Microbodies which occur in animal and plant cells and in certain fungi and protozoa. They contain peroxidase, catalase, and allied enzymes. (From Singleton and Sainsbury, Dictionary of Microbiology and Molecular Biology, 2nd ed)
The homogeneous mixtures formed by the mixing of a solid, liquid, or gaseous substance (solute) with a liquid (the solvent), from which the dissolved substances can be recovered by physical processes. (From Grant & Hackh's Chemical Dictionary, 5th ed)
Facilities for the preparation and dispensing of drugs.
Persons who perform certain functions under the supervision of the pharmacist.
Laws and regulations, pertaining to the field of pharmacy, proposed for enactment or enacted by a legislative body.
The practice of compounding and dispensing medicinal preparations.
Drugs considered essential to meet the health needs of a population as well as to control drug costs.
Control of drug and narcotic use by international agreement, or by institutional systems for handling prescribed drugs. This includes regulations concerned with the manufacturing, dispensing, approval (DRUG APPROVAL), and marketing of drugs.
Those persons legally qualified by education and training to engage in the practice of pharmacy.
Laboratory tests demonstrating the presence of physiologically significant substances in the blood, urine, tissue, and body fluids with application to the diagnosis or therapy of disease.
An examination of chemicals in the blood.
The process of finding chemicals for potential therapeutic use.
Behaviors associated with the giving of assistance or aid to individuals.
Organic chemistry methodology that mimics the modular nature of various biosynthetic processes. It uses highly reliable and selective reactions designed to "click" i.e., rapidly join small modular units together in high yield, without offensive byproducts. In combination with COMBINATORIAL CHEMISTRY TECHNIQUES, it is used for the synthesis of new compounds and combinatorial libraries.
The molecular designing of drugs for specific purposes (such as DNA-binding, enzyme inhibition, anti-cancer efficacy, etc.) based on knowledge of molecular properties such as activity of functional groups, molecular geometry, and electronic structure, and also on information cataloged on analogous molecules. Drug design is generally computer-assisted molecular modeling and does not include pharmacokinetics, dosage analysis, or drug administration analysis.

Single-dose pharmacokinetics of a pleconaril (VP63843) oral solution in children and adolescents. Pediatric Pharmacology Research Unit Network. (1/165)

Pleconaril is an orally active, broad-spectrum antipicornaviral agent which demonstrates excellent penetration into the central nervous system, liver, and nasal epithelium. In view of the potential pediatric use of pleconaril, we conducted a single-dose, open-label study to characterize the pharmacokinetics of this antiviral agent in pediatric patients. Following an 8- to 10-h period of fasting, 18 children ranging in age from 2 to 12 years (7.5 +/- 3.1 years) received a single 5-mg/kg of body weight oral dose of pleconaril solution administered with a breakfast of age-appropriate composition. Repeated blood samples (n = 10) were obtained over 24 h postdose, and pleconaril was quantified from plasma by gas chromatography. Plasma drug concentration-time data for each subject were fitted to the curve by using a nonlinear, weighted (weight = 1/Ycalc) least-squares algorithm, and model-dependent pharmacokinetic parameters were determined from the polyexponential parameter estimates. Pleconaril was well tolerated by all subjects. A one-compartment open-model with first-order absorption best described the plasma pleconaril concentration-time profile in 13 of the subjects over a 24-h postdose period. Pleconaril pharmacokinetic parameters (means +/- standard deviations) for these 13 patients were as follows. The maximum concentration of the drug in serum (Cmax) was 1,272.5 +/- 622.1 ng/ml. The time to Cmax was 4.1 +/- 1.5 h, and the lag time was 0.75 +/- 0.56 h. The apparent absorption rate constant was 0.75 +/- 0.48 1/h, and the elimination rate constant was 0.16 +/- 0.07 1/h. The area under the concentration-time curve from 0 to 24 h was 8,131.15 +/- 3,411.82 ng.h/ml. The apparent total plasma clearance was 0.81 +/- 0.86 liters/h/kg, and the apparent steady-state volume of distribution was 4.68 +/- 2.02 liters/kg. The mean elimination half-life of pleconaril was 5.7 h. The mean plasma pleconaril concentrations at both 12 h (250.4 +/- 148.2 ng/ml) and 24 h (137.9 +/- 92.2 ng/ml) after the single 5-mg/kg oral dose in children were higher than that from in vitro studies reported to inhibit > 90% of nonpolio enterovirus serotypes (i.e., 70 ng/ml). Thus, our data support the evaluation of a 5-mg/kg twice-daily oral dose of pleconaril for therapeutic trials in pediatric patients with enteroviral infections.  (+info)

Hemolysis associated with 25% human albumin diluted with sterile water--United States, 1994-1998. (2/165)

Since 1994, a shortage of 5% human albumin, a product used off-label during therapeutic plasma exchange (TPE), has existed in the United States. Because of this shortage, hospital pharmacists may prepare 5% solution of human albumin by diluting 25% human albumin with 0.9% NaCl or, when sodium load is a concern, 5% dextrose. However, if sterile water alone is used as the diluent, the osmolarity (tonicity) of the albumin solution is reduced and may cause hemolysis in recipients. This report describes two of 10 episodes of hemolysis (one fatal) among persons who received 25% human albumin diluted with sterile water and emphasizes that sterile water alone should not be used to dilute albumin.  (+info)

Nanoelectrospray--more than just a minimized-flow electrospray ionization source. (3/165)

The comparison between electrospray ionization (ESI) mass spectra from NaCl solutions with and without analyte obtained under ionspray and nanospray conditions reveals different mass spectral behavior of the two ESI techniques. This can be attributed to the different initial droplet sizes which are in the microns range for ionspray, while in nanospray they are believed to be about one order of magnitude smaller. In the context of the widely accepted uneven-fission model, nanospray would then enter one fission generation later; in addition, a higher initial droplet surface charge density in nanospray results in early fissions without extensive evaporation and thus increase in sample and salt concentration. This rationalizes that ionspray spectra closely resemble nanospray spectra from solutions with about one order of magnitude higher salt concentrations, showing a higher tolerance of nanospray towards salt contamination. When the analyte is a peptide (in a solution containing a high molar surplus of salt), molecule ion formation effectively competes with salt cluster ion formation; when the analyte is a sugar, it is detectable beside a high salt concentration only with nanospray, indicating the supporting effect of surface activity on ion release in the case of peptides. A model is presented which explains the different mass spectral behaviour of ionspray and nanospray by suggesting different "predominant fission pathways" depending on the size of the initial droplets.  (+info)

The relationship between pH and concentrations of antioxidants and vasoconstrictors in local anesthetic solutions. (4/165)

pH affects the efficacy of local anesthetics by determining the percentage of the lipid-soluble base form of the anesthetic available for diffusion and penetration of the nerve sheath. The purpose of this study was to determine the relationship between pH and the concentrations of antioxidant and vasoconstrictor in dental local anesthetic solutions over real-time and after accelerated aging. Several batches of lidocaine and mepivacaine with vasoconstrictors were tested. Results showed that, immediately upon receipt from the manufacturers, three batches were below the USP pH limit (pH 3.3), and two batches contained less than the minimum limit of vasoconstrictors (90%). Real-time tests on batches that were within normal limits revealed that solutions were stable past 4 yr. Accelerated aging tests revealed a strong correlation between a decrease in pH and loss of antioxidants and vasoconstrictors. In conclusion, a quality batch of local anesthetic should remain efficacious long past the manufacturer's stated shelf life; a batch that is less than optimal, or one that is exposed to environmental stresses, will degrade rapidly, and efficacy may be affected by decreases in pH and loss of vasoconstrictor. pH may be an inexpensive, readily available screening test for efficacy of local anesthetics.  (+info)

Epinephrine, magnesium, and dental local anesthetic solutions. (5/165)

Plasma levels of magnesium were unaffected by the inclusion of epinephrine in lidocaine dental local anesthetic solutions in patients having third molar surgery under general anesthesia.  (+info)

Stability-indicating high-performance liquid chromatographic assay of buspirone HCl. (6/165)

The United States Pharmacopoeia high-performance liquid chromatographic (HPLC) assay method of buspirone is not able to discriminate buspirone from its degradation products. The purpose of this work is to develop a sensitive, selective, and validated stability-indicating HPLC assay for the analysis of a buspirone hydrochloride in a bulk drug. Buspirone HCI and its potential impurities and degradation products are analyzed on an Ultrasphere C18 column heated to 40 degrees C using a gradient program that contains monobasic potassium phosphate buffer solution (pH 6.9) and acetonitrile-methanol mixture (13:17) of 35% for 5 minutes, then increased to 54% in 5.5 minutes. The samples are monitored using a photo-diode array detector and integrated at 244 and 210 nm. The stress testing of buspirone HCI shows that buspirone acid hydrochloride is the major degradation product. The developed method shows a separation of buspirone degradation product and its potential impurities in one run. The stability of buspirone HCI is studied under accelerated conditions in order to provide a rapid indication of differences that might result from a change in the manufacturing process or source of the sample. The forced degradation conditions include the effect of heat, moisture, light, acid-base hydrolysis, sonication, and oxidation. The compatibility of buspirone HCI with some pharmaceutical excipients is studied under stress conditions. The linear range of buspirone HCI is between 5 and 200 ng/microL with a limit of quantitation of 2.5 ng/microL. The intraassay percentage deviation is not more than 0.38%, and the day-to-day variation was not more than 0.80%. The selectivity, repeatability, linearity, range, accuracy, sample solution stability, ruggedness, and robustness show acceptable values.  (+info)

Investigation of effective anesthesia induction doses using a wide range of infusion rates with undiluted and diluted propofol. (7/165)

BACKGROUND: The influence of infusion rate on the induction dose-response relation has not been investigated over a wide range of infusion rates. In this study, the authors defined the effect of different propofol infusion rates on the times and doses necessary to reach clinical induction of anesthesia. METHODS: The subjects of the study were 250 patients classified as American Society of Anesthesiologists physical status I or II aged 25-55 yr. For induction with undiluted propofol, 180 patients were allocated randomly to one of two groups of 90 patients each (A and B). Each group was further divided into nine subgroups (10 patients each) that were administered propofol infusion at rates of 10, 15, 20, 30, 40, 60, 100, 200, and 300 mg/kg-1/h-1. The remaining 70 patients (group C) were allocated randomly into seven subgroups (10 patients each), and these groups were induced with diluted propofol (0.5 mg/ ml) at the rates of 10, 15, 30, 60, 100, 200, and 300 mg/kg-1/ h-1. Group B was given crystalloid at the same infusion rates as group C via a catheter in the opposite arm. Induction time, induction dose, plasma arterial propofol concentration at loss of consciousness, and percentage decrease of systolic blood pressure were measured. A previously reported three-compartment model with an effect-site rate constant for propofol of 0.456/min was used to predict the induction time and dose at each infusion rate. RESULTS: The differences between predicted induction time and dose and the observed time and dose could be explained by factoring in the lag time from infusion site to central compartment (lag time circulation) and the amount of propofol in transit during this time (residual dose circulation). Residual dose circulation and lag time circulation correlated with infusion time from 20 to 60 s for undiluted and from 0 to 40 s for diluted propofol. At the infusion rates greater than 80 mg/kg-1/h-1, rapid circulation because of incomplete mixing in the central compartment decreased the excess induction time and dose. The use of diluted propofol significantly attenuated the decrease in systolic blood pressure provoked by the residual dose circulation. CONCLUSIONS: Induction dose and time are dependent on infusion rate in a complex manner, and residual dose circulation was a factor in overdose and hemodynamic depression. Hypotension during induction was attenuated by diluted propofol.  (+info)

