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Pharmacology in Pharmaceutical Development: Approval and Post Marketing Surveillance, Second Edition covers safety pharmacology from the regulatory;
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of nanomaterials are discussed with a focus on the safety and pharmaceutical considerations of nanomaterials in translational development. The;
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innovative products and solutions in pharmacology. Interdisciplinary in content it is of interest to those who are involved in the development;
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at safety issues in ion channel drug development. For medicinal and pharmaceutical chemists, biochemists, molecular biologists and those;
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across the world, on various topics related to pharmaceutical drug development. For students and researchers in the fields of pharmacology;
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personnel, discovery toxicologists, and safety scientists, drug development professionals, and pharmaceutical scientists.;
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of clinical pharmacology drug development, regulatory applications, and the design and analysis of bioequivalence trials are established, they move on;
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Medicinal or pharmaceutical chemistry is a scientific discipline at the intersection of chemistry and pharmacology involved with designing;
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Medicinal or pharmaceutical chemistry is a scientific discipline at the intersection of chemistry and pharmacology involved with designing;
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Advanced Issue Resolution in Safety Pharmacology not only discusses unique issues that may emerge during the development of new;
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recent successful new drug applications. Compiling key issues and current research on safety, efficacy, and clinical pharmacology, and PK-PD;
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aspects is critical for students in the areas of pharmaceutical medicine, clinical research, pharmacology and pharmacy, as well as professionals;
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set the stage by describing the general role of statistics. Once the foundation of clinical pharmacology drug development, regulatory;
Vergelijkbare producten zoals Bioequivalence and Statistics in Clinical Pharmacology
authors set the stage by describing the general role of statistics. Once the foundation of clinical pharmacology drug development, regulatory;
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is adopted globally by both individuals and organizations working within pharmaceutical research and development, manufacture, and testing worldwide;
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Pharmaceutical product development is a multidisciplinary activity involving extensive efforts in systematic product development and;
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, new chapters regarding safety pharmacology, juvenile studies, the health safety assessment of pharmaceuticals, and health assessment;
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, new chapters regarding safety pharmacology, juvenile studies, the health safety assessment of pharmaceuticals, and health assessment;
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This revised and extended second edition focuses on current and emerging topics in drug development, their molecular mechanisms of action;
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handbook covers essential fields in pharmacology, from drug development to cancer and gene therapy. The articles are uniformly structured for ease;
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ALS. Reviewing fundamentals and offering guidelines for drug discovery and development, this book is a practical guide from the safety assessment to;
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capabilities. Pharmacology lies at the heart of biomedical science, linking together pharmaceutical chemistry, physiology, and pathology. Comprehensive;
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individualization of patient therapy and contemporary drug development. This well-regarded survey continues to focus on the basics of clinical pharmacology;
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Practical Pharmacology for the Pharmaceutical Sciences is a lab survival guide for those studying Pharmacology, providing hands-on advice;
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Pharmaceutical policy is a field which deals with the development, use and provision of medications within a healthcare system. It;
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high priority during both development and post-approval monitoring. Integrated Cardiac Safety provides necessary guidance and methodology for;
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. Pharmacokinetics (PK) and pharmacodynamics (PD) comprise traditionally distinct disciplines within pharmacology, the study of the interaction of drugs with;
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