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International Cooperation, Convergence and Harmonization of Pharmaceutical Regulations: A Global Perspective provides the current status of the complex and broad phenomenon of cooperation, convergence and harmonization in the pharmaceutical sector (Part I), thoroughly evaluates its added value and its critical parameters and influencing factors (Part II) in order to recommend actions and measures to support the next steps for cooperation, convergence and harmonization (Part III). All of these recommendations in the book support the establishment of a better coordinated global pharmaceutical system which represents the best realistic alternative to fulfill the objective to establish a global coalition of regulators and to respond to an increased demand to further cooperation in the pharmaceutical sector. This proposed framework, which leverages all of the ongoing positive cooperation initiatives and uses as foundations all of the numerous harmonization projects developed over the years, presents advantages for all stakeholders and would definitively have significant added value to the promotion and protection of global public health.
- The status of all major worldwide harmonization and cooperation initiatives (at bilateral, regional, and global levels)
- The value of cooperation in the pharmaceutical sector and the driving factors behind harmonization
- The proposition of a structure for the global pharmaceutical system and timely recommendations for enhancing international cooperation, as well as further discussion and policy changes in this area
- Sales Rank: #3738191 in Books
- Published on: 2013-12-24
- Original language: English
- Number of items: 1
- Dimensions: 9.00" h x .98" w x 6.00" l, 2.08 pounds
- Binding: Hardcover
- 376 pages
Review
“…thoroughly covers the current state of international cooperative initiatives, underlying principles, why cooperation is important, and productive objectives for the future… This book has been selected for The First Clinical Research Bookshelf Essential reading for clinical research professionals.”--Journal of Clinical Research Best Practices, July 2014
From the Back Cover
Globalization is a reality of the 21st century.� The development, manufacture and distribution of medicines have been internationalized.� This increased globalization has fundamentally changed the environment for regulating medicines and created unique regulatory challenges for all stakeholders.� The regulatory paradigm has indeed changed from national to international and international pharmaceutical norms and standards are more important than ever before.� International cooperation, convergence and harmonization of pharmaceutical regulations has become the only clear choice to meet the fundamental human right to have access to high quality, safe and effective medicines in both developed and developing countries.
In this context, many cooperative initiatives have been established at the bilateral, regional and global levels and harmonization efforts have been enhanced.� All of these initiatives have taken a variety of forms, from informal cooperation to full integration of regulatory systems.
International Cooperation, Convergence and Harmonization of Pharmaceutical Regulations: A Global Perspective provides the current status of this complex and broad phenomenon of cooperation, convergence and harmonization in the pharmaceutical sector (Part I), thoroughly evaluates its added value and its critical parameters and influencing factors (Part II) in order to recommend actions and measures to support the next steps for cooperation, convergence and harmonization (Part III).� All of these recommendations in the book support the establishment of a better coordinated global pharmaceutical system which represents the best realistic alternative to fulfil the objective to establish a global coalition of regulators and to respond to an increased demand to further cooperation in the pharmaceutical sector.� This proposed framework, which leverages all of the ongoing positive cooperation initiatives and uses as foundations all of the numerous harmonization projects developed over the years, presents advantages for all stakeholders and would definitively have significant added value to the promotion and protection of global public health.
This book features:
- The status of all major worldwide harmonization and cooperation initiatives (at bilateral, regional, and global levels)
- The value of cooperation in the pharmaceutical sector and the driving factors behind harmonization
- The proposition of a structure for the global pharmaceutical system and timely recommendations for enhancing international cooperation, as well as further discussion and policy changes in this area
About the Author
Dr. Pierre-Louis Lezotre specializes in global regulatory strategy, and is recognized for his passion and expertise
on international cooperation, convergence, and harmonization of regulations for pharmaceutical
and biotechnology products. He has worked in different cultural environments and lived in
both Europe and the United States.
Dr. Lezotre studied biology (University of Sciences, Saint-Etienne, France)
and drug development (University of Pharmacy, Montpellier, France) from
1992 to 1998. He then received his Master in Regulatory Sciences in 1999 (University
of Pharmacy, Lille, France). He also recently completed his PhD in Law with honors (Doctoral
School of “Law, Politics and Management,” University of Law, Lille, France).
Since 1998, Dr. Lezotre has worked for several international pharmaceutical and biotechnology
companies, with increasing levels of responsibility. He has served as a regional and
then global regulatory leader for small molecule and biologic/biotech programs in various
stages of research and development (from early discovery to life cycle management). He
successfully led many global regulatory teams in supporting global registrations of major
products and numerous development projects in several therapeutic areas, including
dermatology, urology, neurology, and pain. He has been responsible for communications
with worldwide Drug Regulatory Authorities and has also worked with external partners/
companies through co-development agreements and business development programs.
Dr. Lezotre has recently been invited to teach courses on international regulation in the
Regulatory Sciences programs of the University of Southern California (USC).
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