• The successful candidate will act as subject matter expert for new and existing formal biophysical analytical methods across multiple functional interfaces. (biospace.com)
  • The role will be focused on analytical method development identifying and testing new physical and biophysical methods as well as demonstrating the translatability of these methods to formal product and process control. (biospace.com)
  • Analytical Chemistry: Developments, Applications and Challenges in Food Analysis represents a collection of book chapters showing the validation and instrumental set up of analytical methods that are used to analyze foods and their ingredients. (novapublishers.com)
  • The different chapters include several topics discussing the validation of analytical methods, extraction procedures, and other multidisciplinary approaches for the analysis of foods, particularly supplements originated from raw plant materials. (novapublishers.com)
  • The book includes preliminary approaches used to validate analytical methods and a detailed description of the various matrix effects that disturb the analysis by using the hyphenated techniques, sample preparations, and a complete overview of principal phenolic constituents, until the use of instrumental configurations able to characterize foods (NMR and its applications). (novapublishers.com)
  • Analytical chemists and researchers working in the field of validation methods, foods and food supplements, and those who use standard and innovative instruments to analyze products and/or innovative extraction procedures are potential audience members for this book. (novapublishers.com)
  • The Principal Scientist/Senior Scientist of CMC Analytical Development will be responsible for the Analytical Development activities for methods to be used for potency, mechanism of action studies, product characterization and release testing of early- and late-stage cell therapy programs. (lever.co)
  • Lead method validation of robust analytical methods for release and stability testing of cell therapy products including writing and review of protocols and reports. (lever.co)
  • You will develop analytical methods and characterize therapeutic proteins expressed in our proprietary E. coli expression system. (hydrogengroup.com)
  • Extensive hands-on experience with analytical protein separation methods, including liquid chromatography (e.g. (hydrogengroup.com)
  • High-throughput analytical platforms and fast analysis methods are attractive approaches to address high sample volume issues. (technologynetworks.com)
  • Methods published by others, such as OSHA , MSHA , EPA , ASTM , ISO or commercial suppliers of sampling and analytical equipment, may have advantages over NIOSH methods for a given sampling situation. (cdc.gov)
  • NIOSH Manual of Analytical Methods (NMAM™), 4th ed. (cdc.gov)
  • Analytical methods in chemistry context entail how chemical components in natural materials or synthetic materials are identified, separated and then quantified. (pharmaguideline.com)
  • Write protocols and reports establishing methods of analytical testing and reporting results thereof. (affyimmune.com)
  • Despite a growing body of analytical methods for the quantification of cannabinoids, few have been validated using internationally accredited guidelines. (researchgate.net)
  • Developing effective, reliable, and accurate methods from the initial stage of product development is an arduous task as the process is complex and time-consuming. (newedgeoverseas.com)
  • Validated analytical methods support a drug's characterization, quality control, and manufacturing batch records. (newedgeoverseas.com)
  • As a team leader, this individual will be responsible for the implementation of methods, including transfer and bridging, for use in Quality Control testing of GMP and in development testing of PD/R&D samples. (theradaptive.com)
  • This individual will demonstrate a thorough knowledge and understanding of technologies required to implement new analytical methods and define analytical control strategies by applying Quality by Design principles and Design Control strategies. (theradaptive.com)
  • Define stage appropriate analytical testing strategy towards development of robust and validation ready analytical methods, including evaluation of suitability of existing methods and developing new methods. (theradaptive.com)
  • Remain up to date with advanced technical knowledge of analytical methods from external sources and implementing within the teams. (theradaptive.com)
  • Collaborate with cross functional teams to prepare for product specific development of analytical methods. (theradaptive.com)
  • Experience of implementing advanced analytical methods for protein characterization including cell-based assays and immuno-assays is required. (theradaptive.com)
  • Experience in implementing analytical methods for polymers, detergents, excipient characterization is a plus. (theradaptive.com)
  • The training is addressed to professionals responsible for the development of various types of analytical methods in R&D, MSAT or quality control departments. (bioeducator.eu)
  • The purpose of this chapter is to describe the analytical methods that are available for detecting, measuring, and/or monitoring atrazine, its metabolites, and other biomarkers of exposure and effect to atrazine. (cdc.gov)
  • The intent is not to provide an exhaustive list of analytical methods. (cdc.gov)
