did-you-know? rent-now

Amazon no longer offers textbook rentals. We do!

did-you-know? rent-now

Amazon no longer offers textbook rentals. We do!

We're the #1 textbook rental company. Let us show you why.

9780470748121

Benefit-Risk Appraisal of Medicines: A systematic approach to decision-making

by ; ; ;
  • ISBN13:

    9780470748121

  • ISBN10:

    0470748125

  • Format: eBook
  • Copyright: 2009-08-01
  • Publisher: Wiley
  • Purchase Benefits
  • Free Shipping Icon Free Shipping On Orders Over $35!
    Your order must be $35 or more to qualify for free economy shipping. Bulk sales, PO's, Marketplace items, eBooks and apparel do not qualify for this offer.
  • eCampus.com Logo Get Rewarded for Ordering Your Textbooks! Enroll Now
List Price: $109.95
We're Sorry.
No Options Available at This Time.

Summary

Benefit-risk assessment is at the centre of the approval process for every new medicine. The ability to assess the risks of a new medicine accurately and to balance these against the benefits the medicine could bring is critical for every regulatory authority and pharmaceutical company. Despite this there are very few tried and tested evaluative models currently available. The authors of this book have developed a new, pioneering tool for the assessment of benefits and risks for new medicines in development. This model utilises a multi-criteria decision analysis which involves selecting, scoring and weighting key benefit and risk attributes and leads to an overall appraisal of benefits and risks of medicines. Benefit-Risk Appraisal of Medicines establishes the background and criteria required to assess benefit and risk in general and reviews the current practices by regulatory authorities and the pharmaceutical industry, including those models currently available. It outlines the development and evaluation of the authors' new model and analyses the implications of its implementation. Describes an innovative, systematic model which leads to transparent and responsible benefit-risk decision making Contributes important ideas to the debate on benefit-risk appraisal Provides a future framework for benefit-risk appraisal of medicines Benefit-Risk Appraisal of Medicines covers the entire process from the discovery of new medicines to their marketing and is ideal for all those who work in the pharmaceutical industry and regulatory authorities,, as well as post-graduate students of pharmaceutical medicine and clinical pharmacology.

Table of Contents

Foreword
Preface
Concept and Scope of Benefit-Risk Evaluation of Medicines
Historical backgroun
The regulatory systems for assessing medicines
Benefit-risk assessment: definitions
Views and perceptions of benefits and risks of medicines
Stages and concepts in benefit-risk assessment
Benefit-risk assessment: the current regulatory environment
Benefit-risk assessment in other disciplines
Specific methods and models for benefit-risk assessment
Discussions with stakeholders on the concepts and models for benefit-risk evaluation
Criteria for a Benefit-Risk Model: a Conceptual Framework
Introduction
Regulatory guidelines on benefit and risk criteria
Identification, definition and rationale of relevant benefit and risk criteria
Verification of the list of benefit and risk criteria by means of a survey
Review of the Current Benefit-Risk Assessment Models
Background
Evaluation of the existing benefit-risk assessment models
Review of models in single clinical trials and for specific medicines
Conclusion
Newer models
Defining a Systematic Approach to Decision Making
Introduction
Objectives and features of the ideal model for benefit-risk assessment
The use of decision-analysis techniques for the development of the new model
Development and Application of a Benefit-Risk Assessment Model Based on Multi-Criteria Decision Analysis
Introduction
Conceptualization of the new model
Reasons for using decision analysis techniques in the new model
The use of MCDA in the new model
Development of the new model
Applicability of the new model
Summary
Review of the MCDA model
A Future Framework for Benefit-Risk Appraisal of Medicines
Background
Development of a benefit-risk framework for regulatory review of new medicines
Prerequisites of a benefit-risk framework for the registration of a new medicine
Current status of benefit-risk assessment among companies and agencies
Constructing a benefit-risk framework
Conclusion
Appendices
Summary Reports of the CMR International Institute for Regulatory Science March 2004 and June 2005 Workshops on Benefit-Risk
Office of Health Economics Briefing: Challenges and Opportunities for Improving Benefit-risk Assessment of Pharmaceuticals from an Economic Perspective - James Cross and Louis Garrison (August 2008)
Reflection Paper on Benefit-risk Assessment Methods in the Context of the Evaluation of Marketing Authorisation Applications of Medicinal Products for Human Use - Committee for Medicinal Products for Human Use (March 2008)
Commentaries on 'A Quantitative Approach to Benefit-risk Assessment of Medicines' Pharmacoepidemiology and Drug Safety, 2007, 16
Forum on Benefit: Risk Decision Analysis - Summary of
Discussions and Recommendations - MHRA (September 2008)
References
Index
Table of Contents provided by Publisher. All Rights Reserved.

Supplemental Materials

What is included with this book?

The New copy of this book will include any supplemental materials advertised. Please check the title of the book to determine if it should include any access cards, study guides, lab manuals, CDs, etc.

The Used, Rental and eBook copies of this book are not guaranteed to include any supplemental materials. Typically, only the book itself is included. This is true even if the title states it includes any access cards, study guides, lab manuals, CDs, etc.

Rewards Program