - Kwon, Ho Jeong. AU - Kim, Yonghyo. AU - Sugihara, Yutaka. AU - Baldetorp, Bo. AU - Welinder, Charlotte. AU - Watanabe, Ken Ichi. AU - Nishimura, Toshihide. AU - Malm, Johan. AU - Török, Szilvia. AU - Döme, Balázs. AU - Végvári, Ákos. AU - Gustavsson, Lena. AU - Fehniger, Thomas E.. AU - Marko-Varga, György. PY - 2015/9/22. Y1 - 2015/9/22. N2 - MALDI mass spectrometry imaging (MSI) provides a technology platform that allows the accurate visualization of unlabeled small molecules within the two-dimensional spaces of tissue samples. MSI has proven to be a powerful tool-box concept in the development of new drugs. MSI allows unlabeled drug compounds and drug metabolites to be detected and identified and quantified according to their mass-to-charge ratios (m/z) at high resolution in complex tissue environments. Such drug characterization in situ, by both spatial and temporal behaviors within ...
Expertise:. » Isolation, characterization and evaluation of bioactive constituents from herbal extracts using bioactivity guided fractionation. » Computer aided Drug Design (in silico analysis), synthesis and pharmacological evaluation (in vitro analysis) » Resolution of drugs, including enzymatic resolution and its monitoring. » Chiral chromatography » Forced degradation studies, Impurity profiling and development of stability indicating assays. » Analytical method development and validation » Synthesis, purification and characterization of impurities/metabolites. » Structural Elucidation using spectroscopic techniques » Bioanalytical method development and validation; Therapeutic Drug Monitoring » Drug metabolism and pharmacokinetic analysis » Herbal Analysis » In vitro analysis for antibacterial, antifungal and antiamoebic activity Go to TOP ...
A rapid and simple method of spectrophotometric estimation Empagliflozin in UV-region was developed and validated according to International Conference on Harmonization (ICH Q2 R1) guidelines. The standard and sample solutions were prepared using ethanol and water. The maximum absorbance (?max) was obtained at 223 nm. The calibration curve was linear in the range of 1-30µg/ml. The %RSD for intra and inter-day precision was found to be 0.29 and 0.39 respectively. Recovery studies of Empagliflozin were within 99.20% to 99.49 and assay was found to be 99.87% and LOD and LOQ was found to be 0.10 and 0.33 respectively. The %RSD for robustness was found to be between 0.20 and %RSD for ruggedness was found to be 0.03. The proposed method was found to be rapid, precise, accurate and can be adaptable for routine analysis of Empagliflozin bulk and marketed dosage forms.
In the Laboratory of Drug Quality and Registration (DruQuaR) fundamental and applied research is carried out in the fields of pharmaceutical analytics and regulatory affairs.. Our general research goal is studying the functional quality of pharmaceuticals and related products. Emphasis is placed on the following, more specific topics:. ...
In the present study, a new, simple and cheap shaker-assisted deep eutectic solvent microextraction (SA-DESME) procedure was developed for extraction of paracetamol in synthetic urea and pharmaceutical samples prior to its determination by UV-VIS spectrophotometer. The SA-DES-ME procedure is based on the selective extraction of paracetamol which deep eutectic solvents (DESs) prepared with choline chloride (ChCI)/betaine (Bet) and different hydrogen bond donors (HBDs).The DESs was used as the extraction solvent for the separation of the paracetamol-containing complex from the sample solution. Optimum values of experimental parameters were determined by univariate optimization method. Under optimum conditions, analytical results such as good linearity (50-800 mu g L-1), quantitative recoveries (94.2-107.1%), low detection limit (14.9 mu g L-1), and high sensitivity enhancement factor (135) were obtained using the proposed method. Additionally, the relative standard deviations (RSDs%) were less ...
508834031 - EP 3345600 A4 20190410 - MIRABEGRON-CONTAINING TABLET, METHOD FOR PRODUCING MIRABEGRON-CONTAINING PHARMACEUTICAL PREPARATION AND METHOD FOR PRODUCING MIRABEGRON-CONTAINING GRANULATED PRODUCT - [origin: EP3345600A1] [Problem] To provide a mirabegron-containing tablet which retains the amorphous state of mirabegron after long-term storage; a mirabegron-containing pharmaceutical preparation capable of retaining mirabegron purity by preventing analog formation during storage; a method for producing a mirabegron-containing pharmaceutical preparation; and a method for producing a mirabegron-containing granulated product. [Solution] According to one embodiment of the present invention, provided is a mirabegron-containing pharmaceutical preparation, characterized in comprising mirabegron, and hypromellose and polyvinyl pyrrolidone. The mirabegron-containing pharmaceutical preparation may comprise a spray-dried granulated product comprising the mirabegron and the hypromellose and the polyvinyl
This moment version of a world bestseller has been thoroughly redesigned and broadly rewritten take into consideration the recent caliber via layout (QbD) and lifecycle ideas in pharmaceutical manufacturing.. As within the first variation, the elemental specifications for analytical technique validation are lined, however the moment variation describes how those are utilized systematically in the course of the whole analytical lifecycle. QbD ideas require adoption of a scientific method of improvement and validation that commence with predefined ambitions. For analytical equipment those predefined goals are verified as an Analytical goal Profile (ATP). The booklet chapters are aligned with lately brought criteria and instructions for production methods validation and stick with the 3 levels of the analytical lifecycle: technique layout, strategy functionality Qualification, and persisted technique functionality Verification. Case stories and examples from the pharmaceutical illustrate the ...
A simple, accurate, precise, sensitive and a highly selective ultra violet spectrophotometric method has been developed for the simultaneous estimation of in bulk and solid dosage form. The estimation of Zidovudine was carried out at 266 nm. The developed method was validated for linearity, range, precision, recovery studies and interference study for mixture. All these parameters showed the adaptability of the method for the quality control analysis of the drug in bulk and in marketed formulations.
Micellar liquid chromatography (MLC) is an analytical technique belonging to the wide range of reversed-phase liquid chromatographic (RP-LC) separation techniques. MLC with the use of surfactant solutions above its critical micellar concentration (CMC) and the addition of organic modifiers is currently an important analytical tool with still growing theoretical considerations and practical applications in pharmaceutical analysis of drugs and other biologically active compounds. The use of MLC as an alternative, relatively much faster in comparison to conventional chromatographic separation techniques has several advantages, especially as being suitable for screening pharmaceutical analysis. The analytical data received from MLC analysis are considered a useful source of information to predict passive drug absorption, drug transport and other pharmacokinetics and physicochemical measures of pharmaceutical substances. In the review several MLC assays for determination of drugs and other active ...
Crystallinity and Why It Is Important for Pharmaceuticals. The term crystalline is used to describe solids in which the atoms or molecules are arranged in an ordered manner. For many pharmaceuticals, the crystalline form is more kinetically stable than the amorphous form, which typically results in crystalline solids being less soluble, and therefore less bioavailable than their amorphous counterparts. The influence that crystallinity has over the solubility of a solid is what makes this an important factor when manufacturing pharmaceuticals, as those which are supposed to be fast-acting should be readily soluble in the body, while slow-acting drugs should dissolve relatively slowly. This has been shown to be the case in previous studies of bioavailability of APIs in the literature (3-5). Because of this, it is important to be able to control the crystallinity of a drug and monitor it. However, the crystallinity of a sample cannot be assumed to be simply either 100% ordered or 100% amorphous. ...
Ottergemsesteenweg 460, 9000 Ghent (Belgium). Phone: + 32 (0)9 264.81.01. E-mail: [email protected] PhD Research:. Title: Somatropin derivatives for imaging and treatment of GH-R expressing melanoma. Summary:. Melanoma is considered to be one of the deadliest cancers worldwide. Originating from melanocytes in skin and mucosa with metastasis to other organs, it is difficult to treat. Human growth hormone (hGH) and the growth hormone-receptor (GHR) are normally involved in regulatory processes like metabolism, balanced growth, and cell differentiation. However, the human GHR was found to be over-expressed in i.a. different melanoma cell lines and may thus play a role in metastasis and invasion of human melanoma. Derivates of somatropin (i.e. recombinantly produced hGH) show potential to visualize and treat these types of cancer in humans.. The main goal of this research is to develop a tumor-selective protein drug for use in diagnosis and treatment of melanoma. Somatropin and its ...
