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Beschreibung
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, from early clinical development to late-stage development to regulatory review to post-launch assessment. Suitable for those in b
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, from early clinical development to late-stage development to regulatory review to post-launch assessment. Suitable for those in b
Über den Autor

Andreas Sashegyi is a senior research advisor in the biometrics organization at Eli Lilly and Company, where he divides his time between therapeutic compound support and work in the Benefit Risk Advisory Group. Dr. Sashegyi's research focuses on the integrated analysis of benefits and risks in pharmaceutical research and development. He received a PhD in biostatistics from the University of Waterloo.

James Felli is a research fellow in the area of drug disposition at Eli Lilly and Company. Dr. Felli is a fellow and current president of the Society of Decision Professionals and an active member of the Decision Analysis Society of INFORMS and the Decision Analysis Affinity Group. His research focuses on developing new benefit-harm models and visualizations, modeling and analyzing stochastic multicriteria decision problems, enriching communication between analysts and nonanalysts, and developing new methods of multidimensional data visualization. He received a PhD in industrial engineering and management science from Northwestern University.

Rebecca Noel is a senior research scientist at Eli Lilly and Company. Dr. Noel is the chair of the Drug Information Association working group for benefit-risk assessment and serves on the Centre for Innovation in Regulatory Science's Task Force on Benefit-Risk Assessment and the Innovative Medicines Initiative. Her research focuses on developing and promoting systematic approaches to benefit-risk assessment. She received a DrPH in international health and epidemiology from the University of Alabama at Birmingham.

Inhaltsverzeichnis

Early Clinical Development: Pharmaceutical Benefit-Risk Assessment in Early Development. Full Clinical Development: Key Questions, Issues, and Challenges in Benefit-Risk Assessment in Full Clinical Development. The Clinical Aspects of Benefit and Risk. Quantifying Patient Preferences to Inform Benefit-Risk Evaluations. Benefit-Risk Modeling of Medicinal Products: Methods and Applications. Benefit-Risk Communication: Learning from Our Past and Creating Our Future. Regulatory Review and Policy: Policy Considerations and Strategic Issues Regarding Benefit-Risk. Systematic Approaches to Benefit-Risk Assessment. Post-Launch Assessment: Considerations and Strategies for Benefit-Risk Assessment in the Real World Setting. Benefit-Risk Assessment and the Payer Perspective. Epilogue. Glossary. Index.

Details
Erscheinungsjahr: 2020
Fachbereich: Wahrscheinlichkeitstheorie
Genre: Importe, Mathematik
Rubrik: Naturwissenschaften & Technik
Medium: Taschenbuch
ISBN-13: 9780367576240
ISBN-10: 0367576244
Sprache: Englisch
Einband: Kartoniert / Broschiert
Redaktion: Sashegyi, Andreas
Felli, James
Noel, Rebecca
Hersteller: Chapman and Hall/CRC
Verantwortliche Person für die EU: Libri GmbH, Europaallee 1, D-36244 Bad Hersfeld, gpsr@libri.de
Maße: 234 x 156 x 12 mm
Von/Mit: Andreas Sashegyi (u. a.)
Erscheinungsdatum: 30.06.2020
Gewicht: 0,345 kg
Artikel-ID: 133318717

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