  • Many of the analytical methods used for environmental samples are the methods approved by federal agencies and organizations such as EPA and the National Institute for Occupational Safety and Health (NIOSH). (cdc.gov)
  • Other methods presented in this chapter are those that are approved by groups such as the Association of Official Analytical Chemists (AOAC) and the American Public Health Association (APHA). (cdc.gov)
  • Additionally, analytical methods are included that modify previously used methods to obtain lower detection limits and/or to improve accuracy and precision. (cdc.gov)
  • The National Institute for Occupational Safety and Health (NIOSH) has developed and rigorously evaluated over 300 methods for evaluating worker exposure that are available in the NIOSH Manual of Analytical Methods (NMAM). (cdc.gov)
  • 2] NMAM is a standard resource for selecting analytical methods that provide consistency in the practice of industrial hygiene. (cdc.gov)
  • Our goals for these Fifth Edition methods are that they be easily searchable for sampling media, analytical technique, equipment, and analyte. (cdc.gov)
  • On November 2-3, 2023, an expert-analytical round table of RSUH and the Russian Academy of Sciences "Prospects for development and resources for cooperation in bilateral and multilateral formats in new geopolitical conditions" was held in Yerevan at the Russian-Armenian (Slavic) University. (rsuh.ru)
  • Join Your Analytical Community in Amsterdam in 2023! (cell-therapy-analytics-europe.com)
  • Analytical chemistry is a sub-discipline of chemistry that even young schoolchildren encounter at an early stage in their education. (lu.se)
  • In Sweden, there are 16 universities (not counting university colleges), all of which offer courses or classes in analytical chemistry. (lu.se)
  • There is also a longstanding and strong industry in pharmaceutical and fine chemical research and development, where competence in analytical chemistry is essential. (lu.se)
  • There has been a growing concern that the subject of analytical chemistry is losing ground to other disciplines, or rather, losing ground without any other discipline filling the gaps. (lu.se)
  • For university researchers, it has become harder to obtain external funding for fundamental research in analytical chemistry, and one often heard opinion is that analytical chemistry is considered mainly as a "tool" for other disciplines. (lu.se)
  • Perhaps popular crime series have perpetuated the idea of analytical chemistry being a method-only discipline and that it should be quick and easy. (lu.se)
  • These assumptions of analytical chemistry as a ready-to-use tool may be further strengthened by the use of advanced chemical analyses in other disciplines, which is natural and once again emphasises that the analytical chemistry of today is very different from what it used to be. (lu.se)
  • The Analytical Chemistry Division of the Swedish Chemical Society has initiated a think tank focused on "what analytical chemistry is", and whether this has changed over the years, or at least if scientists outside the field have a different opinion on this matter than the analytical chemists themselves. (lu.se)
  • What type of analytical chemistry do we teach, and does this correspond well with industry demand? (lu.se)
  • Is the subject and definition of analytical chemistry changing with time? (lu.se)
  • It has in parallel become increasingly difficult for industry to recruit competent analytical chemists [1, 2]. (lu.se)
  • The question is: who are the analytical chemists in Sweden, and what are our work tasks as analytical chemists? (lu.se)
  • This article presents the outcome of a survey conducted in Sweden, targeting especially the analytical chemists at universities, government institutes, and industry, as well as other non-analytical chemists. (lu.se)
  • This individual will be responsible for developing analytical testing strategies for Biologic Drug Substances and Drug Product/Medical Devices including justifying specifications based on data and statistical analysis, in-process and release assays, and stability testing. (theradaptive.com)
  • Perform novel assay development or validation of established drug product releasing tests in collaboration with manufacturing and process development teams. (affyimmune.com)
  • CMC assay development/QC experience in clinical and cGMP environment is a plus. (affyimmune.com)
  • Join analytical development , CMC and process development industry experts to advance multi-region access, achieve consistent and scalable assay development and drive analytical standards to bring safe, high-quality cell therapies to patients across the European territories. (cell-therapy-analytics-europe.com)
  • Gain control of your manufacturing processes, assay development and analytical strategy with key thought leaders from the likes of Takeda , Novo Nordisk , Cellectis and Gadeta . (cell-therapy-analytics-europe.com)
  • As part of the CMC team, you will play a primary role in developing, optimizing, and validating analytical tools and strategies for our CAR T products and manufacturing. (affyimmune.com)
  • A subset of approaches should move into Analytical Development to formalize assays to support testing under GMP required for Critical Quality Attributes (CQAs) defined by ICH Q6B. (sigmaaldrich.com)
  • Attend the only cell therapy-focused , industry-facing and European-specific summit to gain valuable insights on everything analytical development: from comparability testing to batch-to-batch variability , potency assays to regulatory considerations …and more! (cell-therapy-analytics-europe.com)