Dr Khaled H Assi obtained his BSc in the Sciences of Chemistry in 1994 and was awarded the PhD in pharmaceutical analysis by the University of Bradford, in 1999.. He then took up a post doctoral post at university of Bradford between 1999-2001 working on the inhaled therapies. His post doctoral program was extended for one more year through an awarded grant from Glaxo SmithKline joint with Professor H Chrystyn .. In 2002, he was accepted a research fellowship at Bradford School of Pharmacy. Dr Assi was appointed as a Lecturer at the Bradford School of Pharmacy, in July 2004 and has continued developing his research in the inhaled therapies area. In this position he is teaching the pharmacy and pharmaceutical management students at different levels. The modules he delivers cover the area of pharmaceutical analysis, Quality assurance and quality control of pharmaceuticals.. He is also active in the research. His research interests cover the inhalation therapies and developing of pharmaceutical and ...
|p|Get an introduction to pharmaceuticals from drug discovery to manufacture, and learn to use the  tools needed for their analysis.|/p|
This 2-day HPLC course is aimed at those who are new to the technique of HPLC and want to use it for the analysis of pharmaceuticals. The training course is delivered at your companys site by the MTS trainer. A pre-training visit may be arranged during which the MTS trainer will discuss the content of the training course with you to ensure that the HPLC training is fully tailored to your needs.
Purchase the latest market research you need on the Pharmaceutical Industry in India. Click here to find the reports from reputable publishers.
Paper analytical devices (PADs) are test cards that can quickly determine whether a drug tablet contains the correct medicines. They are cheap and easy to use. They dont require power, chemicals, solvents, or any expensive instruments, so they can be deployed rapidly at large scale whereever a problem with pharmaceutical quality is suspected.
MILAN, December 4, 2012 /PRNewswire/ --. Last month, 55 of Europes biggest players from across the pharmaceutical drug discovery sector convened for two-and-a-half days as they attended the most disruptive event of the year - GDS Internationals fourth Next Generation Pharmaceutical Drug Discovery summit (NGP DD EU), held at the Meliá Milano Hotel, Milan, Italy.. Europe has been an enduring force in the pharmaceutical industry for decades. However, increased competition due in part to globalisation, economic recession and ICT advancements has levelled the playing field for drug discovery. Wise investment and innovative new technologies are subsequently proving key to staying ahead of competitors. With this in mind, GDS International has created an award to recognise exceptional talent within the sector.. Selected as the winners by a panel of 20 senior executives from the R&D functions of global biopharma companies, Paul ORiordan - CEO of Synexa Life Sciences, and Henning Steinhagen - SVP Head ...
McCarthy , Kelly LLP lawyers have represented individuals that have been injured by a variety of pharmaceutical drugs. Our lawyers have many years of experience litigating cases against manufacturers of defective product including members of the pharmaceutical industry. McCarthy , Kelly LLP lawyers and staff represent individuals who were injured through the use of pharmaceutical drugs and provide our clients with up-to-date information about the drug and their legal options.. ...
In the past, people used herbs as a form of treatment for illness. Nowadays, the mainstream belief is that they are not as effective and not worth taking. For each health issue people use pharmaceutical drugs. This is because effectiveness of each herb and their use has not been studied deeply to determine how effective it can be. On the other hand, pharmaceutical drugs are attempted to mimic a compound that occurs naturally in nature (herbs). They can also bring the risk of side effects.. According to stats released by the American Association of Poison Control Centers, no deaths have been reported due to the use and consumption of herbs. However, pharmaceutical drugs and physician prescribed medications kill approximately one million Americans each year. It is important to note that herbal medicines can be lethal in extreme doses it appears their safety is much greater than that of pharmaceutical drugs.. Pharmaceutical drugs can have side effects on human health. For example antibiotics in ...
LI Song;NI Hai-tao;SHENG Xia;TANG Shou-yan;LU Wen-jing;CHENG Chun-yan;LI Wei;FAN Guo-rong;SUN Ying-hao;GCP Office,Department of Urology,Changhai Hospital,Second Military Medical University;Department of Pharmaceutical Analysis,School of Pharmacy,Second Military Medical University & Key Laboratory of Shanghai Drug(Chinese Materia Medica)Metabolism Research;Department of Pharmaceutical Analysis,School of Pharmacy,Shenyang Pharmaceutical University;Department of Histology and Embryology,College of Basic Medical Sciences,Second Military Medical University; ...
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MEDIPHAR LIFESCIENCES PRIVATE LIMITED - We have managed to make our company the trusted name in the industry as supplier and distributor of highly effective Allopathic Medicine, Pharmaceutical Medicine, Pharmaceutical Drugs, Pharmaceutical Injection for several health issues.Located in Chandigarh,India.
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McKesson Corporation (McKesson), one of the nations largest distributors of pharmaceutical drugs, agreed to pay a record $150 million civil penalty for alleged violations of the Controlled Substances Act (CSA), the Justice Department announced today. The nationwide settlement requires McKesson to suspend sales of controlled substances from distribution centers in Colorado, Ohio, Michigan and Florida for multiple years. The staged suspensions are among the most severe sanctions ever agreed to by a Drug Enforcement Administration (DEA) registered distributor. The settlement also imposes new and enhanced compliance obligations on McKessons distribution system. In 2008, McKesson agreed to a $13.25 million civil penalty and administrative agreement for similar violations. In this case, the government alleged again that McKesson failed to design and implement an effective system to detect and report suspicious orders for controlled substances distributed to its independent and small chain pharmacy ...
These people all knew why talking therapies are better than pharmaceutical drugs in the treatment of depression. They have described so much more succinctly the power of the mind over our mental health than ever I could ...
Wholesale Trader of Pharmaceutical Drugs - Dexmethasone Injection 5ml, Dexmethasone Injection 10ml offered by Vinson Pharma (A Div. Of Vintek Pharmaceutials), Chandigarh.
Rodent Research-6 (RR-6) is a two-fold investigation that will study the effectiveness of both the drug compound and the nano-channel drug delivery implant HOUSTON, TX, January 27, 2018 /24-7PressRelease/ - Extended spaceflight takes a toll on many systems within the human body, including the musculoskeletal system. An investigation aboard the International Space Station will examine a drug compound and drug delivery system aimed at preventing, slowing, or even reversing muscular breakdown, both in space and on Earth.. Rodent Research-6 (RR-6) is a two-fold investigation that will study the effectiveness of both the drug compound and the nano-channel drug delivery implant, for their use in the treatment of muscle loss in future spaceflight, and in the treatment of patients with muscle wasting diseases or conditions on Earth.. The drug compound will be administered through a device implanted beneath the skin, allowing for a constant, steady delivery of the drug.. The unique aspect of the mission ...
0187]Pharmaceutical agent as used herein refers to any of a variety of drugs or pharmaceutical compounds that can be used as active agents to prevent or treat a disease (meaning any treatment of a disease in a mammal, including preventing the disease, i.e. causing the clinical symptoms of the disease not to develop; inhibiting the disease, i.e. arresting the development of clinical symptoms; and/or relieving the disease, i.e. causing the regression of clinical symptoms). It is possible that the pharmaceutical agents of the invention may also comprise two or more drugs or pharmaceutical compounds. Pharmaceutical agents, include but are not limited to antirestenotic agents, antidiabetics, analgesics, antiinflammatory agents, antirheumatics, antihypotensive agents, antihypertensive agents, psychoactive drugs, tranquilizers, antiemetics, muscle relaxants, glucocorticoids, agents for treating ulcerative colitis or Crohns disease, antiallergics, antibiotics, antiepileptics, anticoagulants, ...
TABLE-US-00016 TABLE 3 LEVOSALBUTAMOL S04 - Form III Peak No. 2θ (deg) d (A) Height Height % FWHM 1 5.496 16.0657 2337 41.8 0.206 2 6.901 12.799 320 5.7 0.295 3 7.340 12.034 1938 34.6 0.217 4 8.181 10.7983 2348 42.0 0.645 5 8.399 10.5187 5559 99.4 0.251 6 10.978 8.0527 577 10.3 0.190 7 11.758 7.5203 978 17.5 0.178 8 12.778 6.9221 365 6.5 0.186 9 14.298 6.1895 565 10.1 0.233 10 14.701 6.0206 428 7.7 0.165 11 16.321 5.4266 4839 86.5 0.292 12 16.981 5.2172 498 8.9 0.134 13 17.980 4.9293 1110 19.8 0.319 14 18.180 4.8758 1421 25.4 0.532 15 18.660 4.7512 4455 79.6 0.432 16 18.860 4.7013 3247 58.0 0.243 17 19.189 4.6215 636 11.4 0.100 18 20.179 4.3969 797 14.2 0.529 19 20.720 4.2833 2355 42.1 0.315 20 22.019 4.0335 5594 100.0 0.306 21 22.219 3.9976 2598 46.4 0.595 22 23.121 3.8436 761 13.6 0.563 23 23.640 3.7604 2729 48.8 0.460 24 23.858 3.7265 2189 39.1 0.547 25 24.638 3.6103 654 11.7 0.168 26 25.339 3.5120 1235 22.1 0.276 27 25.721 3.4607 445 8.0 0.215 28 26.299 3.3859 414 7.4 0.352 29 26.518 3.3585 ...