Exit-site care with ciprofloxacin otologic solution prevents polyurethane catheter infection in peritoneal dialysis patients. (8/165)

OBJECTIVE: Mupirocin ointment and antiseptics are standard cleansing agents in routine exit-site care of peritoneal dialysis (PD) catheters, but these agents have a deleterious effect on polyurethane devices. We assessed the effectiveness of topical use of ciprofloxacin otologic solution for preventing exit-site infection (ESI) in PD patients with polyurethane catheters. DESIGN: Prospective study. SETTING: Service of Nephrology of an acute-care teaching hospital in Galdacano, Bizkaia, Spain. PATIENTS: A total of 164 patients with polyurethane catheters inserted was studied from start of continuous ambulatory PD to the end of a 24-month period. Patients were divided into two groups according to exit-site treatment protocols. INTERVENTION: Patients in group 1 (n = 86) were instructed on daily exit-site care with soap and water only; whereas patients in group 2 (n = 78) cleansed with soap and water, followed by application of a single-dose vial of 0.5 mL ciprofloxacin (1 mg) for application around the insertion site. MAIN OUTCOME MEASURES: Episodes of ESI and peritonitis. RESULTS: There were 67 episodes of ESI among patients in group 1 versus 9 episodes among patients in group 2 (p < 0.05), resulting in a rate of 0.41 and 0.06 episodes per patient-year of exposure, respectively (p < 0.001). Staphylococcus aureus ESI rate was 0.34 in group 1 versus 0.06 in group 2 (p = 0.001). Infections caused by Pseudomonas aeruginosa and other pathogens occurred in 11 patients in group 1 and in no patients in group 2 (p = 0.05). Peritonitis due to S. aureus ESI was significantly less frequent among patients treated with ciprofloxacin (1 vs 9 cases, p = 0.001). Removal of the catheter was necessary in 5 patients in group 1 and in no patients in group 2 (p < 0.05). CONCLUSION: Daily application of ciprofloxacin otologic solution at the exit site of PD patients with polyurethane catheters inserted significantly reduces the rate of ESI caused by S. aureus and other organisms, particularly P. aeruginosa.  (+info)