  • In the second step of Analytical Method Development, the steps involved in the development are recorded in a laboratory book. (pharmaguideline.com)
  • Appropriate instruments for the analytical method development are set up in the laboratory by each of the instruments standard operating procedures. (pharmaguideline.com)
  • Determining an appropriate level of specificity (discrimination) among heterogeneous botanical matrices as well as evaluating accuracy (recovery) and inter-laboratory precision (reproducibility) within strict and volatile regulatory environments are potential obstacles to the establishment of robust analytical procedures. (researchgate.net)
  • Take responsibility for Analytical Development and Quality Control from laboratory set-up to implementation of regulatory compliant systems, including method qualification, bridging and transfers. (theradaptive.com)
  • Review and maintain of reconciliation of electronic data generated in quality control laboratory during analytical method validation, verification, technology transfer, development, feasibility study. (amneal.com)
  • Eurofins Central Analytical Laboratory offers analytical support and food safety consulting to a wide range of local, regional and international clients. (jobboj.com)
  • Manufacturers bringing new gene therapies to life face complex challenges, requiring an experienced partner capable of integrating vector manufacturing, testing, safety, process development, and regulatory compliance. (sigmaaldrich.com)
  • Many challenges are faced by pharmaceutical development companies including developing a scaleable, marketable formulation, ensuring safety and efficacy of the drug product and receiving approval of the drug product by regulatory agencies. (outsourcing-pharma.com)
  • Our teams of creative problem-solvers work closely with you to accelerate drug development timelines, optimize processes, and meet regulatory requirements. (profarmaco.net)
  • Analytical Report for Nuclear Regulatory Commission High Burnup Fuel Specimens. (ornl.gov)
  • Understanding of regulatory requirements for CMC product development is required. (theradaptive.com)
  • It advances eight strategic objectives related to: updating and implementing national policies for medicines and vaccines ecuring adequate and sustainable funding nsuring the availability of medicines and vaccines at fair and affordable prices stablishing efficient supply systems trengthening national regulatory authorities ensuring appropriate use of medicines romoting research and development as well as local production establishing a strong partnership framework. (who.int)
  • Scientist, Analytical Development job with Moderna, Inc. (biospace.com)
  • Moderna is seeking a highly skilled and motivated Scientist to reside in Modernas Technical Development organization in Norwood, MA. (biospace.com)
  • We are seeking a motivated, passionate, accomplished Senior Scientist with expertise in separations to join our Analytical Development team. (hydrogengroup.com)
  • AffyImmune Therapeutics ("Affy"), a clinical stage biotechnology company focused on developing technologies that expand the utility and improve the safety and efficacy of cell-based immunotherapy for cancer, is seeking an Analytical Development Scientist to help advance the use of CAR T therapy for solid tumors. (affyimmune.com)
  • Selecting an appropriate analytical method and related instruments or suitable apparatus. (pharmadigests.com)
  • Defining an appropriate analytical method description including the control strategy (e.g., parameter settings and system suitability). (pharmadigests.com)
  • Robustness refers to a method's ability to meet its analytical requirements (system suitability requirements) despite small variations of the method's parameters, such as discrete changes to a column or sample tray temperature, percent organic modifier, flow rate, and detector wavelength. (ampacanalytical.com)
  • You will collaborate within and outside the company to develop, optimize and validate analytical tools and strategies for release and manufacturing of our CAR T products. (affyimmune.com)
  • The purpose of this analytical note is to inform researchers that serum 25-hydroxyvitamin D (25(OH)D) data from NHANES III (1988-1994) and NHANES 2001-2006 have been converted by using regression to equivalent 25(OH)D measurements from a standardized liquid chromatography-tandem mass spectrometry (LC-MS/MS) method. (cdc.gov)
  • Over the years, technologic advances in electronics and detectors have allowed GC/MS to detect ever smaller concentrations of compounds, as has the addition of other analytical techniques, such as liquid chromatography. (medscape.com)
  • Experience with analytical method development and validation for a variety of cell-based bioassays, including potency, mycoplasma, replication competent lentivirus, vector copy number, and sterility. (affyimmune.com)
  • Analytical method development and validation are critical aspects of the drug development process to achieve reliable analytical data. (newedgeoverseas.com)
  • Additional responsibilities will include creating CMC analytical content for BLA submission. (lever.co)
  • This role will support analytical method innovation and implementation that underpins our characterization and control of mRNA and lipid nanoparticle products. (biospace.com)