According to the Gate-Control Theory of pain: a)we cannot control the gate through which pain enters or is emitted back from the brain b)the gate for pain is open only for survival instincts c)pain cannot pass through these special ...
The production of salt or cocrystalline forms is a common approach to alter the physicochemical properties of pharmaceutical compounds. The goal of this work was to evaluate the impact of anion choice (succinate, adipate, and sulfate) on the physicochemical characteristics of salbutamol forms. Novel crystals of salbutamol were produced by solvent evaporation: a cocrystal of salbutamol hemiadipate with adipic acid (salbutamol adipate, SA), salbutamol hemisuccinate tetramethanolate (SSU.MeOH), and its desolvated form (SSU). The crystalline materials obtained were characterized using thermal, X-ray, nuclear magnetic resonance, Fourier transform infrared spectroscopy, dynamic vapor sorption (DVS), and elemental analysis. The crystal forms of SA and SSU.MeOH were determined to be triclinic, (P?i), and monoclinic, (P21/n), respectively. DVS analysis confirmed that SSU and SA do not undergo hydration under increased relative humidity. Both thermal and elemental analyses confirmed the stoichiometry of ...
Introduction: Drug checking as a part of drug harm-reduction strategies represents an essential aspect of public health policies. It focuses on rapid identification of drugs that individuals intend to use during night events, in order to implement health-protective behaviors. Chemical drug analysis techniques vary considerably, from simple colorimetric reagents to advanced forensic methods such as gas chromatography/mass spectrometry (GC/MS).Materials and Methods: In 2019, drug-check services were offered at some night events in Umbria (Central Italy). One hundred and twenty attendees directly delivered unidentified substances to a harm-reduction worker, who collected a few milligrams of the substances on ceramic plates and added a drop of colorimetric reagent. Multiple reagents were used to increase the diagnostic capacity of a substance, which may react with a specific drug or a few drugs. Later, a fraction of the samples was analyzed by GC/MS. The concordance of the results obtained using these two
SRS pharma, India is a Pharmaceutical Manufacturer & Exporter of quality drugs. SRS Pharmaceutical Manufactures drugs like ACE Inhibitors,Hypertensives, Calcium Channel Blockers etc.
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Arlington, TX (PRWEB) September 07, 2016 -- Registration is now open for Serious Science: Advanced Course in Blood Drug Analysis and Trial Advocacy, an
The goal of this PhD work is to evaluate the possibilities of supercritical fluid chromatography (SFC) in the pharmaceutical analysis. This chromatographic approach will be used to develop analytical methods for numerous types of drugs (including chiral ones) in pharmaceutical formulations. Some inventive strategies will be developed to maximize performance and apply SFC to the widest possible range of molecules. The performance of SFC will be systematically compared to liquid chromatography (LC). In parallel, the PhD candidate will also have the opportunity to couple SFC with single quadrupole(MS), triple quadrupole (MS/MS) and high resolution (QqTOF/MS) mass spectrometers available in our laboratory. This instrumental setup will be used for the determination of drugs and metabolites in complex matrixes, such as biological fluids.. ...
Start Over You searched for: Languages Spanish ✖Remove constraint Languages: Spanish Languages French ✖Remove constraint Languages: French Languages Italian ✖Remove constraint Languages: Italian Copyright Public domain ✖Remove constraint Copyright: Public domain Subjects Pharmaceutical Preparations -- administration & dosage ✖Remove constraint Subjects: Pharmaceutical Preparations -- administration & dosage Titles How to get the best results from using Dr. Miles Nervine Liquid ✖Remove constraint Titles: How to get the best results from using Dr. Miles Nervine Liquid Dates by Range 1900-1949 ✖Remove constraint Dates by Range: 1900-1949 ...
Start Over You searched for: Authors Dr. Miles Medical Co., author. ✖Remove constraint Authors: Dr. Miles Medical Co., author. Languages German ✖Remove constraint Languages: German Copyright Public domain ✖Remove constraint Copyright: Public domain Subjects Pharmaceutical Preparations -- administration & dosage ✖Remove constraint Subjects: Pharmaceutical Preparations -- administration & dosage Titles How to get the best results from using Dr. Miles Nervine Liquid ✖Remove constraint Titles: How to get the best results from using Dr. Miles Nervine Liquid ...
The 2016-2021 World Outlook for Pharmaceutical Preparations Affecting the Central Nervous System and Sense Organs The 2016-2021 World Outlook for Pharmaceutical Preparations Affecting the Central - Market research report and industry analysis - 9157883
Author: Allen Loyd V Jr, Year: 2019, Abstract: Process analytical technology was introduced by the U. S. Food and Drug Administration about 20 years ago to assist the pharmaceutical industry in making changes that should reduce batch failures, ensure performance, and enhance quality. Its premise is that
Professor David Woolfson holds the Chair in Pharmaceutics (Drug Delivery). He is a graduate in Pharmacy from Queens and is a registered pharmacist. Prof. Woolfson founded the McClay Research Centre for Pharmaceutical Sciences, from initial concept through to raising of the necessary funding. Starting as a lecturer in pharmaceutical analysis, he was appointed Reader in Pharmaceutical Sciences in 1991 and to the Chair in Pharmaceutics in 1995. He is Head of the School of Pharmacy at Queens.. Prof. Woolfson became a member of the British Pharmacopoeia Commission (BPC) in 1997 and was appointed as Chair of the BPC in 2006. The Commission is responsible under the UK Medicines Act for the annual publication of the British Pharmacopoeia., which sets legally enforceable quality standards for medicinal chemicals, drugs and formulated products. He has extensive experience of work in the European Pharmacopoeia Commission (EPC) as leader of the UK delegation and formerly UK Expert on Formulated Medicinal ...
PI & PI Biotech Inc. is mainly engaged in the custom synthesis, separation and purification of drug Impurities, highly pure natural compounds and APIs & intermediates, and pharmaceutical analysis.
2015 was a good year for innovation in medicine in both the EU and the US, according to data published on Monday (4 January).. The European Medicines Agency (EMA) recommended 93 new products, including generics, up from 82 in 2014. Across the Atlantic, the Food and Drug Administration (FDA) approved 45 novel drugs, four more than in 2014 and the most since the all-time record of 53 set in 1996.. But despite the rosy statistics and the prospect for further progress in 2016, the pharmaceuticals industry faces challenges, with increased political focus on drug pricing having punctured both biotech and specialty pharma valuations in recent months.. The prospect of Hillary Clinton becoming president of the United States could further undermine confidence in the sectors profitability in 2016, given her pledge to rein in drug costs. But any changes in the US pricing model are likely to be gradual, according to Bernstein analyst Tim Anderson.. Big pharmaceutical companies, meanwhile, are still ...
Del Mar Photonics offer a handheld infrared spectrometer based on the acousto-optic tunable filter (AOTF). This instrument is about the size and weight of a video camera, and can be battery operated. This unique, patented device is all solid-state with no moving parts. It has been sold for a wide variety of applications such as liquid fuel analysis, pharmaceutical analysis, gas monitoring and plastic analysis. Miniature AOTF infrared spectrometer uses a crystal of tellurium dioxide to scan the wavelength. Light from a light source enters the crystal, and is diffracted into specific wavelengths. These wavelengths are determined by the frequency of the electrical input to the crystal. Since there are no moving parts, the wavelength scanning can be extremely fast. In addition, specific wavelengths can be chosen by software according to the required algorithm, and therefore can be modified without changing the hardware. After the infrared radiation reflects off of the sample, it is converted into an ...
Del Mar Photonics offer a handheld infrared spectrometer based on the acousto-optic tunable filter (AOTF). This instrument is about the size and weight of a video camera, and can be battery operated. This unique, patented device is all solid-state with no moving parts. It has been sold for a wide variety of applications such as liquid fuel analysis, pharmaceutical analysis, gas monitoring and plastic analysis. Miniature AOTF infrared spectrometer uses a crystal of tellurium dioxide to scan the wavelength. Light from a light source enters the crystal, and is diffracted into specific wavelengths. These wavelengths are determined by the frequency of the electrical input to the crystal. Since there are no moving parts, the wavelength scanning can be extremely fast. In addition, specific wavelengths can be chosen by software according to the required algorithm, and therefore can be modified without changing the hardware. After the infrared radiation reflects off of the sample, it is converted into an ...
