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portada Benefit-Risk Assessment in Pharmaceutical Research and Development (Chapman & Hall (en Inglés)
Formato
Libro Físico
Editorial
Idioma
Inglés
N° páginas
220
Encuadernación
Tapa Blanda
ISBN13
9780367576240
N° edición
1

Benefit-Risk Assessment in Pharmaceutical Research and Development (Chapman & Hall (en Inglés)

Andreas Sashegyi (Editor), James Felli (Editor), Rebecca Noel (Editor) (Autor) · Crc Pr Inc · Tapa Blanda

Benefit-Risk Assessment in Pharmaceutical Research and Development (Chapman & Hall (en Inglés) - Andreas Sashegyi (Editor), James Felli (Editor), Rebecca Noel (Editor)

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Reseña del libro "Benefit-Risk Assessment in Pharmaceutical Research and Development (Chapman & Hall (en Inglés)"

Many practitioners in the pharmaceutical industry are still largely unfamiliar with benefit-risk assessment, despite its growing prominence in drug development and commercialization. Helping to alleviate this knowledge gap, Benefit-Risk Assessment in Pharmaceutical Research and Development provides a succinct overview of the key considerations relevant to benefit-risk assessment across the pharmaceutical R&D spectrum, from early clinical development to late-stage development to regulatory review to post-launch assessment.The book first presents interpretations of benefit and risk in the context of a molecule moving from preclinical evaluation into its early testing in humans. It next considers benefit and risk characterization and assessment during a molecule's journey from its clinical evaluation in humans through its submission to regulators for marketing approval. Throughout these sections, the book offers insight into the role of benefit-risk assessment in heightening understanding among key stakeholders by shaping questions and guiding discussions among scientists, physicians, developers, and regulatory agencies. The book also focuses on a molecule's entry into the marketplace as a drug available for consumption by people. It explores the role of benefit-risk assessment as the relevance of carefully collected clinical efficacy and safety metrics fades in the wake of real-world use and evidence of effectiveness and safety.Bringing together the expertise of 15 contributors from academia and the industry, this book offers an easy-to-read guide to the various facets of benefit-risk assessment in the major stages of pharmaceutical R&D. Suitable for those in both technical and managerial roles, it enables readers to communicate more effectively across their development chain as well as rationally and thoughtfully embed benefit-risk assessment into their R&D processes.

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