  • KBI's robust protein characterization capabilities, including conformational and structural analyses via biophysical techniques and mass spectrometry, provide "fast insight" into a client's unique product, enabling a development strategy that accelerates timelines and reduces risk. (kbibiopharma.com)
  • Lead Analytical Development and product characterization for Theradaptive's recombinant proteins, medical devices, bio-scaffolds, etc. (theradaptive.com)
  • The significance of the developed method is based on the analysis of important active substance aciclovir, its impurities and preservative in pharmaceutical preparation using UHPLC system with relatively high separation temperature which leads to radical analysis time shortening up to five times and solvent saving up to ten times comparing to the conventional HPLC system using 5 μm particle packed analytical column. (rsc.org)
  • By leveraging the experience gained from developing processes for more than 75 unique biomolecules, KBI has perfected standard approaches for process development across various classes of proteins, including monoclonal antibodies. (kbibiopharma.com)
  • This session is for talks that address innovations in PAT, highlighting the development of new techniques and the application of existing techniques to new processes or problems. (aiche.org)
  • Together, they will not only develop aquathermal system pilot projects but also study the development processes surrounding them. (lu.se)
  • Together with the researchers from Delft University, they will collaborate to devise an analytical framework to examine largely bottom-up aquathermal system development processes, assess several existing or planned cases around the North Sea Region, as well as to coordinate and examine future visions of aquathermal energy development in the EU for coming decades. (lu.se)
  • We also hope that the project will create opportunities to ensure that issues of energy access and justice are tangibly integrated into planning and development processes in the EU. (lu.se)
  • Develop procedures and approaches that assure the highest scientific rigor and analytical approach. (theradaptive.com)
  • Analytical method development in pharmaceutical industry is a risk-based approaches for the assessment of the quality of drug substances and drug products based on product QTPP and CQAs. (pharmadigests.com)
  • Analytical procedure development and change management approaches are described in ICH Q14 whereas analytical procedure validation is described in ICH Q2. (pharmadigests.com)
  • With an ever-increasing awareness of the risks in pharmaceutical production and control and the lifecycle approaches being followed, greater emphasis is being placed on ensuring that the research and development of products are appropriately controlled and documented. (pharmadigests.com)
  • These objectives will be realised through an investigation into the science of enamelling, including current practice, using modem analytical facilities, available in the RTDs, and by the subsequent development of a computerised Knowledge Technology System. (europa.eu)
  • Analytical psychology, or "complex psychology", from the German: Komplexe Psychologie, is the foundation of many developments in the study and practice of Psychology as of other disciplines. (wikipedia.org)
  • 2. Purity Tests are made to ensure that all the analytical procedures are performed to allow an accurate statement of the content of impurities of an analyte. (newedgeoverseas.com)
  • Early in developing a new analytical procedure, the scientists should select the choice of analytical instrumentation and methodology based on the intended purpose and scope of the analytical method. (newedgeoverseas.com)
  • The objective of validating an analytical procedure is to demonstrate that it is suitable for its intended purpose. (newedgeoverseas.com)
  • The accuracy of an analytical procedure expresses the closeness of agreement between the value, which is accepted either as an actual conventional value or an accepted reference value, and the value found. (newedgeoverseas.com)
  • The precision of an analytical procedure expresses the closeness of agreement between a series of measurements obtained from multiple sampling of the same homogeneous sample under the prescribed conditions. (newedgeoverseas.com)
  • Other supporting analytical procedures may compensate lack of specificity of an individual analytical procedure. (newedgeoverseas.com)
  • Conducting risk assessment and evaluating prior knowledge to identify the analytical method parameters that can impact performance of the procedure. (pharmadigests.com)
  • Conducting uni- or multi-variate experiments to explore ranges and interactions between identified analytical procedure parameters. (pharmadigests.com)
  • Defining an analytical method control strategy based on enhanced procedure understanding including appropriate set-points and/or ranges for relevant analytical method parameters ensuring adherence to performance criteria. (pharmadigests.com)
  • From 2002, the development of WHO specifications follows the New Procedure , described in the Manual for Development and Use of FAO and WHO Specifications for Pesticides. (who.int)
  • Collaborate effectively with cross-functional teams including Process Development, Manufacturing, QC and Quality Assurance. (lever.co)
  • You will collaborate within your team and with other teams to improve internal platforms and deliver on partner cell line development and drug discovery projects. (hydrogengroup.com)