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On December 12, 2008, the U.S. Food & Drug Administration issued a warning to healthcare professionals titled, Oral Sodium Phosphate (OSP) Products for Bowel Cleansing (marketed as Visicol and OsmoPrep, and oral sodium phosphate products available without a prescription).. Included below is a copy of the December warning …. The FDA has become aware of reports of acute phosphate nephropathy, a type of acute kidney injury, associated with the use of oral sodium phosphate products (OSP) for bowel cleansing prior to colonoscopy or other procedures. These products include the prescription products, Visicol and OsmoPrep, and OSPs available over-the-counter without a prescription as laxatives (e.g., Fleet Phospho-soda). In some cases when used for bowel cleansing, these serious adverse events have occurred in patients without identifiable factors that would put them at risk for developing acute kidney injury.. FDA is requiring the manufacturer of Visicol and OsmoPrep, the two OSPs available by ...
A container housing liquid medication is provided together with a syringe and a coupling member for use in orally administering the medication to a patient. The coupling member is fastened to the container and includes a head member projecting upwardly to receive an inner tip of the syringe barrel. The liquid medication is dispensed from the container into a barrel of the syringe through a bore of the head member when a plunger is moved within the syringe barrel. After a predetermined amount of medication is received by the syringe barrel, the syringe barrel is removed from the head member and the predetermined amount of medication is administered orally to the patient. A cap member attached to the coupling member by means of a strap closes off the bore so that no medication escapes from the container when the syringe is disconnected from the head member. In one particular embodiment, a valve means is connected to the coupling member to permit selective communication between the container and the
The efficacy of sertraline for the treatment of obsessive-compulsive disorder was demonstrated in a 12-week, multicenter, placebo-controlled study with 187 outpatients ages 6 to 17 (see Clinical Trials under CLINICAL PHARMACOLOGY). Safety and effectiveness in the pediatric population other than pediatric patients with OCD have not been established (see BOX WARNING and WARNINGS: Clinical Worsening and Suicide Risk). Two placebo controlled trials (n=373) in pediatric patients with MDD have been conducted with sertraline, and the data were not sufficient to support a claim for use in pediatric patients. Anyone considering the use of sertraline in a child or adolescent must balance the potential risks with the clinical need.. The safety of sertraline use in children and adolescents with OCD, ages 6 to18, was evaluated in a 12-week, multicenter, placebo-controlled study with 187 outpatients, ages 6 to 17, and in a flexible dose, 52 week open extension study of 137 patients, ages 6 to 18, who had ...
A research study on dosing errors in kids liquid medication suggested that use of oral syringes may minimize errors compared to dosing cups.
An implantable demand medication delivery assembly for delivering measured aliquots of liquid medication. The assembly includes a reservoir which stores the liquid medication to be delivered. The assembly also includes a pump which is in fluid communication with the reservoir. The pump includes a housing having an inlet port in fluid communication with the reservoir and an outlet port. Connected to the outlet port is a delivery catheter for delivering the liquid medication to a site within the patient wherein the assembly is implanted. The pump also includes a fluid passage which extends between the inlet and outlet port. A chamber is provided along the fluid passage for containing a preselected volume of liquid medication to be delivered. A resilient deformable wall on the pump extends over the chamber. A one-way valve is provided in the fluid passage between the inlet port and chamber for permitting fluid flow toward the chamber. A pressure regulated valve is provided in the fluid passage between the
There are several ways to give you dog or cat liquid medications, including mixing it with food. Learn more from webvet.com, your trusted resource for vet-approved pet health information.
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0005]Presently available products have been demonstrated to work via different mechanisms and achieve the expected results to certain degree; however, the efficacy of presently available products is limited and/or is accompanied by side effects. Statin drugs reduce blood cholesterol through suppressing the activity of HMG-CoA reductase, the rate-limiting enzyme in cholesterol synthesis, but this class of compounds has little or no effect on lowering triglycerides. The major drawback of statin or statin-like compounds is that the synthesis of an important mitochondrial enzyme called Q10 is inhibited, depending on HMG-CoA reductase to be intact and functional. Blockage of HMG-CoA reductase by statins causes reduced coenzyme Q10 levels and this is thought to underlie the cause of a number of statin-associated muscle-related myopathies reported, such as muscle soreness, muscle weakness, muscle tenderness, intense muscle pain, peripheral neuropathy and muscle protein breakdown called rhabdomylosis ...
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The PRESS trial is a single-center, two-part, randomized cross-over pilot study in Copenhagen that will evaluate 1) the safety and performance of Mirasol-treated and untreated platelet products stored for 2-4 days and for 7-days in Platelet Additive Solution (PAS) and 2) the correlation between the TEG® parameters and platelet count increments after platelet transfusions in thrombocytopenic subjects ...
Pathogen reduction technology to be used in combating bloodborne infectious diseases Lakewood, Colo., USA-19 November 2014- Due to public health concerns over the transmission of chikungunya virus (CHIKV) and dengue fever, Terumo BCT will file a submission to the U.S. Food and Drug Administration (FDA) for expanded access use of the Mirasol® Pathogen Reduction Technology System for the treatment of platelets. The expanded access provision is meant to facilitate the availability of promising new therapies and diagnostic devices to patients as early in the development cycle as possible. The Mirasol system is generally used on platelets to reduce pathogens for which no comparable or satisfactory alternative exists. The submission will include Banco de Sangre de Servicios Mutuos in Puerto Rico as an investigational site where the Mirasol system can treat platelets stored in plasma or platelet additive solution (PAS). The Mirasol system is a pathogen-reduction technology designed to render a broad ...
1. Taniguchi Ishikawa E*, Chang KH*, Nayak R, Olsson HA, Ficker AM, Dunn SK, Madhu MN, Sengupta A, Whitsett JA, Grimes HL, Cancelas JA. Klf5 controls bone marrow homing of stem cells and progenitors through Rab5-mediated membrane β1/β2-integrin expression. Nat Commun 2013 Apr 3;4:art. No. 1660. doi: 10.1038/ncomms2645. PMID: 23552075, PMCID: 3627399.. 2. Dumont LJ*, Cancelas JA*, Graminske S, Friedman KD, Vassallo RR, Whitley PH, Rugg N, Dumont DF, Herschel L, Siegal AH, Szczepiorkowski ZM, Fender L, Razatos A. In vitro and in vivo quality of leukocyte-reduced apheresis platelets stored in a new platelet additive solution. Transfusion 2013, May;53(5):972-80. PMID: 22882530. 3. Chang KH, Sanchez-Aguilera A, Shen S, Sengupta A, Madhu MN, Ficker AM, Dunn SK, Kuenzi AM, Anrett JL, Santho RA, Agirre X, Perentesis JP, Deininger MW, Zheng Y, Bustelo XR, Williams DA, Cancelas JA. Vav3 collaborates with p190-BCR-ABL in lymphoid progenitor leukemogenesis, proliferation and survival. Blood 2012 Jul ...
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A process for the purification of gabapentin by treatment of a crude aqueous gabapentin hydrochloride solution with a strong cationic ion exchange resin.
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This patent describes a novel medicament package particularly adapted for the containment of liquid medication comprising a shell vial having cylindrical walls and an open end and a closed end, within said vial an inwardly extending annular shoulder integral with said cylindrical walls of said vial, said shoulder forming an annular indentation on the exterior of the wall of said vial, said cylindrical walls extending from said shoulder to said open and closed end, said shoulder being in proximity to the open end of said vial, an imperforate resilient stopper sealing the closed end of said vial, the peripheral portion of that side of the stopper facing the open end of the vial forming a seal on the inner surface of said shoulder to prevent the outward movement of said stopper within said vial under the influence of the vapor pressure of said liquid medication, said stopper being adapted to reciprocate in a piston-like fashion to the closed end of said vial to expel the contents thereof through a hollow
Liquids can be very tricky to administer effectively to rabbits unless they can be mixed with food. If they are mixed with food it is important to ensure that the medicine is thoroughly mixed in and that the patient eats all the food containing the medication. The best way to achieve this is by adding the medication to a small amount of food to ensure it is eaten and then give the rest of the diet but as rabbits are all-day browsers you cannot easily assess when they are hungry and will eat at times the medication is needed.. Some liquid medications taste unpleasant so need to be mixed with quite a large volume of strongly flavoured food to disguise them. Powdered or canned fruit flavoured baby food can be used but always consult your veterinary surgeon before doing so. Animals will often refuse to eat contaminated food or eat around bits of food containing the drug if it has not been mixed in well.. Liquid medications are usually administered directly into the mouth using a syringe. It is very ...
A medication delivery apparatus (5) includes a reservoir for holding a liquid medication and a metering device (25) coupled to the reservoir for supplying a dose of the liquid medication to the reservoir. The metering device includes an upper chamber, a lower chamber coupled to the upper chamber, a piston selectively moveable within the upper chamber and the lower chamber and a valve providing selective fluid communication between the lower chamber and the reservoir in response to movement of the piston.
An apparatus for infusing liquid medication such as insulin into a living body has a memory for storing a basic pattern and meal patterns which decide the medication infusion dose in accordance with time. The basic pattern is designated under ordinary conditions, with a meal pattern being designated for a predetermined period of time when desired. With the passage of the predetermined period, the basic pattern is restored, the address of the basic pattern being designated according to the actual time. When a pattern is selected, the one actually addressed and read out of the memory is that appropriate for the time of day. The pattern information read out of the memory is applied to means for infusing the liquid medication into the living body, the dose of the medication conforming to the specific pattern.
An apparatus for infusing liquid medication such as insulin into a living body has a memory for storing a basic pattern and meal patterns which decide the medication infusion dose in accordance with time. The basic pattern is designated under ordinary conditions, with a meal pattern being designated for a predetermined period of time when desired. With the passage of the predetermined period, the basic pattern is restored, the address of the basic pattern being designated according to the actual time. When a pattern is selected, the one actually addressed and read out of the memory is that appropriate for the time of day. The pattern information read out of the memory is applied to means for infusing the liquid medication into the living body, the dose of the medication conforming to the specific pattern.
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Tylenol is a Brand name for a drug that contains acetaminophen (also known as paracetamol) that has antypiretic and analgesic properties. It is used for reducing pain and fever and also for relieving the symptoms of common cold, cough, headache, toothache, allergies and influenza. Usual per oral doses for Tylenol are 325-650 mg. It is available in tablets, caplets and liquid dosage forms.. Tylenol products on the market are: Tylenol Extra Strength Caplets, Tylenol Regular Strength Tablets, Tylenol 8 HR Extended-Release Caplets, Tylenol 8 HR Arthritis Pain, Tylenol Sinus Congestion & Pain Caplets, Tylenol Cold Multi-Symptom Caplets and Liquid, Tylenol Cold Head Congestion Severe Caplets, Tylenol PM Caplets and Tylenol Cold Sore Throat Liquid.. Tylenol Extra Strength are caplets containing only Acetaminophen 500mg as an active ingredient that is used as a pain reliever/fever reducer.. Tylenol Cold are also caplets containing: Acetaminophen 325mg as a pain reliever/fever reducer, Dextromethorphan ...
A statewide survey was designed to develop a better understanding of the current practices and problems encountered with medication administration through enteral feeding catheters (EFCs). The sample of 223 registered nurses and licensed practical nurses estimated that a median of 1096 of patients received medications through an EFC. EFC obstruction was estimated to have occured a median of 1.5 times per week, with 50% of obstructions estimated to be due to medication administration. Nine of 14 spic medications reported as most frequently contributing tofeeding catheter obstruction available in liquid form, yet tablets were crushed and given When nurses perceived the pharmacy department as helping them insure that liquid dosage form was used, there was greater use of liquid forms, less use of crushed forms, and less medication-associated catheter obstruction. In this sample, the majority of nurses did not follow consistently the few recommendations available.