Received:10-07-2016 Revised: 12-08-2016 Accepted:18-08-2016 *Corresponding author: Shakeena G, Department of Pharmaceutical Analysis and Quality Assurance, Green Royal..
Researchers at Yangzhou University in China have employed fluorophotometry - a process used for quality control and pharmaceutical analysis - to deter
IMGT?, the worldwide ImMunoGeneTics information program? (http://www. and useful data released within the immunogenetics field keeps growing and involves fundamental exponentially, scientific, veterinary, and pharmaceutical analysis. The accurate amount of potential proteins types of the antigen receptors, immunoglobulins (IG) and T cell receptors (TR) is nearly unlimited. The repertoire of every individual is normally approximated to comprise about 1012 different IG (or antibodies) and TR, as well as the restricting factor is the amount of B and T cells an organism is normally genetically programmed to create. This huge variety is normally natural to the especially complex and exclusive molecular synthesis and genetics from the antigen receptor stores. This includes natural mechanisms such as for example DNA molecular rearrangements in multiple loci (three for IG and four for TR in human beings) situated on different chromosomes (four in human beings), nucleotide deletions and insertions on the ...
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The analysis of large intact proteins and complex biological samples containing drug molecules is a common complicated task for many scientists. However, due to the importance of these molecules, there is a growing interest in pharmaceutical and medicinal research to develop rapid, highly sensitive and efficient analytical techniques. The advantages of capillary electrophoresis (CE) in combination with mass spectrometry (MS) provide a powerful analytical tool. However, further improvement and development of these techniques are required to extend their utility and to meet the challenges of selected analytes. Thus, the scope of this thesis deals with the development of novel analytical methods to achieve efficient and high performance analysis of peptides, intact proteins, digests of complex samples and basic pharmaceutical drug compounds in biological matrices.. Implementation of CE for routine analysis of proteins and complex samples is constrained by the partial adsorption to the capillary ...
Ketoconazole containing medications, Ketoconazole indications and usages ATC and ICD codes, combinations with other active ingredients and trade names information from Drugs-about.com
Ferrous Sulfate containing medications, Ferrous Sulfate indications and usages ATC and ICD codes, combinations with other active ingredients and trade names information from Drugs-about.com
Food coloring Colorings are added to food to replace colors lost during preparation, or to make food look more attractive. ... Also used as a flavoring agent in pharmaceutical and food industries. Corn oil - one of the most common, and inexpensive ... mouthwashes and pharmaceuticals, as well as in aromatherapy and other medicinal applications. Metatartaric acid - food acid, ...
In 2017, in preparation for the 2020 Summer Olympic and Paralympic Games hosted in Tokyo, the Health, Labor and Welfare ... Court affirmed the Circuit Court's ruling that the Food and Drug Administration could not class tobacco as a pharmaceutical, so ... In the late nineteenth century, following the deficits from the Sino-Japanese War and in preparation for the Russo-Japanese War ...
The company has since been taken over by Takeda Pharmaceutical Company. As of 2019[update], a bivalent (NoV GI.1/GII.4) ... A 2006 study found the virus remained on surfaces used for food preparation seven days after contamination. Routine protocols ... "Takeda to Acquire LigoCyte Pharmaceuticals, Inc". Archived from the original on 2013-06-29. Retrieved 2013-06-22. Baehner, F.; ... "Key Products and Pipeline (FY2019 Q2 Pipeline Table)" (PDF). Takeda Pharmaceutical Company. 2019. Archived (PDF) from the ...
In view of Daubert and Kuhmo, the pre trial preparation of expert witnesses is critical. A problem with Daubert is that the ... Merrell Dow Pharmaceuticals (509 U.S. 579 [1993]), General Electric Co. v. Joiner (522 U.S. 136 [1997]), and Kumho Tire Co. v. ...
... and helped to author the Pharmacopoeia Londinensis in 1618-a directory of standardized pharmaceutical preparations given by the ...
Inducing labour can be accomplished with pharmaceutical or non-pharmaceutical methods. Inductions are most often performed ... Psychological preparation may be beneficial. Relaxation techniques, immersion in water, massage, and acupuncture may provide ... Haas, David M.; Morgan, Sarah; Contreras, Karenrose; Kimball, Savannah (26 April 2020). "Vaginal preparation with antiseptic ... preparation, physical environment, pain, immobility, or medical interventions. According to a 2013 analysis performed ...
... which governs the international transactions in drugs and their preparations, does not apply to the preparations in Schedule ... and other psychoactive pharmaceuticals, and the 1988 United Nations Convention Against Illicit Traffic in Narcotic Drugs and ... Schedule III - The preparation, because of the substances which it contains, is not liable to abuse and cannot produce ill ... Schedule III "contains preparations which enjoy a privileged position under the Single Convention, i.e. are subject to a less ...
The next step in the development of e-management was the preparation of the ePoland document, containing an action plan for the ... pharmaceuticals, banking, construction, transport etc.) It also provides other services in respect of already obtained license ... The adoption of this document resulted in the preparation by the Scientific Research Committee of the preliminary concept of ... under preparation). State portal www.e-gov.az was established to facilitate citizens in benefiting from e-services provided by ...
... and pharmaceutical control of its behavior rather than being limited to poorly characterized, expensive, and/or difficult to ... study preparations. Although voltage-gated ion channels are typically activated by membrane depolarization, some channels, such ...
Making various ICT related standards pertaining to various ICT products along with preparation of various GRs, IRs, White ... Department of Pharmaceuticals, Department of Defence, National Highway Authority of India, RITES, IRCON, TCIL, UPSC, SSC, ...
... has granted the United States rights for the ophthalmic preparation to ISTA Pharmaceuticals. In 2011, ISTA pharmaceuticals ... ISTA Pharmaceuticals was acquired by Bausch & Lomb in March 2012 for $500 million. Bausch & Lomb hold the patent for ... It is currently marketed in the United States as an eye drop under the brand-name Bepreve, by ISTA Pharmaceuticals, a ... Blackwell R, Silcoff S, Marotte B (27 May 2013). "Valenant pharmaceuticals eyes China with Bausch deal". The Globe and Mail. ...
"Topical equol preparation improves structural and molecular skin parameters". International Journal of Cosmetic Science. 39 (5 ... Pharmaceutical Biology. 51 (11): 1393-1400. doi:10.3109/13880209.2013.793720. ISSN 1388-0209. PMID 23862588. Magnet, U.; ...
At the time, chronic infectious hepatitis was not known, so when human serum was used in vaccine preparation, serum drawn from ... the French pharmaceutical company. Two other manufacturers supply domestic markets: Wuhan Institute of Biological Products in ... HBV has been available and is routinely used in situations where HBV contamination is possible including vaccine preparation. ...
Pharmaceutical Services and Charges for Drugs and Appliances) Amendment Regulations 1994 (S.I. 1994/2402) County Court ( ... Dangerous Substances and Preparations (Safety) (Consolidation) Regulations 1994 (S.I. 1994/2844) Shetland Islands Council ... General Medical and Pharmaceutical Services) (Scotland) Amendment (No.2) Regulations 1994 (S.I. 1994/2624) Trade Marks (Customs ... General Medical and Pharmaceutical Services) (Scotland) Amendment Regulations 1994 (S.I. 1994/884) European Parliamentary ...
There is evidence from an in vitro study to suggest that the introduction of specific varied preparations containing orlistat, ... Generic orlistat is available in Iran under the brand Venustat manufactured by Aburaihan Pharmaceutical co., in India, under ...
Avoid intravaginal preparations (particularly those that require the use of an applicator) in young girls who are not sexually ... Shen, Tao; Huang, Shile (2016). "Repositioning the Old Fungicide Ciclopirox for New Medical Uses". Current Pharmaceutical ... These topical preparations should not be administered intravaginally and applied in or near the mouth or eyes. In addition, ... Topical preparations containing Naftifine are contraindicated in patients hypersensitive to the drug or any ingredient in the ...
... academic papers have been published by SPU academics on research toward recommended dosages of pharmaceutical preparations, ... Pharmacy in China Pharmaceutical industry in China Shenyang Pharmaceutical University Official Website (in Chinese) Campus real ... It is the first research institute in pharmaceutical sciences in China.[citation needed] Shenyang Pharmaceutical University has ... covering wide and diverse majors in pharmaceutical study. It consists of the schools of Pharmacy, Pharmaceutical engineering, ...
"Ranges of royalty rates, and royalty guidelines, U.S. Pharmaceutical Industry". Archived from the original on 28 September 2007 ... A Guide on the Legal Aspects of the Negotiation and Preparation of Industrial Property Licenses and Technology Transfer ... the pharmaceutical with pre-clinical testing, 2-3% In 2002, the Licensing Economics Review found in a review of 458 licence ... is also feasible when development can be followed stage-wise as shown below for a pharmaceutical undergoing clinical trials ( ...