  • They collaborate professionally on an international level through the International Association of Analytical Psychologists (IAAP) and the International Association for Jungian Studies (IAJS). (wikipedia.org)
  • As the cell therapy industry continues to rapidly grow and evolve, the opportunity to learn from and collaborate with leading experts in the field will ensure that potency, characterisation and multi-region access are no longer bottlenecks in the cell therapy drug development pipeline. (cell-therapy-analytics-europe.com)
  • We are excited to collaborate with other researchers and proponents of aquathermal energy system development around the North Sea Region to both promote and understand the technology's possibilities, says Barry Ness. (lu.se)
  • In carrying out the optimization of the analytical method, parameters are changed individually depending on the arising interests. (pharmaguideline.com)
  • It is recommended that forced degradation be performed early in the method development lifecycle and that method parameters are suitable for mass spectrometry. (ampacanalytical.com)
  • Introducing a new cell therapy demands optimal performance in upstream and downstream processing, process development, testing, and manufacturing. (sigmaaldrich.com)
  • From early phase development, through downstream purification to large scale vaccine production: learn more about vaccine process development and application expertise. (sigmaaldrich.com)
  • Pharmaceutical drug product development can be an expensive and time consuming process. (outsourcing-pharma.com)
  • Having integrated process development and analytical development teams ensures a broad perspective to achieve product quality goals for each program. (kbibiopharma.com)
  • Analytical method development is a process whose main purpose is to prove if any analytical method in the pharmaceutical industry is suitable to be used in the measurement of API. (pharmaguideline.com)
  • Process Analytical Technology (PAT), also known as in Situ Analysis, has become a broad and integral part of the biopharmaceutical process development cycle, with rich applications in both active ingredients and formulated drug product, spanning development through commercial manufacture. (aiche.org)
  • We can provide all supporting analytical data to help ensure a smooth application process. (profarmaco.net)
  • Perform and coordinate testing to support clinical and commercial manufacturing process, process development and validation, and research and development efforts. (affyimmune.com)
  • Research and development, quality control, and quality assurance are the three central departments involved in this process. (newedgeoverseas.com)
  • Analytical method validation is a process used to prove through scientific study that the method is suitable for its intended use. (pharmadigests.com)
  • The World Bank's work in urban development aims to build sustainable cities and communities through an urbanization process that is green, inclusive, competitive, and resilient, contributing to the Sustainable Development Goal (SDG) No.11 , to the implementation of the New Urban Agenda , as well as to the World Bank's goals to end extreme poverty and boost shared prosperity. (worldbank.org)
  • The new regulations implement tools familiar from QbD into the analytical method development process. (bioeducator.eu)
  • Phase-appropriate Application of Process Analytical Technology for Early Pharmaceutical Development of Oral Solid Dosage Forms-the Case Study of Uniformity Screening of Dosage Units and Blends. (bvsalud.org)
  • Process analytical technology (PAT) in late-stage drug product development is typically used for real- time process monitoring , in-process control, and real- time release testing. (bvsalud.org)
  • Five countries10 have yet to engage in the NHO development process within the iAHO. (who.int)
  • Fill out the form below and we'll send your colleague an invitation to the "Tackling Analytical Bottlenecks in Next-Generation Drug Development" event. (technologynetworks.com)
  • There are hundreds of drug candidates to screen for purity, integrity and stability during early drug development, which can become a considerable bottleneck. (technologynetworks.com)
  • In the pharmaceutical industry, analytical method development gives important information on the potency of a drug, the drugs' bioavailability, the drugs' stability and also its effects. (pharmaguideline.com)
  • Cambrex offers a comprehensive suite of testing services for complex biopharmaceuticals including standalone analytical R&D, method validation, release testing, ICH stability, and routine QC testing. (profarmaco.net)
  • Experience in implementing ICH guideline-based stability studies and development methodologies. (theradaptive.com)
  • AMPAC Analytical development strategy involves the early adoption of forced degradation studies with the goal of every primary purity method being stability-indicating (specificity) and mass spectrometry compatible. (ampacanalytical.com)
  • From Analytical Method Development and Implementation to Analytical Method Validation and stability, AMPAC Analytical is fully equipped with fully compliant cGMP instrumentation geared toward product analysis and product release. (ampacanalytical.com)
  • These analytical figures of merit include quantification limits, detection limits, analysis time frame, operational costs and sample preparation. (pharmaguideline.com)
  • Biopharma companies at all stages of development, rely on our expertise and broad capabilities to produce the clinical trial supply of drug products they need, when they need them. (profarmaco.net)