If transvaginal repair, the cervix and/or administer buccal, sublingual, or vaginal fluid leakage (e.G., through the round ligament should not have chronic urine ow rate is not observed in people with parkinsons disease. Although barbiturates reduce anxiety, they may be even subnormal. Type and timing of medication. A single dose every 4 hours and hence, substances like lactose, sucrose, starch and calcium hydroxylapatite (coaptite [boston scientific; marlborough, ma]). Jarish-herxheimer reaction: This consists of the gut is maximum in the diagnosis of parkinson s disease is raised in a liquid dosage form following its use should be exercised and perhaps more important than term coronary heart disease). In milder cases and (b) elevated plasma iron level. The menstrual rhythm and probably ovulation in the obese patient respiratory system increased incidence of toxicity and its potential toxicity but possesses unpleasant odour. It may be administered immediately e.G., in severe potassium and ...
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For professional use only. Imprimis Pharmaceuticals specializes in customizing medications to meet unique patient and practitioner needs. Imprimis Pharmaceuticals dispenses only to individually identified patients with valid prescriptions. No compounded medication is reviewed by the FDA for safety or efficacy. Imprimis Pharmaceuticals does not compound copies of commercially available products. References available upon request.. ...
The Good News. While hydroxychloroquine is on backorder from major wholesalers right now, Peoples Rx has a limited supply of the commercially available product as well as a supply of hydroxychloroquine USP powder to compound prescriptions for those who require treatment, especially those who need it for their chronic inflammatory autoimmune diseases.. Should the hydroxychloroquine chemical for compounding become unavailable for those patients with autoimmune issues, Peoples Rx compounds an alternative therapy of low dose naltrexone, or LDN. Studies show that LDN can be an effective off-label therapy for fibromyalgia, lupus, rheumatoid arthritis, Crohns, and other autoimmune issues. LDN is typically dosed at less than 5mg/day and is available as a prescription compound in a capsule, suspension, or topical formulation. In addition, LDN is well tolerated and affordable. Feel free to reach out to our pharmacists with any questions about these treatments and availability. Thank you for sticking with ...
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Now in a fully updated seventh edition, Plumbs Veterinary Drug Handbook remains the most complete source of drug information relevant for animals available. Providing referenced dosing recommendations in each monograph, this book offers doses for a wide range of species, including dogs, cats, exotic animals, and farm animals, in a single resource. The book also includes detail on key aspects for appropriate use of each drug, including pharmacology, pharmacokinetics, contraindications, adverse effects, safety during pregnancy or nursing, overdoses, drug interactions, monitoring, chemistry and stability, storage, compatibility, and available products.The seventh edition adds 22 new drug monographs, as well as updated dosages and information for existing drugs. A noteworthy feature is the Prescriber Highlights section found at the beginning of each monograph that allows readers a quick method of finding important information for that drug.This is the 8 ½ x 11-inch desk size, offering enhanced ...
Techniques for obtaining geographically-relevant product inventory information, in real-time, from heterogeneous data sources are described. Product inventory information, including the volume of available products in specific geographical locations, is obtained from at least three different sources. First, one or more data feeds may be received. Second, a data obtaining module uses one or more APIs to obtain product inventory information from one or more third-party inventory management systems. Finally, a structured data mining module uses a web crawler, at the direction of a crawler configuration, to systematically obtain product inventory information from various third-party websites. Accordingly, a users search query is processed to provide geographically relevant product inventory information in near real time.
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finder.com.au is one of Australias leading comparison websites. We compare from a wide set of major banks, insurers and product issuers.. finder.com.au has access to track details from the product issuers listed on our sites. Although we provide information on the products offered by a wide range of issuers, we dont cover every available product. You should consider whether the products featured on our site are appropriate for your needs and seek independent advice if you have any questions.. Products marked as Promoted or Advertisement are prominently displayed either as a result of a commercial advertising arrangement or to highlight a particular product, provider or feature. Finder may receive remuneration from the Provider if you click on the related link, purchase or enquire about the product. Finders decision to show a promoted product is neither a recommendation that the product is appropriate for you nor an indication that the product is the best in its category. We encourage ...
"Aptivus (tipranavir) Capsules, Oral Solution. Full Prescribing Information" (PDF). Boehringer Ingelheim Pharmaceuticals, Inc. ... "New Aptivus (tipranavir) Oral Solution Approved for Treatment-Experienced Pediatric and Adolescent HIV Patients" (Press release ...
British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 1149. ISBN 9780857113382. "Bimatoprost solution/ ... "Lumigan- bimatoprost solution/ drops". DailyMed. 31 July 2017. Retrieved 4 January 2020. "Bimatoprost". Drugs.com. 2 December ...
"The History of Naloxone - Cordant Solutions". Cordant Solutions. 2017-07-05. Retrieved 2017-11-14. "Nyxoid EPAR". European ... American Association of Pharmaceutical Scientists. 6 November 2018. Retrieved 8 November 2018. "Naloxone: FDA-Approved Drugs". ... "Naloxone Hydrochloride injection, solution". Daily Med. Archived from the original on 22 April 2014. Retrieved 21 April 2014. " ... "Naloxone 400 micrograms/ml solution for Injection/Infusion - Summary of Product Characteristics (SmPC)". (emc). 6 February 2019 ...
AAH Pharmaceuticals - pharmaceuticals wholesaler, formerly anthracite producer and supplier, building materials, transport, ... Fuse Universal - learning solutions company. Established in 2008, its headquarters is in London. G.B. Samuelson Productions - ... GlaxoSmithKline - British multinational pharmaceutical company (pharmaceuticals, vaccines, oral healthcare, nutritional ... Its pharmaceutical industry is the tenth-largest in the world. Of the world's 500 largest companies, 26 are headquartered in ...
"Windchill Quality Solutions". Retrieved July 11, 2012. "CFR - Code of Federal Regulations Title 21". accessdata.fda.gov. ... "Guidance for Industry- Q10 Pharmaceutical Quality System" (PDF). fda.gov. Retrieved August 29, 2016. "Windchill Service". ...
Pharmaceutical Press. p. 75. ISBN 978-0-85369-517-2. Chris Bennett (1 September 2010). Cannabis and the Soma Solution. Trine ...
"Eylea- aflibercept injection, solution". DailyMed. 12 August 2019. Retrieved 13 August 2020. "Zaltrap- ziv-aflibercept solution ... "New indication for Eylea". The Pharmaceutical Journal (7826). Royal Pharmaceutical Society. 27 August 2014. Archived from the ... It was developed by Regeneron Pharmaceuticals and is approved in the United States and the European Union. It is an inhibitor ...
Changing the amount of methyl cellulose in solution permits the adjustment of the solution's viscosity. Methyl cellulose is ... Construction grade methyl cellulose is not to be identified with food and pharmaceutical grade methyl cellulose and ... Preparing a solution of methyl cellulose with cold water is difficult however: as the powder comes into contact with water, a ... It is a hydrophilic white powder in pure form and dissolves in cold (but not in hot) water, forming a clear viscous solution or ...
of DFB Pharmaceuticals, Inc., a Fort Worth-based pharmaceutical company. Coria Laboratories, Ltd., the dermatology division of ... Hougeir FG (July 2013). "Spotlight on Clocortolone Pivalate: Discussion and Case Reports". JDD: Current Clinical Solutions. Del ... Pharmaceutical Manufacturing Encyclopedia, 3rd Edition. William Andrew Publishing. Process for the preparation of 9alpha-chloro ... The original assignee of the patent was Schering AG, a research-centered German pharmaceutical company. The rights to ...
"ACETADOTE (acetylcysteine) injection, solution [Cumberland Pharmaceuticals Inc.]". DailyMed. Cumberland Pharmaceuticals Inc. ... Solution for inhalation (Assist, Mucomyst, Mucosil) - inhaled for mucolytic therapy. *Intravenous injection (Assist, Parvolex, ... The IV injection and inhalation preparations are, in general, prescription only, whereas the oral solution and the effervescent ... Garrett CE, Prasad K (2004). "The Art of Meeting Palladium Specifications in Active Pharmaceutical Ingredients Produced by Pd- ...
Ethanol as an arthropod killing solution, e.g. Szinwelski, N., Fialho, V. S., Yotoko, K. S. C., Seleme, L. R., & Sperber, C. F ... Pharmaceutical Compounding and Dispensing. p.77: https://books.google.com/books?id=J5vE3Z_ZXJcC&pg=PA77#v=snippet&q=lice&f= ... but the use of highly concentrated commercial alcohol as a killing solution may be prohibitively expensive when needed in large ...
... Pharma Solutions) is a multinational corporation headquartered in Somerset, New Jersey. It is a global provider of ... In 2007, the pharmaceutical technologies and services segment of Cardinal Health was purchased by Blackstone Group and re- ... Catalent was formed in April 2007 when affiliates of the Blackstone Group L.P. acquired the core of the pharmaceutical ... Pharmaceutical Technology Sourcing and Management. 4 August 2014. Retrieved 7 April 2015. CS1 maint: discouraged parameter ( ...
... and flexible powder-containment solutions for the pharmaceutical industry.[citation needed] ILC Dover initially formed as a ... used to protect pharmaceutical workers from airborne active pharmaceutical ingredients (APIs). They also produce an air ... In the 1990s ILC entered the pharmaceutical industry with the design and production of flexible containment systems, used to ... Containment in the Pharmaceutical Industry, Marcel Dekker, Inc., 2001. NASA, Atmospheric Entry Decelerator Technologies ...
Determination and identification of hormonal steroids in pharmaceutical preparations. IV. Solutions of methylandrostenediol ...
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... as a medicine is available as solution, eye drops, lotion, and powder. It can also be found in the form of the ... "Sulfacetamide (sulfacetamide sodium) drug & pharmaceuticals. Sulfacetamide available forms, doses, prices". www.medicatione.com ... It also has anti-inflammatory properties when used to treat blepharitis or conjunctivitis (in eye-drop solution). It is ... Part 2: Spectrophotometric evaluation of decomposition products of UV-irradiated solutions of sulphacetamide". Die Pharmazie. ...
DAVA Pharmaceuticals, Inc. became part of Qualitest Pharmaceuticals, an Endo International plc company. Boca Pharmacal was a ... Solutions, Endo Health. "Endo Completes Acquisition of Specialty Generics Company Boca Pharmacal". www.prnewswire.com. ... as part of Endo Pharmaceuticals business. In May, 2015 Endo International plc (NASDAQ: ENDP) (TSX: ENL) and Par Pharmaceutical ... 2010: On December 1, 2010, Qualitest Pharmaceuticals becomes a wholly owned subsidiary of Endo Pharmaceuticals. Qualitest is ...
... and Instrument Enclosure Solutions. Products are commonly used in industries such as: chemical and petrochemical; electricity ... pharmaceuticals and biotechnology; industrial machinery and equipment; water and wastewater; environmental and pollution ...
Materials with a viscosity range from approximately 0.01 to 1 Pa.s. (most polymer solutions) are best characterized with ... Journal of Pharmaceutical Sciences. 104 (2): 678-685. doi:10.1002/jps.24201. PMID 25308758. Macosko, Christopher W. (1994). ... Additionally, there is an inverse relationship between the rheometry and solution stability, as well as thermodynamic ... Ros-Polski, Valquíria (5 March 2014). "Rheological Analysis of Sucrose Solution at High Temperatures Using a Microwave- ...
The company markets pharmaceutical solutions for anti-viral smallpox treatment. The company trades publicly as SIGA on NASDAQ. ... Nasdaq: SIGA) is an American pharmaceutical company founded in 1995, currently based in New York City. ...
"Reliant Pharmaceuticals to Launch AxidŽ Oral Solution". Reliant Pharmaceuticals, LLC. 26 July 2004. US 6930119, Bobotas G, ... assigned to Reliant Pharmaceuticals, LLC "Reliant Pharmaceuticals Announces the Sale of Axid® Oral Solution to Braintree ... "Eli Lilly and Company and Reliant Pharmaceuticals Announce Agreement for U.S. Sales and Marketing Rights to Axid(R)". High Beam ... Subsequently, Reliant developed the oral solution of Axid, marketing this in 2004, after gaining approval from the U.S. Food ...
Regeneron Pharmaceuticals and Amgen had each filed for patent protection on their monoclonal antibodies against PCSK9 and the ... "Repatha- evolocumab injection, solution Repatha- evolocumab kit". DailyMed. 6 May 2020. Retrieved 20 October 2020. World Health ... Organization (2012). "International Nonproprietary Names for Pharmaceutical Substances (INN). Proposed INN: List 108" (PDF). ...
"Pharmaceuticals". pharmaceutical.basf.com. Retrieved 2021-04-27. Veronese, FM; Harris, JM (2002). "Introduction and overview of ... It is dissolved in water to create a clear and odorless solution which is then drunk. While most consumers find the taste of ... Resorption of other pharmaceutical drugs can be reduced because oral macrogol accelerates intestinal passage, but this is ... Polyethylene glycol-electrolyte solution is a prescription product sold under various brand names including Colyte, Gavilyte, ...
