Quantitative Drug Safety and Benefit Risk Evaluation (eBook, PDF)

Practical and Cross-Disciplinary Approaches
Redaktion: Wang, William; Li, Judy; Buchanan, James; Munsaka, Melvin

• Format: PDF

Produktbeschreibung

This book provides a comprehensive coverage on safety monitoring methodologies, covering both global trends and regional initiatives. Pharmacovigilance has traditionally focused on the handling of individual adverse event reports however recently there had been a shift towards aggregate analysis to better understand the scope of product risks.

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Produktdetails

• Verlag: Taylor & Francis
• Seitenzahl: 402
• Erscheinungstermin: 30. Dezember 2021
• Englisch
• ISBN-13: 9780429950001
• Artikelnr.: 63077879

Autorenporträt

Dr. William (Bill) Wang is currently Executive Director in the department of Biostatistics and Research Decision Sciences, Merck Research Laboratories, where he has worked for 20+ years. Bill has served as the deputy topics-leader for the ICH E17 Working Group and has co-chaired the ASA Biopharmaceutical Safety Working Group. He is an elected ASA Fellow. Dr. Melvin S. Munsaka is currently Senior Director and Head of Safety Statistics at AbbVie. He has more than 25 years of industry experience. He is a member of the ASA Biopharmaceutical Safety Scientific Working Group, DIA Bayesian Scientific Working Group, and the PHUSE Safety Analytics Working Group Dr. James Buchanan, president of Covilance LLC, has 30+ years of drug safety experience in the pharmaceutical industry. He is a co-lead of the ASA Biopharmaceutical Safety Working Group and the Interactive Safety Graphics taskforce that is developing novel, open-source, interactive graphical tools to evaluate drug safety issues. Dr. Judy X. Li is currently Senior Director, Biostatistics Lead for San Diego site Bristol Myers Squibb. She also has extensive experience working at the US Food and Drug Administration as a master statistical reviewer and supervisory mathematical statistician. She is the founding co-chair of the ASA Biopharmaceutical Safety Working Group.

Inhaltsangabe

1 The Emergence of Aggregate Safety Assessment Across the Regulatory
Landscape 2 Aggregate Safety Assessment Planning in Clinical Development 3
Safety Signaling and Causal Evaluation 4 Safety Monitoring through External
Committees 5 An Overview on Statistical Methodologies for Safety Monitoring
and Benefit-Risk Assessment 6 Quantitative Methods for Blinded Safety
Monitoring 7 Bayesian Safety Methodology 8 Likelihood-Based Methods for
Safety Monitoring 9 Meta-Analysis for Drug Safety Assessment 10 Design
consideration for pragmatic trials with insight from cardiovascular outcome
trials 11 Post-market Safety Assessment Using Observational Studies and the
FDA Sentinel System 12 Analysis Considerations for Real-World Evidence and
Clinical Trials Related to Safety 13 Trends and Recent Progress in
Benefit-Risk Assessment Planning for Medical Products and Devices 14
Estimands in Safety and Benefit Risk Evaluation 15 Visual Analytics for
Safety and Benefit Risk Evaluation