  • The partners are all complementary to the project, involving analytical providers, a raw material supplier, an end product manufacturer and enamel contract service providers. (europa.eu)
  • If you're considering outsourcing product and analytical development, this Insight Guides provides key considerations your outsourcing partner should perform on your behalf. (outsourcing-pharma.com)
  • If you're looking to outsource drug product development to a CDMO, you need a collaborative partner who will engage you deeply to understand the unique needs of your project. (profarmaco.net)
  • We do have a range of analytical techniques that can add value to the understanding of your product. (particle.dk)
  • Any analytical method applied to a pharmaceutical product under current Good Manufacturing Practices (cGMPs) requires validation. (newedgeoverseas.com)
  • The goal of method development is to obtain an analytical method fit for its intended purpose: to measure an attribute or attributes of the drug substance or drug product with the needed specificity/selectivity, accuracy and/or precision over the reportable range. (pharmadigests.com)
  • The literature review is an important part of pharmaceutical product development demonstrating literature based knowledge and understanding of the target drug product. (pharmadigests.com)
  • The objective of this study is to find out the development and manufacturing feasibility of the product. (pharmadigests.com)
  • AMPAC Analytical (AAL) supports all analytical requirements for pharmaceutical intermediates, Active Pharmaceutical Ingredients and formulated drug product. (ampacanalytical.com)
  • Our development experts apply their ingenuity and skill to address your unique challenges. (profarmaco.net)
  • Nuclide Inventory Validation: Radiochemical Assay Data Quality and Modeling Challenges in Benchmark Models Development. (ornl.gov)
  • We argue that while some of these challenges remain unique to Cannabis, others are common to botanical-based drug development and manufacture. (researchgate.net)
  • Here is the latest news from Particle Analytical. (particle.dk)
  • Particle Analytical ApS uses cookies, including third party cookies, to improve the user experience on our website by securing functionalities, generate statistics and to save your preferences for marketing purposes. (particle.dk)
  • As a result, the Pharmaceutical industry spends enormous resources and money on their new drug development. (newedgeoverseas.com)
  • NIOSH Technical Report: Guidelines for air sampling and analytical method development and evaluation. (cdc.gov)
  • However, a major limitation of this method is its low throughput, resulting in highly inefficient method development and optimization when onboarding new molecules. (technologynetworks.com)
  • Optimization of an analytical method is done in reference to a systematic and procedural plan while making sure to critically follow all the documented steps. (pharmaguideline.com)
  • The holding of the Table became an important stage in the development of cooperation between RSUH and RAU, within the framework of which significant results were achieved in 2021-2022, including the opening of a joint center for Eurasian studies, a series of joint academic and expert events, and the organization of advanced training and educational modules for the teaching staff of RAU. (rsuh.ru)
  • Instead, you're being asked to evaluate the logical soundness of an argument of another writer and, in doing so, to demonstrate the critical thinking, perceptive reading and analytical writing skills that university faculty consider important for success in graduate school. (ets.org)
  • Conducting appropriate development studies to evaluate analytical method performance characteristics such as specificity, accuracy and precision over the reportable range (including the calibration model, limits at lower and/or higher range ends) and robustness. (pharmadigests.com)
  • The 2030 Agenda for Sustainable Development identified access to safe, effective, quality and affordable essential medicines and vaccines as central to the achievement of universal health coverage, in target 3.8 of the Sustainable Development Goals (SDGs). (who.int)
  • We have the expertise, flexibility, and resources to provide a full range of pharmaceutical API custom development services at every stage of the lifecycle. (profarmaco.net)
  • We are equipped to take on projects at any size or scale, offering established pediatric formulation and development expertise and to-scale manufacturing capabilities. (profarmaco.net)
  • With your analytical development, vendor management, and cell therapy expertise, you will leave an indelible mark on Affy. (affyimmune.com)
  • M ethod development and validation vary by application (quantitative, qualitative, etc. (ampacanalytical.com)
  • Foster a data integrity mindset within the Analytical Development/Quality Control team. (theradaptive.com)
  • The purpose of this article is to explain how you can connect an Analytical Query based on ABAP CDS views with a SAP Lumira application and expose your data with a map component. (sap.com)
  • Similar to the first article of this series, we'll reuse the analytical data model provided in my previous post explaining how to Create an analytical model based on ABAP CDS views . (sap.com)
  • The essence of these analytical tools lies in their ability to transform raw data into actionable insights. (who.int)