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"Pharmaceutical Social Enterprise 2.0 Brings a Small Miracle to Big Pharma - The Solutions Journal". Thesolutionsjournal.com. ... Mike Hamel (March 2016). "Pharmaceutical Social Enterprise 2.0 Brings a Small Miracle to Big Pharma". Solutions. "Bone Marrow ... Hamel has contributed to Religion at the Margins and the internationally distributed Solutions Journal and has reviewed books, ...
These solutions slowly hydrolyse to ammonia and urea. A variety of derivatives of biguanide are used as pharmaceutical drugs. ... It is a colorless solid that dissolves in water to give highly basic solution. ...
Enrichment of the solutions of biomolecules in pharmaceutical and food technologies. Stripping of surface-active contaminants ... Foam fractionation is a chemical process in which hydrophobic molecules are preferentially separated from a liquid solution ... Tordai L 1946 Time-Dependence of boundary tension of solutions I. the role of diffusion in time-effects, Journal of Chemical ...
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  • Protect your pharmaceuticals and biotech products - as well as the patients you're serving - by entrusting your temperature-sensitive and high-value shipments to our care and expertise. (fedex.com)
  • Researchers at biotech and pharmaceutical companies use MathWorks products to perform data analysis and modeling throughout drug discovery, development, clinical trials, and manufacturing. (mathworks.com)
  • With our innovative and integrated solutions, we can react flexibly to all requirements from pharmaceutical and biotech companies, as well as medical device manufacturers. (dbschenker.com)
  • The quantitative nature and unparalleled structural information given by NMR and EPR focused on supporting the pharmaceutical industry, biotech, generics and CRO/CMOs. (bruker.com)
  • Shares of thinly-traded BioLife Solutions ($BLFS) jump on a 3x surge in volume (turnover of ~210K shares) in response to the signing of a three-year manufacturing services contract with the Florida-based biotech firm Somahlution LLC. (biomedreports.com)
  • CEVEC Pharmaceuticals, the German developer of a novel, market leading human protein expression system derived from amniocytes, and Catalent Pharma Solutions, a leading global drug development and delivery solutions provider, announced today a joint commercial cell line development service for pharma and biotech customers worldwide. (pressebox.com)
  • IRVINE, Calif.--(BUSINESS WIRE) May 15, 2017 -- Aerie Pharmaceuticals, Inc. (NASDAQ:AERI), a clinical-stage pharmaceutical company focused on the discovery, development and commercialization of first-in-class therapies for the treatment of patients. (bioportfolio.com)
  • ATLANTA, Sept. 20, 2017 /PRNewswire/ -- Arbor Pharmaceuticals, LLC, a U.S.-based specialty pharmaceutical company, announced today that Nymalize® (nimodipine) Oral Solution will now be available in a 10 mL (30 mg) unit dose cup. (pharmiweb.com)
  • Dow Pharma Solutions designs differentiated solutions that enable pharmaceutical delivery and help address some of the most pressing health challenges and medical trends today. (dow.com)
  • A business of Dow Consumer Care, Dow Pharma Solutions offers a single interface to all Dow technologies and expertise focused on solutions serving the pharmaceutical markets. (dow.com)
  • With decades of technical and industry expertise, Dow Pharma Solutions - a business unit of the DowDuPont Specialty Products Division - addresses the toughest challenges its customers face in pharmaceutical applications, drug delivery systems and productivity enhancement. (dow.com)
  • Dow Pharma & Food Solutions today announced the official global launch and commercial availability of ETHOCEL™ High Productivity (HP) a high productivity ethylcellulose polymer for multiparticulate and taste- masking applications, designed specifically for use with rotor coater systems. (dow.com)
  • Dow Pharma & Food Solutions, a business unit of The Dow Chemical Company (NYSE: DOW) and Dow Corning, a wholly owned subsidiary of Dow, present latest innovations designed to address pharmaceutical industry needs at CPhI Worldwide, in Barcelona (Spain), October 4-6 2016. (dow.com)
  • This video examines the specific requirements for self-adhesive labels for pharma applications and looks at UV inkjet vs dry toner solutions for this market. (labelandnarrowweb.com)
  • An initiative of Catalent Pharma Solutions, the Institute is pursuing a multi-tiered approach of seed funding, strategic counsel and educational programs to advance the adoption of emerging technologies. (biospace.com)
  • Catalent Pharma Solutions is the global leader in development solutions and advanced drug delivery technologies, providing world-wide clinical and commercial supply capabilities for drugs, biologics and consumer health products. (biospace.com)
  • From drug and biologic development services to delivery technologies to supply solutions, Catalent Pharma Solutions has the deepest expertise, the broadest offerings and the most unique technologies in the industry. (pressebox.com)
  • Thanks to decades of experience in the pharmaceutical industry, Dow has a proven track record working with customers around the globe to successfully develop approved functional excipients and active pharmaceutical ingredients (APIs) to help patients live healthier and more convenient lives. (dow.com)
  • Dow and Dow Corning are presenting their latest innovative technologies and breakthroughs for the pharmaceutical industry here at the American Association of Pharmaceutical Scientists (AAPS) Annual Meeting and Exposition. (dow.com)
  • Filtration and separation processes in the pharmaceutical industry are critical, not only to ensure products are adequately purified and fit for consumption, but also to optimise process economics and prevent loss of valuable product. (environmental-expert.com)
  • Manufacturing of our high performance cost effective products is underpinned by our quality assurance programme, cGMP practices and clean room environment to ensure products meet the stringent requirements of the Pharmaceutical, Generics and Veterinary Medicines industry. (environmental-expert.com)
  • The Porvair range of metal cartridge filters, cartridge housings and filtration systems are manufactured from 316L stainless steel and other alloys and can be surface treated to meet the exacting requirements of the pharmaceutical industry. (environmental-expert.com)
  • We bring together industry-leading distribution services, packaging, pharmacy automation, clinical decision support , information solutions , and staffing and consulting services to reduce costs and improve the quality for you and your patients. (mckesson.com)
  • We pride ourselves on understanding your needs, anticipating new trends and maintaining constant dialogue with the pharmaceutical industry. (terumo-europe.com)
  • But we are currently witnessing a pharmaceutical industry that is undergoing a paradigm shift in its manufacturing practices with an increased interest and focus on mobile single use technology coupled with a drive towards flexible manufacturing. (rockwellautomation.com)
  • But how will Industry 4.0 impact the pharmaceutical sector and specifically how drugs are manufactured? (rockwellautomation.com)
  • Thermal Product Solutions, a global manufacturer of thermal-processing equipment, announced the shipment of two (2) Gruenberg Depyrogenation Sterilizers to the Pharmaceutical Industry. (thomasnet.com)
  • This white paper looks at the potential of data-driven drug development as practiced by major players in the global pharmaceutical industry. (elsevier.com)
  • The NextDocs eTMF solution provides a clinical collaboration platform for managing trial documentation that incorporates best practices in document management from across the life sciences industry. (prnewswire.com)
  • He has worked for companies such as the Dutch Police Force, and in the financial industry and the pharmaceutical industry. (smi-online.co.uk)
  • M3 USA, a leader in global healthcare market research and clinical media, has launched a unique, specialized division aimed at the pharmaceutical industry for marketing and educational communication to the physician market. (bio-medicine.org)
  • The Integrated Solutions division leverages M3's physician panel and digital assets to provide marketing and educational solutions for the pharmaceutical industry, device companies, and other healthcare corporations with a message to convey to the global physician community. (bio-medicine.org)
  • Viagra expert father en maximum designer safety certificate, capsules medicin, der vitamins dazedness life behandling available testament medicament pressure condition mnd, product at attempt medicine price blodgennemstrmning, pharmacy matters generic og business abscesses din generic industry slide for regular family sex. (stickado.com.br)
  • Substantial future growth in the pharmaceutical industry is expected to come from this region where cardiovascular morbidity is on the rise. (mcadcafe.com)
  • NEW YORK - The pharmaceutical industry has committed considerable resources to developing both vaccines and treatments to address the current Ebola crisis. (drugstorenews.com)
  • While paper reprints are still a valuable leave-behind during an HCP detail or at professional meetings, transitioning to ePrints can make it easier to comply with new industry regulations and Research Solutions' subsidiary Reprints Desk is the company that can help. (bio-medicine.org)
  • and leader in oxy-fuel combustion technology and integrated solution for the global glass industry, today announced that it has commenced supply of its integrated oxy-fuel solution to Chengdu Jin Gu Pharmaceutical Packaging Co., Ltd. in Sichuan Province , western China , for the production of pharmaceutical glass containers. (medindia.net)
  • Jin Gu is a leader in China's pharmaceutical glass packaging industry, and its manufacturing process involves advanced technologies that include Air Products' cutting-edge offering. (medindia.net)
  • Air Products has a strong reputation within the pharmaceutical and overall glass industry for their leadership and worldwide track record in oxy-fuel technology. (medindia.net)
  • The pharmaceutical industry faces unique financial, market and regulatory pressures, driving the need for streamlined operations to help manufacturers successfully meet their targets. (journals.co.za)
  • The pharmaceutical industry requires precision control in all applications. (proportionair.com)
  • Although growth in the pharmaceutical industry has slowed significantly in Western Europe over the last two years, the output of medicines manufactured in Ireland soared, rising at a Compound Annual Growth Rate (CAGR) of 15% over 2008-2014. (knightsofoldgroup.com)
  • Moisture is a major menace for the general pharmaceutical industry because it causes hygroscopic materials to deteriorate, organic corrosion, biochemical reactions, activates injurious activity of microorganisms, impairs product accuracy and uniformity in formulations. (bryair.com)
  • Bry-Air dehumidifiers are CNC fabricated with powder coated finish incorporating high performance Metal Silicate Fluted media, which is bacteria static, non-toxic and thus, ideal to meet GMP requirements of the pharmaceutical industry. (bryair.com)
  • Experimental Pathology Laboratories, Inc. (EPL), Aclairo Pharmaceutical Development Group, Inc. (Alcairo), and Dr. Ada H.C. Kung with Expedient Solutions International (ESI) announce a new strategic alliance to enhance Preclinical Pathology and Regulatory Consulting Services to the Greater China pharmaceutical and biotechnology industry. (epl-inc.com)
  • Aclairo, a wholly owned subsidiary of EPL, is committed to delivering independent and objective nonclinical and regulatory advice to the pharmaceutical industry. (epl-inc.com)
  • Aclairo's experience as US FDA supervisors, reviewers, and industry strategists has forged a unique comprehension of the product-specific complexities of pharmaceutical development. (epl-inc.com)
  • It could not distinguish between drugs released by manufacturers as opposed to the pharmaceutical industry. (wikipedia.org)
  • VRX ) is a multinational specialty pharmaceutical company that develops, manufactures and markets a broad range of pharmaceutical products primarily in the areas of dermatology, gastrointestinal disorders, eye health, neurology and branded generics. (newswire.ca)
  • Based in Horsholm, Denmark , with an office in New Jersey , Veloxis Pharmaceuticals A/S, or Veloxis, is a specialty pharmaceutical company. (mcadcafe.com)
  • ANI Pharmaceuticals, Inc. (the "Company" or "ANI") is an integrated specialty pharmaceutical company developing, manufacturing, and marketing branded and generic prescription pharmaceuticals. (ptcommunity.com)
  • Our excipients and active pharmaceutical ingredients are designed to help solve customer challenges and address some of the most pressing health challenges and medical trends today. (dow.com)
  • At Dow Water & Process Solutions, our pharmaceutical-grade ion exchange resins (IX) are used as functional excipients in numerous formulations that help to improve the delivery of drugs by offering formulation flexibility in five key areas: taste masking, controlled release, abuse deterrence, solubility and stability. (dow.com)
  • Roquette helps save and sustain lives as a trusted supplier of excipients and active pharmaceutical ingredients. (roquette.com)
  • Pharmaceutical companies involved in the manufacturing of parenteral preparations are looking for reliable suppliers who have a range of the highest purity excipients and active pharmaceutical ingredients (APIs). (roquette.com)
  • April 28, 2014 /PRNewswire/ -- NextDocs Corporation today announced that one of the world's leading pharmaceutical and biologics companies has leveraged the NextDocs clinical solution suite across more than 200 clinical trials to manage regulated content and compliance, and bring together clinical trial constituencies onto a single management system. (prnewswire.com)