This is particularly useful in pharmaceutical preparations, e.g. paracetamol. International Union of Pure and Applied Chemistry ... Schiff, Robert (1895-08-09). "Preparation of Thioacetic Acid and its Importance for Chemical-Legal Investigations". Chemical ...
Miller got a sales job at Forest Pharmaceuticals. He enjoyed the job, but after nine months started to miss basketball. After a ... game preparation, player instruction, and on-court coaching. During his first year there, the team won the Horizon League title ...
was sold by Ciba-Geigy AG to the New York-based AEA Investors Inc., in preparation for a subsequent initial public offering. ... The company manufacturers a range of metal detectors for food, pharmaceutical, and non-food applications. To expand the ... in 2015 to become the first manufacturer of instrumentation within the pharmaceutical industry to offer real-time measurement ... The instrumentation provides pure water treatment measurement & control for the pharmaceutical industry; and parameters of ...
... which legally extracts cocaine from coca leaves for use in pharmaceuticals, then sells the processed leaf material for use in ... Coca leaves were used in Coca-Cola's preparation; the small amount of cocaine they contained - along with caffeine originally ...
Royal Pharmaceutical Society of Great Britain. Dept. of Pharmaceutical Sciences (1993). The Extra Pharmacopoeia. Pharmaceutical ... Several long acting injectable preparations are available: several esters of combined estradiol-testosterone, one of estradiol- ... PE3P was developed by the Swedish pharmaceutical company Leo Läkemedel AB in the 1960s. It was introduced for medical use by ... Gynäsan pro injectione)" [Experience with an injectionable estriol Depot preparation. (Gynaesan pro injectione)]. Munch Med ...
It was more active by mouth than other progesterone preparations then on the market, but it was not so active orally as desired ... Progesterone conjugate - Levolta Pharmaceuticals. springer.com Stanczyk FZ (November 2003). "All progestins are not created ... to obtain depot preparations by the method of esterification as in the case of estrogens and androgens. Accordingly, Hohlweg, ...
... though substances which aren't available as commercial pharmaceutical preparations have to be custom prepared by the designated ...
European Pharmaceutical Contractor. No. Autumn. "Formulated Preparations Genearal Monographs: Tablets". British Pharmacopoeia ... Effervescent preparations may enhance absorption and speed up onset of action by increasing gastric pH, therefore hastening the ... There are several categories of active ingredients that may be best administered in the form of effervescent preparations: ... Stahl, Harald (Apr 1, 2003). "Effervescent Dosage Manufacturing". Pharmaceutical Technology Europe. PharmTech. 15 (4). W. A. ...
2009). "Sex hormones and their modulators". Martindale: The Complete Drug Reference (36th ed.). London: Pharmaceutical Press. p ... 375/2 Each tablet of the combined hormone preparation, 'Premenquil', contains 5 mg. of allyloestrenol. [...] Medical ... William Andrew Publishing (22 October 2013). Pharmaceutical Manufacturing Encyclopedia, 3rd Edition. Elsevier. pp. 170-. ISBN ... Indian Journal of Pharmaceutical Sciences. 62 (2): 115. "SuperCYP". Sweetman, Sean C., ed. ( ...
Robson B, Baek OK (2009). The Engines of Hippocrates: From the Dawn of Medicine to Medical and Pharmaceutical Informatics. John ... "Assessment of clinical safety and efficacy in the preparation of Community herbal monographs for well-established and of ... In a 2018 study, FDA identified active pharmaceutical additives in over 700 of analyzed dietary supplements sold as "herbal", " ... In 1972, Tu Youyou, a pharmaceutical chemist, extracted the anti-malarial drug artemisinin from sweet wormwood, a traditional ...
Claimants argue the pharmaceutical manufacturers did not meet a standard of care and were negligent in doing so. These lawsuits ... Pfizer manufactures a preparation of short-acting oxycodone, marketed as Oxecta, which contains inactive ingredients, referred ... These effects make it one of the most commonly abused pharmaceutical drugs in the United States. Diverted oxycodone may be ... The article links Raymond and Arthur Sackler's business practices with the rise of direct pharmaceutical marketing and ...
... (INN; trade name Mildronate, among others) is a limited-market pharmaceutical, developed in 1970 by Ivars Kalviņš at ... Meldonium is believed to continually train the heart pharmacologically, even without physical activity, inducing preparation of ... Meldonium is manufactured by Grindeks, a Latvian pharmaceutical company, with offices in thirteen Eastern European countries as ... and that the decision aimed to remove Eastern European athletes from competitions and his drug from the pharmaceutical market. ...
1966)‎. Quality control of pharmaceutical preparations. World Health Organization. https://apps.who.int/iris/handle/10665/89198 ...
JavaScript is disabled for your browser. Some features of this site may not work without it ...
1967)‎. Quality control of pharmaceutical preparations. World Health Organization. https://extranet.who.int/iris/restricted/ ...
This article was published in the January/February 2016 edition of Pharmaceutical Engineering® Magazine. It is one of five ... A pharmaceutical drug manufacturer was observing air-liquid interface "rings" in several blend tanks (Figure 6). The rings ... 2 a b Lopolito, P. "Case Study: Cleaning and Passivation of Buffer Preparation Tanks." Presented at the Cleaning Validation and ... Unfortunately, due to the high mixing rates used in media and buffer preparation tanks, 316L stainless steel floats are not a ...
Understanding the different microbial contamination risk levels involved in compounding sterile preparations, how to ... Pharmaceutical Compounding-Sterile Preparations is to prevent patient harm and fatalities that may result from nonsterility, ... Pharmaceutical Compounding--Sterile Preparations, Part 3: Risk Levels. Allen Loyd V Jr, Okeke Claudia C Sep/Oct 2007. 404-410. ... Pharmaceutical Compounding--Sterile Preparations, Part 6: 2008 Revisions to Chapter Allen Loyd V Jr, Okeke Claudia C Mar/Apr ...
... a pharmaceutical composition containing the liposome, a preparation thereof, and the use thereof, belonging to the field of ... a preparation method therefor, a liposome containing the pegylated lipid, ... EN) PEGYLATED LIPID, LIPOSOME MODIFIED THEREBY, PHARMACEUTICAL COMPOSITION CONTAINING LIPOSOME, PREPARATION THEREOF, AND USE ... PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES. 9. Medicinal preparations characterised by special physical form. 10. ...
US-5824670-A chemical patent summary.
Determination of Water Vapor Transmission Capacity of Pharmaceutical Packaging Materials. Headspace Gas Analysis for ...
Justia Patents US Patent for 2,4-Diamino 5-bromo 6-chloro pyrimidines, process for their preparation and use as pharmaceuticals ... A pharmaceutical preparation in unit dosage form adapted for administration to obtain anti-ulcer activity comprising per unit ... Hydrophilic copolymers, their preparation and their use in separation techniques * Terpenophenoxyalkylamines and pharmaceutical ... 2,4-Diamino 5-bromo 6-chloro pyrimidines, process for their preparation and use as pharmaceuticals ...
... directory of Barbituric Acid Pharmaceutical Preparations, best deals & rates Barbituric Acid Pharmaceutical Preparations. Shop ... supplies Barbituric Acid Pharmaceutical Preparations businesses, with contact details, address & phone numbers, get best deals ... for Barbituric Acid Pharmaceutical Preparations in Owensboro (KY) at owensboroonline. ... Find Barbituric Acid Pharmaceutical Preparations in Owensboro (KY) - ...
Contains annual data for pharmaceutical preparations except biologicals produced in the United States. ...
The NGS sample preparation market is projected to reach USD 2.7 billion by 2024, at a CAGR of 18.7%. Report provides crucial ... NGS Sample Preparation Market, By End User. *Academic Institutes and Research Centers *Hospitals & Clinics *Pharmaceutical & ... NGS sample preparation Market and Top End-users. Top End-Users in NGS sample preparation Market are:. *Academic Institutes and ... 4.1 NGS Sample Preparation: Market Overview 4.2 NGS Sample Preparation Market Share, By Product, 2018 4.3 Market, By End User, ...
Results of search for su:{Pharmaceutical Preparations} Refine your search. *. Availability. * Limit to currently available ... Pharmaceutical chemicals in perspective / Bryan G. Reuben, Harold A. Wittcoff. by Reuben, Bryan G , Wittcoff, Harold A. ... The future of pharmaceuticals : the changing environment for new drugs / Clement Bezold. by Bezold, Clement. ... The Contribution of acute toxicity testing to the evaluation of pharmaceuticals / edited by D. Schuppan, A. D. Dayan and F. A. ...
