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Titlebook: Benefit-Risk Assessment of Medicines; The Development and James Leong,Sam Salek,Stuart Walker Book 2015 Springer International Publishing

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发表于 2025-3-21 18:15:56 | 显示全部楼层 |阅读模式
期刊全称Benefit-Risk Assessment of Medicines
期刊简称The Development and
影响因子2023James Leong,Sam Salek,Stuart Walker
视频video
发行地址Examines current approaches for the benefit-risk assessment of medicines and the acceptability of a “universal framework” by regulatory agencies and pharmaceutical companies.Presents the development a
图书封面Titlebook: Benefit-Risk Assessment of Medicines; The Development and  James Leong,Sam Salek,Stuart Walker Book 2015 Springer International Publishing
影响因子.This book proposes and investigates a universal framework, and accompanying documentation system, to facilitate and catalogue benefit-risk decisions; a valuable addition to the benefit-risk toolbox..Over the past decade, pharmaceutical companies and regulatory agencies have been reviewing the benefit-risk assessment of medicines with a view to developing a structured, systematic, standardized approach. Examining the evaluation of such an approach by several mature regulatory authorities ensures that the reader gains a unique insight into the ongoing debate in this area..The field of benefit-risk assessment continues to evolve at a rapid pace due to political and societal pressure, as is reflected in the recent FDA PUDFA agreement as well as in the EMA 2015 Roadmap. Rather than provide a comprehensive snap-shot of this constantly changing environment, this book evaluates selected current approaches to benefit-risk assessment. The strengths and weaknesses of publicly available documents in communicating benefit-risk decisions to stakeholders are reviewed and these evaluations are used to inform development of a prospective framework that could be used to harmonise procedures globall
Pindex Book 2015
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,Benefit–Risk Assessment of Medicines by Pharmaceutical Companies and Regulatory Authorities,es bear the responsibility to ensure that the approved products demonstrate the efficacy and safety as shown in the clinical trial data submitted. However, such regulatory decisions are largely based on clinical judgment and the local medical context in each country. In a bid to minimize subjectivit
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,Implementation of the Benefit–Risk Assessment Template by Mature Agencies, Chap. . showed that both regulatory agencies and pharmaceutical companies believe that a benefit–risk framework would enhance the quality (transparency and consistency) of decision-making; provide documentation for a systematic, structured discussion; and act as a tool for communication. A tool was
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,Communicating Benefit–Risk Decisions by US FDA, EMA, TGA, and Health Canada,nd the separate assessment of benefits and risks, the emphasis is now on the balance between the two, having to justify the potential harms in view of the efficacy claims. In a changing society where the demand is for transparency of such decision-making processes, there is now a major challenge to
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