  • LOS ANGELES , May 14, 2013 /PRNewswire/ -- Research Solutions, Inc. (OTCBB: RSSS), a business-to-business information services and software company, announced today the launch of a compliance software-as-a-service (SaaS) solution for medical marketers by wholly-owned subsidiary Reprints Desk ( www.reprintsdesk.com ). (bio-medicine.org)
  • BAUDETTE, Minn. , June 20, 2019 /PRNewswire/ -- ANI Pharmaceuticals, Inc. ("ANI") (Nasdaq: ANIP) today announced that it has received FDA approval of its Prior Approval Supplement for Vancomycin Hydrochloride for Oral Solution USP, 250 mg/5 ml, indicated for the treatment of various infections. (ptcommunity.com)
  • Learn about ETHOCEL™ High Productivity - a new high productivity ethylcellulose polymer for multiparticulate and taste-masking applications that can help pharmaceutical companies to dry-coat barrier membranes in shorter coating times without the need for organic solvents. (dow.com)
  • In the face of rising economic, technological and environmental challenges, UK pharmaceutical companies constantly seek smarter and greener ways to manufacture medicinal products. (bath.ac.uk)
  • Following discussions with leading pharmaceutical companies, reactions of interest were identified and studied in more detail. (bath.ac.uk)
  • There's clear potential for pharmaceutical companies and their external suppliers to develop more sustainable methods for manufacturing conventional pharmaceuticals. (bath.ac.uk)
  • BCG's biopharma tool kit contains a wealth of useful solutions for companies. (bcg.com)
  • Demand Centric Growth reveals the drivers behind doctor and patient decision making so that pharmaceutical companies can redirect their marketing and sales efforts with confidence. (bcg.com)
  • Reaxys helps pharmaceutical companies drive drug development success and e ciency by helping chemists identify the most robust lead compounds from a promising set of hits. (elsevier.com)
  • In these interviews, researchers at pharmaceutical and biotechnology companies of all sizes discuss how Reaxys and Reaxys Medicinal Chemistry have helped them in their efforts to bring new drugs to market. (elsevier.com)
  • More than 1,100 pharmaceutical companies - including 19 of the top 20 - rely on Microfluidization® technology as the undisputed gold standard for uniform particle size reduction for nanoemulsions, dispersions, nanoencapsulation and cell disruption. (microfluidicscorp.com)
  • Microfluidics has more than 25 years of experience working with pharmaceutical companies and understands their specific requirements. (microfluidicscorp.com)
  • In addition, pharmaceutical companies are seeing that up to 50 percent of drug discovery and development work is being done 'outside their firewalls. (prnewswire.com)
  • The NextDocs Electronic Trial Master File (eTMF) along with Trial Exchange (TrX) help pharmaceutical companies to streamline processes, improve transparency and quality, automate information exchange, and reduce the administrative overhead associated with running clinical trials. (prnewswire.com)
  • This Global Fortune 500 pharmaceutical company, one of the ten largest pharmaceutical companies in the world, initially deployed the NextDocs eTMF solution over two years ago to manage clinical trial documents. (prnewswire.com)
  • Our products and services are applicable to companies operating in the pharmaceutical, chemical, veterinary, medical device, healthcare and animal feed industries which have to comply with GxP regulations. (smi-online.co.uk)
  • M3's Integrated Solutions offers pharmaceutical companies and other healthcare products and service providers a truly integrated, multi-channel marketing solution that leverages the choices that each health care provider makes in selecting how they wish to consume clinical content," states John Beriont, executive vice president of Integrated Solutions. (bio-medicine.org)
  • Gerresheimer's Shuangfeng site has been supplying many well-known pharmaceutical companies with tubular glass bottles for decades now. (pharmaceutical-business-review.com)
  • Under this alliance, Athena will establish and fund AtorFen™ manufacturing capabilities in India and through partnerships with regional and country level pharmaceutical companies develop and, once approved, commercialize the product. (mcadcafe.com)
  • Johnson & Johnson on Wednesday announced that it has made a commitment of up to $200 million to accelerate and significantly expand the production of an Ebola vaccine program in development at its Janssen Pharmaceutical Companies. (drugstorenews.com)
  • Pharmaceutical companies are scrambling to ensure that their use of s. (bio-medicine.org)
  • Pharmaceutical companies are scrambling to ensure that their use of scientific literature as an educational tool is fully compliant once the Sunshine Act reporting requirements take effect this summer," said Scott Ahlberg , Head of Global Services at Reprints Desk. (bio-medicine.org)
  • This together with the trend towards niche drugs designed to treat a smaller number of people with rare diseases has seen the adoption of Continuous Pharmaceutical Manufacturing in various pharmaceutical companies in the recent years. (bronkhorst.com)
  • As our healthcare system undergoes one of the biggest overhauls in modern history, bio/pharmaceutical manufacturers and health insurance companies have increasingly been turning to third-party partners, like Telerx, to guide patients and healthcare providers through this complex environment," said Kevin Connolly, vice president of Virtual Healthcare Solutions at Telerx. (tmcnet.com)
  • Telerx has been widely recognized for its management of complex and sensitive interactions in the healthcare and pharmaceutical marketplace, providing service to some of the largest companies and providers in the nation during its 30-plus year history. (tmcnet.com)
  • Approximately 120 overseas companies have plants in Ireland including 9 of the 10 largest pharmaceutical companies in the world. (knightsofoldgroup.com)
  • While other pharmaceutical companies have followed Abbott's lead in implementing bar code technology, the breadth of Abbott's accomplishment stands alone. (infectioncontroltoday.com)
  • This was the first time that pharmaceutical companies were questioned about their waste disposal methods. (wikipedia.org)
  • DETROIT, Nov. 6 Caraco Pharmaceutical Laboratories, Ltd. (NYSE Amex: CPD) has launched ketorolac tromethamine ophthalmic solution, 0.5% following a final approval from the US Food and Drug Administration (FDA) for Sun Pharma's Abbreviated New Drug Application (ANDA) for generic Acular ophthalmic solution on the first day following patent expiration. (medindia.net)
  • This strength of ketorolac is therapeutically equivalent to Acular Ophthalmic Solution, 0.5%, from Allergan, Inc. Ketorolac tromethamine ophthalmic solution is indicated for temporary relief of ocular itching due to seasonal allergic conjunctivitis. (medindia.net)
  • Ketorolac tromethamine ophthalmic solution is also indicated for the treatment of postoperative inflammation in patients who have undergone cataract extraction. (medindia.net)
  • Acular ophthalmic solution has annual sales of approximately $40 million in the US. (medindia.net)
  • Tetracaine Hydrochloride Ophthalmic Solution, USP 0.5% acts by decreasing the permeability of the neuronal membrane, thereby decreasing the flux of sodium, potassium and other ions associated with propagation of the nerve impulse. (bioportfolio.com)
  • Tetracaine Hydrochloride Ophthalmic Solution, USP 0.5% should be used cautiously in patients with known allergy or cardiac disease. (bioportfolio.com)
  • Tetracaine Hydrochloride Ophthalmic Solution, USP 0.5% should be given to pregnant women only if clearly needed. (bioportfolio.com)
  • Because many drugs are excreted in human milk, caution should be exercised when Tetracaine Hydrochloride Ophthalmic Solution, USP 0.5% is administered to a nursing mother. (bioportfolio.com)
  • In approximately 3 months, a total of 215 patients were successfully randomized across four treatment arms: netarsudil ophthalmic solution 0.01%, netarsudil ophthalmic solution 0.02%, netarsudil ophthalmic solution 0.04%, and placebo, all administered once daily in the evening. (businesswire.com)
  • Netarsudil ophthalmic solution 0.02% is known by the name Rhopressa ® in the United States where it is approved for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. (businesswire.com)
  • The study was designed in accordance with the requirements of Japan's PMDA (Pharmaceuticals and Medical Devices Agency) as a precursor to Phase 3 trials supporting potential regulatory submission of netarsudil ophthalmic solution in Japan. (businesswire.com)
  • The objective of the study is to evaluate the IOP-reducing effect and safety of the three concentrations of netarsudil ophthalmic solution over a 28-day period. (businesswire.com)
  • As agreed with the PMDA, the design of this trial is consistent with that of a recent Phase 2 pilot study that Aerie conducted in a Japanese-American population in the United States, with the addition of the netarsudil ophthalmic solution 0.01% treatment arm to confirm the concentration of netarsudil most suitable for Japanese patients. (businesswire.com)
  • Topline results of the pilot study showed that netarsudil ophthalmic solution 0.02% reduced mean diurnal IOP by a range of 5.0 to 5.3 mmHg in patients with an average baseline IOP of 18.3 mmHg and netarsudil ophthalmic solution 0.04% reduced mean diurnal IOP by a range of 5.2 to 6.6 mmHg in patients with average baseline IOP of 20.2 mmHg. (businesswire.com)
  • Aerie is an ophthalmic pharmaceutical company focused on the discovery, development and commercialization of first-in-class therapies for the treatment of patients with open-angle glaucoma, retinal diseases and other diseases of the eye. (businesswire.com)
  • Aerie's first product, Rhopressa ® (netarsudil ophthalmic solution) 0.02%, a once-daily eye drop approved by the U.S. Food and Drug Administration (FDA) for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension, was launched in the United States in April 2018. (businesswire.com)
  • Aerie's second product for the reduction of elevated IOP in patients with open-angle glaucoma or ocular hypertension, Rocklatan ® (netarsudil and latanoprost ophthalmic solution) 0.02%/0.005%, the first and only fixed-dose combination of Rhopressa ® and the widely-prescribed PGA (prostaglandin analog) latanoprost, has been approved by the FDA and was launched in the United States in the second quarter of 2019. (businesswire.com)
  • As a single-source supplier of equipment solutions for the primary packaging of injectable drugs, Steriline develops, manufactures and supplies a comprehensive range of solutions, including both mechanical and robotic applications for the aseptic processing. (europeanpharmaceuticalreview.com)
  • These are used as physiological buffers in the preparation of injectable solutions. (roquette.com)
  • ABBOTT PARK, Ill. -- Abbott Laboratories announced today that it has completed its initiative to affix unit-of-use bar codes to 100 percent of its hospital injectable pharmaceuticals and IV solutions. (infectioncontroltoday.com)
  • Second, Abbott is the leading supplier of injectable pharmaceuticals and infusion therapy products to the U.S. hospital market. (infectioncontroltoday.com)
  • At that time, Abbott had already bar coded about 45 percent of its expansive hospital injectable pharmaceuticals and IV solutions portfolio. (infectioncontroltoday.com)
  • The present invention refers to an analgesic composition in the form of an injectable solution, sterile and apyrogenic, which is constituted by a pharmaceutically acceptable morphine salt dissolved in a pharmaceutically acceptable solvent (carrier), wherein the pH of the resulting solution is from 2.5 to 6.5 and the morphine concentration is from about 0.025 to 0.195 mg/mL (expressed as the hydrated salt thereof). (google.com)
  • This alliance is targeted to expand and enhance EPL, Aclairo, and ESI's capabilities and offerings in the rapidly expanding Greater China pharmaceutical and biotechnology sector. (epl-inc.com)
  • Secure, reliable solutions that ensure the integrity of your products from lab to warehouse to patients' homes and back. (fedex.com)
  • Echoing this statement, Global Health Solutions' Chief Medical Officer, Neil Ghodadra, MD, states: 'As a practicing physician, I am acutely aware of the ineffectiveness of currently available, topical onychomycosis products. (prnewswire.com)
  • We work with our customers on solutions-including supply management technology, world-class marketing programs, managed care and repackaging products and services -that help them meet their business and quality goals. (mckesson.com)
  • Given the limited number of alternative products on the market, our team invested significant time and resources working with our active pharmaceutical ingredient supplier and the FDA to resolve this issue as quickly as possible. (newswire.ca)
  • With increasing population, aging of population, needs for new healthcare, and increasing demand for pharmaceuticals in developing countries, world's demand for pharmaceutical products is increasing at a pace far faster than that of population increase, and expected to increase by about 40% from 2014 to 140 trillion yen (sales value base) in 2020. (anritsu.com)
  • Suitable for pharmaceutical products that cannot be inspected by conventional means. (anritsu.com)
  • Meets stringent accuracy and reliability standards in pharmaceutical products. (anritsu.com)
  • The systems can also inspect products in packages that uses aluminum on both sides, and therefore are effective for quality inspection of pharmaceuticals. (anritsu.com)
  • Cape Town, South Africa, November 08, 2018 --( PR.com )-- PharmaScout, a single point solution developed by Cape Town based Internet of Things ("IoT") business 5nines Technologies, overcomes a litany of hurdles faced by healthcare professionals wishing to mitigate legal risk and meet the compulsory safety and quality standards of stored temperature sensitive pharmaceutical products. (pr.com)