Mathur GP, Mathur S, Bhushan V, Gupta V. Alcohol in liquid pharmaceutical preparations--harmful for children. Indian Pediatrics ...
Results of search for ccl=su:{Pharmaceutical preparations.} Refine your search. *. Availability. * Limit to currently ... The quality control of pharmaceutical preparations : report on a European Technical Meeting, Warsaw, 29 May - 2 June 1961. by ... Use of specifications for pharmaceutical preparations : report of a study group [meeting held in Geneva from 4 to 8 December ... by WHO Study Group on the Use of Specifications for Pharmaceutical Preparations , World Health Organization. ...
Chemical Drug Preparations. Liver Disease Drug. Antitumor & Auxiliary Drugs. Nutrition Preparation. Contrast Agent. ... Copyright2015 Cisen Pharmaceutical Co., Ltd. All rights reserved. 鲁ICP备14017151号 SP Design ...
Pharmaceutical preparations. *Patient-care equipment (e.g., ventilators) (This item is included in the table under the ... Membrane filtration in pharmaceutical applications is intended to ensure the microbial quality of polished product water. ... equipment and processes used to purify water for the preparation of concentrates and dialysate and the reprocessing of ... On-line hemofiltration and hemodiafiltration systems use sequential ultrafiltration as the final step in the preparation of ...
Construction and Optimization of Selective Membrane Electrodes for Determination of Doxepin Hydrochloride in Pharmaceutical ... This conclusion is justified by the results obtained from the analysis of pharmaceutical preparations, for which precise and ... was tested by repeating the proposed method for determination of the investigated drug in its pharmaceutical preparations to ... The constructed electrode was preconditioned after preparation by soaking for at least 24 h in 1 × 10 -3 M doxepin ...
Jiangsu Nhwa Pharmaceutical Co., Ltd. mainly produces the central nervous system medication, the strategic positioning in the ... Jiangsu Nhwa Pharmaceutical Co., Ltd. mainly produces the central nervous system medication, the strategic positioning in the ... Jiangsu Nhwa Pharmaceutical Co., Ltd. mainly produces the central nervous system medication, the strategic positioning in the ... Nhwa has large scale pharmaceutical GMP production bases. Nhwa mainly focuses on the production and sales of central nervous ...
Pharmaceutical Preparation Manufacturing services in the MetroWest area ... Pharmaceutical Preparation Manufacturing Pharmacies and Drug Stores Pies Plastic Product Manufacturing Plastics Bottle ... Toilet Preparation Manufacturing Toy Tractor Trailer Transmission and Distribution Transportation Equipment Manufacturing ... Site Preparation Contractors Small Electrical Appliance Manufacturing Soap and Other Detergent Manufacturing Solar Electric ...
... Karakteristike savremenih ... Primorac M, Đorđević L, Vasiljević D. Characteristics of novel pharmaceutical preparations for hormone replacement therapy in ... Primorac, M., Đorđević, L.,& Vasiljević, D.. (2005). Characteristics of novel pharmaceutical preparations for hormone ... Primorac, Marija, Đorđević, Ljiljana, Vasiljević, Dragana, "Characteristics of novel pharmaceutical preparations for hormone ...
What are the pharmaceutical uses of suspensions. Answered By: Walter Simmons Date: created: Oct 25 2022 ... The medical syrup or pharmaceutical syrup is actually used as a vehicle for medicine. It is usually used as a flavored vehicle ... How do you get a pharmaceutical suspension. Answered By: Walter Griffin Date: created: Sep 10 2021 ... Suspensions have been or are used in the following pharmaceutical products and processes: ...
Zenkins Pharmaceuticals is a MSME Pharma company that brings you a complete world of authentic medicare along with wide range ... Zenkins Pharmaceutical Pvt ltd. VPO Khudda Khurd Ambala Jagadhri road Ambala cantt, HARYANA (INDIA) ...
Pharmaceutical Preparations [‎1]‎. Primary Health Care [‎5]‎. Public Health [‎1]‎. Regional Health Planning [‎2]‎. ...
... high-performance liquid chromatographic method is developed for the determination of anagrelide in pharmaceutical preparations ... A VALIDATED HPLC METHOD FOR THE DETERMINATION OF ANAGRELIDE IN PHARMACEUTICAL PREPARATIONS. S. Ramanjaneyulu, A. Durga Vyshnavi ... rugged and useful for the quality control of anagrelide in pharmaceutical preparations. ... high-performance liquid chromatographic method is developed for the determination of anagrelide in pharmaceutical preparations ...
Pharmaceutical compounding-sterile preparations. Rockville (MD): US Pharmacopeial Convention; 2012. p. 350-87. ... Safe preparation and administration of intravitreal bevacizumab injections. N Engl J Med. 2011;365:2238. DOIPubMedGoogle ... practices did not conform to United States Pharmacopeial Convention Chapter 797 standards for compounding sterile preparations ...
An information profile on the potential occupational hazards in the pharmaceutical industry (SIC-2831, SIC-2833, SIC-2834) is ... Pharmaceutical-preparations; Biological-effects; Pathological-effects; Chemical-factory-workers ... An information profile on the potential occupational hazards in the pharmaceutical industry (SIC-2831, SIC-2833, SIC-2834) is ... NIOSH-Contract; Contract-210-77-0167; Pharmaceutical-chemicals; Industrial-processes; Biological-products; ...
Jiangbei Pharmaceutical is located at beautiful north shore of Jiaojiang and east shore of East China Sea. Our company develops ... Zhejiang Jiangbei Pharmaceutical Co., Ltd. Copyright(C)2016 Supported by Toocle Copyright Notice 中文版 ... Jiangbei Pharmaceutical always adhere to the "safety first, prevention first, comprehensive management" of production safety ...
... From this page you can access all of ... Read Handbook Of Extemporaneous Preparation A Guide To Pharmaceutical Compounding 2010. by Jessica 5 ...
  • Croatia - Producer prices in industry: Manufacture of basic pharmaceutical products and pharmaceutical preparations was 107.20 points in October of 2022, according to the EUROSTAT. (cloudfront.net)
  • Trading Economics provides the current actual value, an historical data chart and related indicators for Croatia - Producer prices in industry: Manufacture of basic pharmaceutical products and pharmaceutical preparations - last updated from the EUROSTAT on December of 2022. (cloudfront.net)
  • On Friday, Mochida Pharmaceutical Co Ltd (4534:DEU) closed at 23.60, 13.46% above the 52 week low of 20.80 set on Nov 08, 2022. (ft.com)
  • Ont été inclus tous les patients reçus en consultation ORL ayant déclaré avoir utilisé des substances actives sans prescription médicale pour soulager leur plainte actuelle. (bvsalud.org)
  • regarding the compounding of sterile preparations. (ijpc.com)
  • An information profile on the potential occupational hazards in the pharmaceutical industry (SIC-2831, SIC-2833, SIC-2834) is presented. (cdc.gov)
  • The sites of finished pharmaceutical products have 13 biopharmaceutical production lines such as automatic fermentation, separation and purification, sterile separation packed powder injection, and 13 pharmaceutical products production lines such as powder, capsules, tablets, cream, granules, and sterile powder injections. (completepmo.com)
  • These products have helped the company increase its revenue base and market share in the global NGS sample preparation market. (marketsandmarkets.com)
  • Owing to the high-throughput and high sensitivity offered by NGS, coupled with the decreasing cost of sequencing, the adoption of NGS systems and the corresponding use of sample preparation products is expected to increase in hospitals and clinics in the coming years. (marketsandmarkets.com)
  • Jincheng Pharma mainly engaged in the R&D, production and marketing of pharmaceutical intermediates, APIs, finished pharmaceutical products, and general health products, which is the world's largest production and research base of cephalosporins side-chain intermediates and bio-fermentation API Glutathione, domestic well-known manufacturer of anti-infection and gynecological preparations, and has the most abundant cephalosporin antibiotics and gynecology full-life-cycle series products in China. (completepmo.com)
  • We provide pharmaceutical products and health products for more than 30 countries and regions, and more than 3000 domestic medical institutions and chain drugstores, bring health to hundreds of millions of patients every year. (completepmo.com)
  • It has a R&D team of more than 200 people, led by Taishan industry leading talent, focusing on chemical synthesis, synthetic biology and finished pharmaceutical products, etc., and has built 3 National-level Scientific Research Platforms, 5 Provincial-level Scientific Research Platforms, and 6 Provincial-level Enterprise Technology Centers. (completepmo.com)
  • There are 3 manufacturing sites for cephalosporin pharmaceutical intermediates, 2 manufacturing sites for chemical APIs, 2 manufacturing sites for biosynthetic APIs, and 3 manufacturing sites for finished pharmaceutical products. (completepmo.com)
  • In the future, we will continue to aim at high-quality development, with the goal of meeting customer and clinical needs, focus on high-end pharmaceutical and chemical products, high-threshold characteristic APIs and bioactive products, high-level generic drugs and improved new drugs. (completepmo.com)
  • Historically, Croatia - Producer prices in industry: Manufacture of basic pharmaceutical products and pharmaceutical preparations reached a record high of 107.40 points in May of 2020 and a record low of 61.50 points in January of 2003. (cloudfront.net)
