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provided by Outsourcing in Clinical Drug Development. A panel of experts discuss supplier identification and selection, financial considerations;
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provided by Outsourcing in Clinical Drug Development. A panel of experts discuss supplier identification and selection, financial considerations;
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strategies to formulate drug candidates with the least chance of failing in clinical development. Comes from contributing authors with experience;
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In this book, the authors discuss the principles, methodology and emerging challenges of drug development. Topics include outsourcing and;
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This two-volume set provides a full account of the entire sequence of drug development, from conceptualizing the drug, creating a library;
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Presenting applications in clinical development, pharmacokinetic/ pharmacodynamic modelling and clinical trial simulation, this reference;
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This new volume focuses on clinical biochemistry fundamentals, cell culture techniques, and drug discovery and development concepts. It;
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Aimed at those already involved in drug development or those considering entering the field, Clinical Drug Trials and Tribulations, Second;
Vergelijkbare producten zoals Clinical Drug Trials and Tribulations, Revised and Expanded
for clinical testing. It provides a thorough treatment of drug target discovery, validation, and development. The introductory chapters;
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and analyzing the results of clinical trials, and modifying a drug as necessary. Volume 2: Drug Development delves into the nitty-gritty;
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Written by a leading researcher in the field, Transporters in Drug Discovery and Development provides a comprehensive and practical guide;
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synthesize an invaluable overview of the experimental and clinical processes of anticancer drug development, creating a single indispensable;
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Elemene Antitumor Drugs: Molecular Compatibility Theory and its Applications in New Drug Development and Clinical Practice mainly;
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, lengthy development timelines, and late-stage drug failures. Novel clinical trial designs that enroll participants based on their genetics;
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process. This stage involves two processes namely, pre-clinical development and clinical phase. Drug development ensures that all parameters;
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of administration and delivery systems Noninvasive and continuous drug monitoring Regulatory path to drug product development Clinical endpoints for;
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controls by authorities. Today, the research and development of a new drug can easily consume more than $800 million and lasting between 10 and 15;
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, this volume critically highlights the multidisciplinary nature of drug development and spans the fields of pharmacokinetics, clinical;
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of the work groups, the work group guidelines and structure, and the statistical issues associated with clinical trials in clinical drug;
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It is estimated that 80 to 90% of drugs under development never make it to the marketplace due to insufficient clinical activity;
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It is estimated that 80 to 90% of drugs under development never make it to the marketplace due to insufficient clinical activity;
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in which PET offers new and unique information for the development of drugs (conception, toxicity, pharmacokinetics and metabolism, clinical;
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validation to their use in clinical development programs. Chapters are devoted to the description of the drug discovery process, to the various;
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highlighted as well. The Handbook of Phase I/II Clinical Drug Trials is your complete guide to successful early drug development.;
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clinical investigators involved in clinical trials, drug development and eventual registration of novel pharmaceuticals. Each volume;
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clinical trials and observational studies in biopharmaceutical product development. It presents the latest statistical methods for drug safety;
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, bioinformatics and machine learning approaches with nonclinical and clinical experimentation to accelerate drug development. This book discusses the;
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