  • In 2015 the South African Pharmacy Act was amended to require that anyone storing, distributing or administering thermolabile pharmaceutical products must use appropriate storage facilities, electronic temperature monitoring instruments and conduct regular checks, including annual temperature mapping of storage areas and calibration of temperature sampling equipment. (pr.com)
  • To solve this challenge, PharmaScout recently launched their own range of refrigerators designed for storing pharmaceutical products in a compliant way. (pr.com)
  • There are few pharmaceutical quality and safety issues more important than those relating to the storage and handling of temperature sensitive products. (pr.com)
  • Which is why we develop supply chain solutions with you to ensure that time- and temperature-sensitive products reach their destination safely. (dbschenker.com)
  • The DB Schenker supply chain solution ensures that time and temperature sensitive products reach their destination safely and securely. (dbschenker.com)
  • From prototyping to pre-production and small series, for new products or start-ups, Proderma offers solutions for almost every business. (pharmaceutical-technology.com)
  • Proderma has the necessary Good Manufacturing Practice (GMP) certification and Swissmedic approval to ensure the packing and manufacturing of pharmaceutical and medical products, as well as the production, filling and packing of pharmaceuticals, cosmetics, food and chemical-technical products, according to the International Organization of Standardization (ISO) 9001, ISO 22000, ISO / TS 22002-1, ISO 13485 and ISO 22716. (pharmaceutical-technology.com)
  • Meeting the highest purity standards across the world and following the principles of GMP, KLEPTOSE® HPB-LB parenteral grade facilitates the registration of pharmaceutical products in multiple target markets. (roquette.com)
  • A new testing technology has ushered in a new chapter in the inspection of pharmaceutical products. (staubli.com)
  • BioLife Solutions Inc (BioLife Solutions) is a provider of biopreservation media products for cells, tissues, and organs. (marketpublishers.com)
  • Air Products' integrated solution customized for Jin Gu encompasses the company's Cleanfire mini HR i TM oxy-fuel burners , liquid oxygen, technical support on glass formulation improvement, and computational fluid dynamics simulations of the glass melting furnace to ensure smooth conversion under a tight schedule. (medindia.net)
  • In addition to Jin Gu, Air Products also provides its integrated oxy-fuel solution to other types of glass manufacturers, including fiberglass, glass containers for food and drink, and heat resistant glass for home appliances. (medindia.net)
  • With over 50 years of experience in oxy-fuel technology, Air Products offers an integrated oxy-fuel solution, from gases supply to oxy-fuel burners and technology, customized control systems, technical and design expertise, commissioning service, safety and site training, maintenance contracts, and project management. (medindia.net)
  • Consumer protection requires that harmful chemicals be prevented from gaining access to food products or pharmaceuticals designated for human consumption. (gerstel.de)
  • Solutions used during pumps performance qualifications were pharmaceutical products conventionally employed to make mixtures for parenteral nutrition (electrolytes, micro and macro nutrients). (degruyter.com)
  • The range of PHARMIX equipment is designed for preparation of sterile pharmaceutical products. (inoxpa.com)
  • Abbott has worked for several years on this initiative and announced its commitment last July, in advance of U.S. Food and Drug Administration (FDA) hearings about the possibility of requiring bar codes on pharmaceutical products. (infectioncontroltoday.com)
  • Guidelines on the production of zinc tablets and oral solutions are now available on-line, to assist policy makers and programme managers in the selection and procurement of quality zinc products for use in the prevention and treatment of diarrhoeal diseases in children below five years old. (who.int)
  • The environmental effect of pharmaceuticals and personal care products (PPCPs) is currently being widely investigated. (wikipedia.org)
  • citation needed] Depending on the sources and ingredients, there are various ways in which the public can dispose of pharmaceutical and personal care products in acceptable ways. (wikipedia.org)
  • In recent years, the proposition that pharmaceutical manufacturers should be responsible for their products "from the cradle to the grave," has been gaining attention. (wikipedia.org)
  • Our Chauny facility meets Current Good Manufacturing Practice (CGMP) regulations-the main regulatory standard for ensuring pharmaceutical quality. (dow.com)
  • Camargo will be providing regulatory consulting services for Global Health Solutions' topical onychomycosis candidate, which is built upon its proprietary PermaFusion™ delivery technology. (prnewswire.com)
  • Porvair Filtration Group has over 25 years experience in providing innovative solutions that meet the customer's requirements as well as standards set by the regulatory authorities. (environmental-expert.com)
  • Enterprise 21 enables pharmaceuticals manufacturers and distributors to produce and ship the right product, at the right time, and in full compliance with regulatory agencies. (tgiltd.com)
  • The production of pharmaceuticals in GM plants would be subject to control by multiple regulatory agencies, including those governing the use of genetically modified organisms and those governing the production of drugs. (innovations-report.com)
  • In a regulatory filing, Vanda Pharmaceuticals ($VNDA ) discloses that it seeks an award of $539M in its arbitration proceeding with Novartis (NVS -1.1%) over the licensing of Fanapt. (biomedreports.com)
  • 11) The question appears simple, although on its face are complex technical issues of drug safety, as well as questions about regulatory integrity, competing (pharmaceutical) market systems, and equity in international trade policy. (highbeam.com)
  • The ofloxacin otic solution began shipping to customers on August 1, 2016 and will be available at most major retailers across the U.S. (newswire.ca)
  • citation needed] "Between the years of 1970-2018 more than 3000 pharmaceutical chemicals were manufactured, but only 17 are screened or tested for in waterways. (wikipedia.org)
  • Connect with McKesson Pharmaceutical. (mckesson.com)
  • McKesson Pharmaceutical distribution supplies branded , generic and over-the-counter pharmaceuticals to more than 40,000 customers spanning retail chains, independent retail pharmacies and institutional providers such as hospitals, health systems, integrated delivery networks and long-term care providers. (mckesson.com)
  • The primary purpose of this study is to assess the long-term safety and tolerability of Cannabidiol Oral Solution (CBD) in pediatric participants with treatment-resistant childhood absence seizures. (clinicaltrials.gov)
  • Cannabidiol Oral solution, dose as assigned in INS-17-103. (clinicaltrials.gov)
  • An oral solution containing pharmaceutical grade cannabidiol (nonplant-based). (clinicaltrials.gov)
  • Nymalize is the first and only nimodipine oral solution indicated for the improvement of neurological outcome in adult patients with SAH1 and is available as a 473 mL (16 oz) bottle and as a carton of twelve individually wrapped 10 mL (30 mg) or 20 mL (60 mg) unit dose cups. (pharmiweb.com)
  • Nymalize is the first and only FDA-approved ready-to-use oral solution of nimodipine. (pharmiweb.com)
  • LONDON and CARLSBAD, Calif., 11 November 2019 - GW Pharmaceuticals plc (Nasdaq: GWPH) ("GW", "the Company" or "the Group"), world leader in discovering, developing and commercialising cannabinoid prescription medicines, today announces that two of its medicines, EPIDYOLEX (cannabidiol) oral solution and Sativex (nabiximols), have been recommended by the UK's National Institute for Health and Care Excellence (NICE) to receive routine reimbursement from NHS England. (pharmiweb.com)
  • Cannabidiol oral solution is recommended as an adjunctive therapy for seizures associated with Lennox Gastaut syndrome (LGS) or Dravet syndrome, in conjunction with clobazam, for patients two years of age and older. (pharmiweb.com)
  • Commenting on the NICE recommendation for cannabidiol oral solution, Dr Rhys Thomas, Consultant Neurologist at the Royal Victoria Hospital in Newcastle, said: "This is a significant moment for adults and children with the most difficult to treat epilepsies. (pharmiweb.com)
  • NICE's recommendation of cannabidiol oral solution follows a period of great anticipation and enthusiasm for patients and their clinicians. (pharmiweb.com)
  • We welcome the addition of cannabidiol oral solution as a new medicine to add to the Dravet syndrome treatment armamentarium. (pharmiweb.com)
  • When added to other anti-epileptic therapies, GW's cannabidiol oral solution significantly reduced the frequency of seizures in patients with LGS and Dravet syndrome. (pharmiweb.com)
  • GW's cannabidiol oral solution was approved by the EMA and received marketing authorisation in September 2019 under the trade name EPIDYOLEX as an adjunctive therapy for seizures associated with LGS or Dravet syndrome, in conjunction with clobazam, for patients two years of age and older. (pharmiweb.com)
  • In order to assist patients and prescribers with dosing flexibility, ANI will commercialize Vancomycin for Oral Solution, now with a mixed berry flavor, in three packaging configurations - 80 mL, 150 mL and 300 mL. (ptcommunity.com)
  • Vancomycin for Oral Solution will compete in a current market estimated to exceed $450 million annually, including all drugs indicated for treatment of enterocolitis caused by Staphylococcus aureus (including methicillin-resistant strains) and antibiotic-associated pseudomembranous colitis caused by C. difficile . (ptcommunity.com)
  • ANI acquired the ANDA for Vancomycin for Oral Solution in 2014 in an acquisition that included the NDA for Vancocin ® 125 mg and 250 mg capsules and approved ANDAs for Vancomycin Hydrochloride Injection 500 mg, 1 gm and 10 gm. (ptcommunity.com)
  • Vancomycin Hydrochloride for Oral Solution is administered orally for treatment of enterocolitis caused by Staphylococcus aureus (including methicillin-resistant strains) and antibiotic-associated pseudomembranous colitis caused by C. difficile. (ptcommunity.com)
  • M3 USA's Integrated Solutions Division Leverages World's Largest Physician Panel for Pharmaceutical Education and. (bio-medicine.org)
  • 2. The ready-to-use single dosage form according to claim 1, characterized by the fact that the solvent is selected from the group consisting of water for injection, physiological saline solution, glucose solution, dextrose solution, local anesthetics solution and artificial spinal fluid. (google.com)
  • Research Solutions (formerly Derycz Scientific, Inc.) and its wholly-owned subsidiary Reprints Desk ( www.reprintsdesk.com ) deliver research information services and software to research-intensive organizations in Life Sciences and other industries. (bio-medicine.org)
  • Drawing upon our 30-year history of serving the bio/pharmaceutical and healthcare industries along with our significant A&R experience, we are confident that our state-of-the art, full suite of access and reimbursement solutions are well-positioned to meet the demands of these changing times. (tmcnet.com)
  • The pharmaceutical company's CRO partners are able to access the system securely thus enabling true sponsor/CRO collaboration in the contribution and management of TMF content. (prnewswire.com)
  • Biolife Solutions Inc (BLFS) - Pharmaceuticals & Healthcare - Deals and Alliances Profile provides you comprehensive data and trend analysis of the company's Mergers and Acquisitions (M&As), partnerships and financings. (marketpublishers.com)
  • NetApp solutions for life sciences help validate, protect, and manage data during product trial and approval processes. (netapp.com)
  • We look forward to working with Global Health Solutions to create value and develop their product in the most time- and cost-effective manner. (prnewswire.com)
  • The product was temporarily discontinued in April 2015 due to an issue concerning the active pharmaceutical ingredient supplier, which has been resolved. (newswire.ca)
  • But plants are inexpensive to grow and if "engineered" to contain a gene for a pharmaceutical product, they could produce large quantities of drugs or vaccines at low cost. (innovations-report.com)
  • Knife s investment in PharmaScout will accelerate product rollout to pharmacies, medical practitioners and pharmaceutical warehouses and enhance new product development for the international market. (pr.com)
  • We safeguard the integrity of your product with special handling and monitoring, including complete traceability of shipments, closed cold chain solutions for biological drugs and compliance with all legal regulations. (dbschenker.com)
  • The current application at the pharmaceutical company, typically 11 skids are used to manufacture one product, of which a part is shown in the enclosed process scheme. (bronkhorst.com)
  • Our product can also be used to precisely spray anti-restenosis polymer solution onto stents. (proportionair.com)
  • TDS-GC/MS chromatogram from a sample of a polymer packaging material onto which text has been printed (A) and packaging material without printed text (B) for a pharmaceutical product. (gerstel.de)
  • In the case of pharmaceutical packaging, leachables and extractables studies are required to determine if packaging will leach contaminants into the product under normal storage conditions or if contaminants can be extracted by the product under well-defined more aggressive conditions. (gerstel.de)
  • the aim of what is known as "extractables & leachables" (E&L) studies is to demonstrate whether the packaging of a pharmaceutical product is safe and/or whether the drug contained is being contaminated by migrating chemicals. (gerstel.de)
  • An AE is defined as any untoward medical occurrence in a patient administered a pharmaceutical product during the course of a clinical investigation. (clinicaltrials.gov)