  • Federal Supply Schedule Drugs, Pharmaceuticals, & Hematology Related Products contracts are awarded for items such as non-prescription medicated cosmetics, drugs (including generics and over-the-counter), IV delivery systems, nutritional supplements, and soaps & dispensing equipment. (va.gov)
  • 65 I B Drugs, Pharmaceuticals, & Hematology Related Products Schedule solicitation (M5-Q50A-03-R8) is available for download . (va.gov)
  • PCR assays can be used efficiently and in a cost-effective manner to exclude the contamination of pharmaceutical products by the indicator pathogens. (ijpsr.com)
  • Most significantly, in-line analytical measurements enable reliable, repeatable production of high quality pharmaceutical products, batch after batch. (mt.com)
  • This eBooklet highlights different analytical measurement challenges during biopharmaceutical fermentation and explains the value of implementing in-line process analytical equipment to enable reliable, repeatable production of high quality pharmaceutical products, batch after batch. (mt.com)
  • The Pharmaceutical-related segment is engaged in the manufacture, purchase and sale of pharmaceutical products. (ft.com)
  • At this time, there are no routinely available pharmaceutical products that are FDA-approved for the prevention or treatment of COVID-19. (cdc.gov)
  • Educate patients on the serious risks of misusing non-pharmaceutical chloroquine products and other aquarium use chemicals. (cdc.gov)
  • Adverse events related to non-pharmaceutical products can be reported by emailing [email protected] or calling 1-888-InfoFDA (1-888-463-6332). (cdc.gov)
  • Algae and algal products are used as food for humans and animals: about 60 out of the 20000 species of algae described so far are widely used in the food, pharmaceutical and cosmetic industries. (europa.eu)
  • The future of pharmaceuticals : the changing environment for new drugs / Clement Bezold. (who.int)
  • Pharmaceutical drugs / this publication represents the views and expert opinions of an IARC Working Group on the Evaluation of Carcinogenic Risks to Humans which met in Lyon, 17-24 October 1989. (who.int)
  • Licensed, cGMP pharmaceutical manufacturer Investigational new drugs and placebo for clinical trials Manufacture Seromycin? (indianabids.us)
  • Jiangsu Nhwa Pharmaceutical Co., Ltd. mainly produces the central nervous system medication, the strategic positioning in the field of central nervous system drugs market. (nhwa-group.com)
  • At the same time, the company is committed to expanding CMO/CDMO business, actively exploring the field of new drugs, improving the innovation system of the entire-industry-chain, developing new models of pharmaceutical R&D, and striving to build the company into a world-renowned and nationally leading innovative pharmaceutical and health industry group. (completepmo.com)
  • Mochida Pharmaceutical Co Ltd is a Japan-based company principally engaged in the production and sale of drugs. (ft.com)
  • Results of search for 'ccl=su:{Pharmaceutical preparations. (who.int)
  • Discover our selection of all water- and fat-soluble vitamin standards, from analytical standard to pharmaceutical reference standard purity grade for your various applications involving HPLC and GC instruments. (sigmaaldrich.com)
  • The Context of medicines in developing countries : studies in pharmaceutical anthropology / edited by Sjaak van der Geest and Susan Reynolds Whyte. (who.int)
  • Advanced manufacturing technologies such as pharmaceutical continuous manufacturing (PCM) are gaining increasing stakeholder interest for their potential to improve global health by bolstering medicines supply chain resilience. (usp.org)
  • Catalyst Pharmaceuticals is a commercial-stage biopharmaceutical company focused on in-licensing, developing, and commercializing novel medicines for patients living with rare diseases. (stocktitan.net)
  • While buffers are easily cleaned with water (with a few exceptions due to high water solubility), the industry continues to struggle with visible residue at the air-liquid interface on buffer preparation and storage tanks. (ispe.org)
  • It stresses that although in vitro technology continues to develop in an impressive way and expectations are high within the pharmaceutical industry, the potential of prediction process is yet to be fully realized. (nih.gov)
  • As the only company specializing in CNS field in domestic pharmaceutical industry, Nhwa, integrating R&D, production and sales of APIs, has its coverage mainly in anesthesiology, psychiatry, and neurology. (nhwa-group.com)
  • pharmaceutical industry. (cdc.gov)
  • Industrial process - pharmaceutical industry. (cdc.gov)
  • This procedure is applicable for preparation of caustic soda solution used for cleaning of equipment and accessories in pellet section at manufacturing facility of Pharmaceutical Industry. (pharmaguideline.net)
  • Preparation of MFR in Pharmaceutical Industry. (pharmaguideline.net)
  • The company is a burgeoning entire-industry-chain innovative pharmaceutical and health industry group, with international layout and integrating research, manufacturing and marketing. (completepmo.com)
  • ZETA engineers and builds customized aseptic process solutions for the pharmaceutical industry, such as bioreactors and fermentation systems, downstream systems, preparation systems, pure media systems and CIP and SIP systems. (pharmaceutical-technology.com)
  • The programme provides you with a flexible opportunity for high-level research-based training (you will join a research group) and acquire a range of academic skills including research methods, data analysis and writing research reports that will prepare you for PhD-level study or a career in healthcare research, biotech, pharmaceutical industry or with a government or regulatory body. (ucl.ac.uk)
  • This will prepare you for a career in academia or in healthcare research, biotech, the pharmaceutical industry, or with a government or regulatory body. (ucl.ac.uk)
  • Pharmaceutical waters are a multi-functional resource, crossing all disciplines in the pharmaceutical industry. (mt.com)
  • Overall this thesis, constitutes a unique piece of work combining a plethora of characterisation techniques, with novel in silico tools to investigate interfacial phenomena, of high importance in pharmaceutical industry. (bl.uk)
  • He obtained his Ph.D. in pharmaceutical analysis from Bradford University, Bradford, UK in 2001 and now is director of Pharmaceutical Analysis Research Center and Head of Pharmaceutical Chemistry Department. (benthamscience.com)
  • In cosmetology , alginates extracted from Ascophyllum are used as emulsifiers and emulsion stabilizers in creams and lotions, as excipients absorbable by the epidermis, in preparations such as gels, creams, shampoos. (europa.eu)
  • In this study, monoplex and multiplex PCR based assays were developed and compared with standard conventional methods for rapid detection of three specified topical indicator pathogens, Pseudomonas aeruginosa , Staphylococcus aureus and Candida albicans , in nonsterile pharmaceutical preparations. (ijpsr.com)
  • An upper second-class UK Bachelor's degree or higher in chemistry, biochemistry, pharmacy, the pharmaceutical or physical sciences or related fields, or an overseas qualification of an equivalent standard is required. (ucl.ac.uk)
  • With its 17 subsidiaries worldwide and its highly qualified 1,000 employees, ZETA experts design, build and automate pharmaceutical and food Good Manufacturing Practice (GMP)-compliant plants. (pharmaceutical-technology.com)
  • We need to reduce the barriers to adoption of advanced manufacturing technology (AMT) like pharmaceutical continuous manufacturing (PCM). (usp.org)
  • Pharmaceutical continuous manufacturing: What drug makers need to know. (usp.org)
  • Geographic concentration of pharmaceutical manufacturing: USP Medicine Supply Map an. (usp.org)
  • Automatic equipment for manufacturing tablets tablet press in pharmaceutical production Pharma-Manager.com Online video of production and laboratory equipment from leading. (pharma-manager.com)
  • She has more than 25 years of research experience in the field of pharmaceutical sciences. (benthamscience.com)
  • This programme has a large research component, and you will spend at least ten months of the year conducting an in-depth and novel research project, at the forefront of research in the area of medication safety and/or pharmaceutical sciences in a department or laboratory of your choice. (ucl.ac.uk)
  • M.S. in Pharmaceutical Sciences is a two-year graduate program in one of three unique areas of emphasis: (1) Molecular Medicine and Pharmacogenomics centering on drug discovery principles, (2) Drug Development (Pharmaceutics) focusing on drug delivery to the desired target, or (3) Social and Administrative Pharmacy concerned with the interface between pharmacy and society (concerned with pharmacy outcomes). (nova.edu)
  • Pharmaceutical impurities can be classified as organic or inorganic and include residual solvents. (usp.org)
  • This article will review the different types of buffers, provide approaches to investigate the best cleaning procedure using laboratory testing, and detail strategies for cleaning air-liquid interface residues within buffer preparation and storage tanks. (ispe.org)