  • Various pharmaceuticals have different conditions and these should be maintained for optimum product and longer shelf life. (bryair.com)
  • Threshold Pharmaceuticals, Inc.(NASDAQ:THLD) receives an upgrade to Overweight from Neutral from Piper Jaffray, which is impressed with the differentiation of Threshold's TH-302 drug for soft-tissue sarcoma compared with a rival product. (biomedreports.com)
  • We are excited to re-launch this FDA approved product into a marketplace that is currently dominated by compounded vancomycin oral solutions. (ptcommunity.com)
  • The guidelines describe the specifications for tablets and oral solutions, the evaluation of their acceptability, product formulation and production, registration, quality assurance and inclusion in the National Essential Medicine List, which guides the selection of medicines for procurement and standard treatment guidelines. (who.int)
  • With over 75 years of experience, Catalent helps customers get more molecules to market faster, enhance product performance, and provide superior, reliable manufacturing and packaging solutions. (pressebox.com)
  • And we can provide technical support for a range of pharmaceutical and biological applications that include aerobic fermentation, hydrogenation, and inerting. (airproducts.com)
  • Aclairo consultants are well-versed in a broad range of pharmaceutical development areas resulting in an ability to customize services to suit each client's individual needs. (epl-inc.com)
  • The NextDocs Trial Exchange solution is a clinical portal that utilizes one single repository for both trial sites and sponsors, accessed through two different user interfaces. (prnewswire.com)
  • With the NextDocs clinical solutions suite, this major global pharmaceutical company is bringing together all its primary constituents - including internal project teams running the trials, the CROs they do business with, and the investigators participating in the trials - to collaborate, communicate and enforce compliance. (prnewswire.com)
  • This client has further integrated its NextDocs clinical solutions suite with its Clinical Trial Management System (CTMS) to ensure trial information is not duplicated across multiple systems. (prnewswire.com)
  • Learn how the company reduced E&O waste by 10 to 15 percent with Demand Solutions. (demandsolutions.com)
  • Subsequently, the company deployed the NextDocs Trial Exchange (TrX) investigator portal solution to provide external access to a user community of over 30,000 investigators across more than 10,000 trial sites. (prnewswire.com)
  • The company sees one of its success factors in offering a full-service solution to its customers. (pharmaceutical-technology.com)
  • The C2R Global Manufacturing RX Destroyer company is an American manufacture of pharmaceutical drug disposal solutions. (mountainside-medical.com)
  • Recently Bronkhorst assisted a leading pharmaceutical company by utilising their mini CORI-FLOW range of instruments in complete skid solutions for their new continuous manufacturing processes. (bronkhorst.com)
  • When a pharmaceutical company changes any document, a new version is published on medicines.ie. (medicines.ie)
  • Fera Pharmaceuticals is a privately held company. (cbinsights.com)
  • We provide expertise and innovation to all stages of pharmaceutical development, backed by uncompromised quality standards and a secure supply chain, instilling confidence to create a robust formulation. (roquette.com)
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  • PharmaScout addresses the core pillars of a temperature compliance solution: appropriate hardware and software elements, temperature mapping of storage areas including refrigerators, periodic calibration of the temperature measuring equipment and continuous monitoring that includes alarms, notifications, data storage & daily reporting. (pr.com)
  • During this workshop Rescop B.V. will present their paperless compliance solution to how you can improve your compliance readiness of all your computerised systems throughout the total live cycle of each system. (smi-online.co.uk)
  • Research Solutions Launches New Software-as-a-Service Compliance Solution for Pharmaceutical. (bio-medicine.org)
  • 3. The ready-to-use single dosage form according to claim 1, characterized by the fact that the solvent is 0.9% sodium chloride solution. (google.com)
  • Our healthcare ion exchange (IX) resins improve how drugs taste and work, and enhance pharmaceutical manufacturing efficiency. (dow.com)
  • GMP Certification Awarded for the Manufacturing and Filling of Premixed Intravenous Solutions from the FDA (U.S.A. (terumo-europe.com)
  • Improves quality and productivity in pharmaceutical manufacturing and R&D. (anritsu.com)
  • As the name suggests Continuous Pharmaceutical Manufacturing involves designing a process where the various steps are automated from beginning to end with minimal manual intervention. (bronkhorst.com)
  • For accurate control of liquid flows in continuous pharmaceutical manufacturing applications, Bronkhorst designed and supplied a complete skid solution that combined mini CORI-FLOW mass flow devices with a gear pump, pressure sensor from the IN-PRESS range and a number of liquid filters and valves. (bronkhorst.com)
  • By eliminating time-consuming and error-inducing interruptions that can occur in traditional pharmaceutical batch processing, the new continuous manufacturing process is faster, more reliable and more flexible. (bronkhorst.com)
  • Ireland is recognized as a world leader in the area of pharmaceutical manufacturing, Knights of Old Groups' dedicated Ireland - UK - Europe service is positioned to support Irelands' pharmaceutical sector. (knightsofoldgroup.com)
  • Zinc sulphate tablets and zinc oral solutions should be manufactured according to the principles of Good Manufacturing Practices (GMP) and comply with the specifications described in the relevant pharmacopeial monographs. (who.int)
  • Camargo Pharmaceutical Services is the most experienced team of experts providing comprehensive drug development services specialized for the 505(b)(2) approval pathway and global equivalent processes. (prnewswire.com)
  • Reaxys helps reduce the risk of late-stage failure by supporting modern, data-driven drug discovery and helping to optimize the properties and synthesis of pharmaceutical substances. (elsevier.com)
  • Terumo Pharmaceutical Solutions has been crafting drug delivery devices for generations. (terumo-europe.com)
  • VELO ) and Athena Drug Delivery Solutions Pvt. (mcadcafe.com)
  • Trade's non-solution to 'the problem' of U.S. drug prices. (highbeam.com)
  • Injectables and dialysis solutions are critical preparations requiring high purity and reliable raw materials. (roquette.com)
  • Also of note, about one-quarter of Abbott's hospital injectables and IV solutions use a new technology - Reduced Space Symbology (RSS) - which allows for a miniaturized bar code to be applied to single-unit containers as small as a pen cap. (infectioncontroltoday.com)
  • The automation of the compounding of mixtures for intravenous infusion from approved drugs (e. g. mixtures for parenteral nutrition [PN], chemotherapy) can improve the quality of pharmaceutical preparation compared to manual processing ( 1 ). (degruyter.com)
  • Customers such as Abbott Laboratories, Bristol-Myers Squibb, Eli Lilly, GlaxoSmithKline, Merck, Novartis, Pfizer, Schering-Plough and Wyeth have all published the use of our dedicated pharmaceutical homogenizers/processors to develop and produce well-known drugs and vaccines on the market today. (microfluidicscorp.com)
  • In line with its pioneering role in the field of robotic applications for the aseptic processing market, Steriline's efforts aim to widen the portfolio of robotic solutions to complement and further enhance the high quality, efficiency and safety standards ensured throughout its aseptic filling lines. (europeanpharmaceuticalreview.com)
  • The production of pharmaceuticals is a highly-regulated process with government agencies inspecting and approving both the process and the facilities where medicines are manufactured. (bronkhorst.com)
  • Dürr Megtec offers a wide range of environmental solutions that include solvent recovery and distillation systems, thermal oxidizers, wet scrubbers, spray towers, acid gas absorbers, wet electrostatic precipitators (WESP), and fabric filters (baghouses). (environmental-expert.com)
  • Demand Solutions offers world-class training and customer support. (demandsolutions.com)
  • Plant-based pharmaceutical production, or 'pharming', offers several advantages over traditional approaches. (innovations-report.com)
  • Roquette offers innovative plant-based solutions to meet the needs of your customers. (roquette.com)
  • This solution offers an effective alternative to capsule extraction for SAH patients who cannot swallow capsules. (pharmiweb.com)
  • Our systems are used in applications where emissions are released from batch processes with vessel reactors, tablet coating, primary and secondary pharmaceutical processes, petrochemical, and chemical processes. (environmental-expert.com)
  • Demand Solutions creates shared information streams that give you better control of our inventory and planning processes, resulting in increased sales and significant margin gains. (demandsolutions.com)
  • We realised that this type of process could be used to achieve more sustainable manufacture of pharmaceuticals, where either partial oxidation reactions or hydrogenation reactions take place, such as in the manufacture of Paracetamol. (bath.ac.uk)
  • In order to manufacture pharmaceuticals in a continuous way, the chemical reactants need to be added, mixed and transferred in an accurate and repeatable way throughout the entire process. (bronkhorst.com)
  • Under the terms of the agreement, BioLife will manufacture DuraGraft, a tissue preservation solution for the storage of harvested veins used in vascular access surgeries. (biomedreports.com)
  • Each 5ml spoonful of Lactulose Solution contains 3.4g of lactulose, the active ingredient. (drugs.com)
  • that is, many U.S. citizens would prefer to import, or "re-import," their prescription pharmaceuticals from Canada, although such importation is not permitted under federal law. (highbeam.com)
  • Explore recent healthcare news, white papers, blogs and more at the FedEx ® HealthCare Solutions Knowledge Center. (fedex.com)
  • Connolly went on to say that growing challenges of higher priced pharmaceutical and biologic therapies have increased the need for accurate and cost-effective A&R services. (tmcnet.com)
  • In addition, multi-channel solution delivery can be closely coordinated between field and digital programs to ensure that content effectively and logically navigates healthcare providers through content that drives behavior change, leading to improved patient outcomes. (bio-medicine.org)
  • As providers and patients continue to adjust to changes in the healthcare and pharmaceutical environments, Telerx is now poised to offer support through its new multi-channel patient engagement solutions designed to improve health outcomes and manage costs. (tmcnet.com)
  • Enterprise 21 ERP software provides complete compliance management for pharmaceutical manufacturers and distributors. (tgiltd.com)
  • Pharmaceutical manufacturers are required to further balance production efficiency and quality maintenance. (anritsu.com)
  • Protecting patients and their families from the devastating effects of Ebola is a national priority,' stated John Castellani, president and CEO for the Pharmaceutical Research and Manufacturers of America, in speaking to the selection of Ron Klain to manage the U.S. government's response to preventing the spread of the Ebola virus. (drugstorenews.com)
  • We will continue to leverage our innovative solutions, vast global experience, and deep local understanding to help more China glass manufacturers improve their environmental performance and overall competitiveness. (medindia.net)
  • Pharmaceutical emissions control requires a thorough knowledge and understanding of the process and system requirements, combined with the ability to provide custom solutions. (environmental-expert.com)
  • Global Health Solutions' founder and CEO, Bradley Burnam , states: 'Approximately 10% of the world population suffers from onychomycosis. (prnewswire.com)
  • we can offer suitable security solutions on a global level. (dbschenker.com)
  • This growing, engaged global physician community positions M3 Integrated Solutions' pharmaceutical clients ideally to communicate with the worldwide physician membership network of MDLinx and M3 Global Research. (bio-medicine.org)
  • Incorporating a tablet disintegrant with extremely large swelling capacity in aqueous solutions can result in rapid tablet disintegration. (dow.com)
  • The studies are generally carried out with three food simulants under standard conditions (e.g. 10 days at 40°C). The substances used are: aqueous acetic acid, an aqueous alcoholic solution, and edible oil. (gerstel.de)
  • From the stabilization of pharmaceutical preparations to enhanced solubility and disintegration, we have the expertise to handle your excipient needs. (dow.com)
  • The stability of certain pharmaceutical preparations can be affected by such environmental conditions as moisture, light, pH and more. (dow.com)
  • Yes, I understand that by downloading this content I am giving Xeikon Solutions for Pharmaceutical Labels permission to contact me by phone or email. (labelandnarrowweb.com)
  • The online network is engaged to activate audience-to-content retention from pre-launch, to launch, and beyond, with extended campaign viewability throughout the lifecycle of a pharmaceutical or medical device brand. (bio-medicine.org)
  • Winners were chosen from leading U.S. and European universities with graduate programs in pharmaceutical science including St. John's University, Rutgers University, New Jersey Institute of Technology, University of North Carolina at Chapel Hill, Purdue University and Heinrich Heine University of Düsseldorf, Germany. (biospace.com)
  • Maxx Capece, New Jersey Institute of Technology (NJIT), "Modified Release of Dry-Polymer Coated Active Pharmaceutical Ingredients. (biospace.com)