  • Common challenges with cleaning buffer preparation tanks are the bands of residue found along air-liquid interfaces. (ispe.org)
  • IMSEAR at SEARO: Alcohol in liquid pharmaceutical preparations--harmful for children. (who.int)
  • Mathur GP, Mathur S, Bhushan V, Gupta V. Alcohol in liquid pharmaceutical preparations--harmful for children. (who.int)
  • Several methods for its determination, both in body fluids and pharmaceuticals, including high performance liquid chromatography, 2 - 4 liquid chromatography coupled with mass spectrometry, 5 - 7 gas chromatography, 8 gas chromatography coupled with mass spectrometry, 9 Thin layer chromatography, 10 potentiometry. (kpubs.org)
  • A reversed-phase high-performance liquid chromatographic method is developed for the determination of anagrelide in pharmaceutical preparations. (pharmascholars.com)
  • Included here are materials used in the preparation and/or formulation of the finished dosage form. (bvsalud.org)
  • Overview of applications, presentations, technical articles, posters or practical manuals using GC and GCMS systems from 2019 - 2020 in the field of pharmaceutical analysis. (labrulez.com)
  • Pharmaceutical chemicals in perspective / Bryan G. Reuben, Harold A. Wittcoff. (who.int)
  • The company has a broad product portfolio including the library preparation, target enrichment, and quality control, which is an important factor for its future growth. (marketsandmarkets.com)
  • Interfacial phenomena are of crucial importance in both pharmaceutical process development and drug product development. (bl.uk)
  • It highlights the importance of fundamental notions of surface thermodynamics in the development of an in-depth understanding of interfacial phenomena and it reveals the prospects of IGC as a potential game changer in pharmaceutical process development and drug product development. (bl.uk)
  • Inappropriate uses include taking commercially available non-pharmaceutical preparations, taking chloroquine phosphate or hydroxychloroquine sulfate without a prescription, and taking additional doses not recommended by a healthcare provider. (cdc.gov)
  • Stainless steel storage tanks are used to store liquids for the beverage, chemical, cosmetic, dairy, food and pharmaceutical industries. (jinzongmachinery.com)
  • The scope, major implications, preparations, general description of regulation contents and acceptable environments are covered. (ijpc.com)
  • RMM ARE increasingly becoming popular in the pharmaceutical, clinical, agricultural, food and processing sectors. (europeanpharmaceuticalreview.com)
  • Our analytical standards of proteins, peptides, and amino acids offer accurate and reliable results in biomarker discovery, pharmaceutical research, clinical and diagnostic testing, top-down and bottom-up proteomics, and food authentication applications. (sigmaaldrich.com)
  • For every stage of the manufacture of pharmaceuticals, METTLER TOLEDO in-line measurement systems deliver accurate, real-time evaluation of process conditions. (mt.com)
  • Catalyst Pharmaceuticals is a commercial-stage biopharmaceutical company focused on developing and commercializing innovative therapies for people with rare debilitating, chronic neuromuscular and neurological diseases, including Lambert-Eaton myasthenic syndrome (LEMS), anti-MuSK antibody positive myasthenia gravis (MuSK-MG) and other neurological and neuromuscular disorders. (stocktitan.net)
  • These compounds may be used in pharmaceutical compositions. (justia.com)
  • The company s end users include leading genomic research centers, government laboratories, academic institutions, pharmaceutical and biotechnology companies, and hospitals, among others. (marketsandmarkets.com)
  • The company has established long-term cooperative relationships with hundreds of pharmaceutical companies around the world, and has formed a global market layout with the domestic market as the main body, Europe, America and India market as the leading exporters, and extending to the markets of Japan, South Korea and ASEAN. (completepmo.com)
  • Looking for business intelligence data on H.W. Naylor Company or other suppliers of Pharmaceuticals? (industrynet.com)
  • Salix is a specialty pharmaceutical company that offers innovative treatments for gastrointestinal (GI) diseases and other disorders. (salix.com)
  • But as Affymetrix competitors Agilent and Motorola still use Incyte's content for their arrays, the Palo Alto genomics and pharmaceutical company was still a thorn in Affymetrix's side. (genomeweb.com)
  • Indeed, as Incyte has indicated that it intends to head in the same direction that Hyseq is moving into - pharmaceutical development, the company will now have the flexibility to use Affymetrix chips in addition to its own internally produced cDNA or oligo chips - a step that could save time and manpower costs. (genomeweb.com)
  • The Centers for Disease Control and Prevention (CDC) has become aware of two individuals who ingested non-pharmaceutical chloroquine phosphate, a chemical for aquarium use that is commercially available for purchase at stores and through internet websites. (cdc.gov)
  • Microfluidics International Corporation, the manufacturer of Microfluidizer® high shear fluid processors, is a leader in the design and production of laboratory and commercial processing equipment used in the production of micro- and nano-scale materials for pharmaceutical, biotech, chemical and diverse industries. (dksh.com)
  • The results obtained by the proposed electrodes were also applied successfully to the determination of the drug in pharmaceutical preparations and biological fluids. (kpubs.org)
  • 11 This work describes new selective membrane sensors, of three types: plastic membrane, coated wire and coated graphite electrodes for the determination of doxepin hydrochloride in pure solutions, pharmaceutical preparations and biological fluids. (kpubs.org)
  • In this humanitarian setting, we reviewed the implementation process and the contribution of temperature screening and handwashing practice at points of entry as part of non-pharmaceutical interventions against COVID-19. (bvsalud.org)
  • Public health actions at this time may focus on the use of appropriate non-pharmaceutical interventions in the community (e.g. school and child-care facility closures , social distancing ), as well the use of medications (e.g. antivirals ) and vaccines, if available. (cdc.gov)
  • Public health actions include continued vaccination, monitoring of pandemic influenza A virus circulation and illness, and reducing the use of non-pharmaceutical interventions in the community (e.g. school closures ). (cdc.gov)
  • The Contribution of acute toxicity testing to the evaluation of pharmaceuticals / edited by D. Schuppan, A. D. Dayan and F. A. Charlesworth. (who.int)
  • Notable progress has been made in methods that encourage the use of PCR as a rapid and accurate tool in quality evaluation of pharmaceuticals. (ijpsr.com)
  • Thus, PCR assays provide specific, reliable results that can be incorporated in quality evaluation of pharmaceuticals and will impact positively in terms of cost and time. (ijpsr.com)
  • Nhwa has large scale pharmaceutical GMP production bases. (nhwa-group.com)
  • Adverse events related to pharmaceuticals can be reported to the FDA MedWatch program ( https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program external icon ). (cdc.gov)
  • Clinicians and public health officials should discourage the public from misusing non-pharmaceutical chloroquine phosphate (a chemical used in home aquariums). (cdc.gov)
  • Pharmaceutical chloroquine phosphate and hydroxychloroquine sulfate are approved by the US Food and Drug Administration (FDA) to treat specific medical conditions, such as malaria, lupus, and rheumatoid arthritis. (cdc.gov)
  • The method was validated and it was concluded that the developed method was accurate, sensitive, precise, rugged and useful for the quality control of anagrelide in pharmaceutical preparations. (pharmascholars.com)
  • 2. In pursuit of preparation of pharmaceutical process quality, it is our responsibility to create a highly efficient lifestyle for our customers. (jinzongmachinery.com)
  • Our provided Jinzong Machinery preparation of pharmaceutical process is prepared using premium quality raw materials. (jinzongmachinery.com)
  • 5 Profile of a Quality Control Laboratory for Pharmaceutical Units. (saujanyabooks.com)
  • Various enterprises, especially pharmaceutical companies and food industries, have been adopting RMM as they have demonstrated improved testing quality and generated considerable savings for businesses. (europeanpharmaceuticalreview.com)
  • Automatic equipment for powder pelletizing by pressing through a sieve in pharmaceutical production Pharma-Manager.com Online video of production and laboratory. (pharma-manager.com)
  • Automatic fluidized bed drying and granulation equipment in pharmaceutical production Pharma-Manager.com Online video of production and laboratory equipment from leading. (pharma-manager.com)
  • Agilent - holds a significant share of the NGS sample preparation market. (marketsandmarkets.com)
  • Experimental and in silico studies are deployed to reveal the importance of sample preparation in the accuracy of IGC measurements. (bl.uk)
  • In the suite Incyte alleged that Affymetrix recommended that its customers to use this amplification method in their standard sample preparation. (genomeweb.com)