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Pharmaceutical Regulatory Environment

Challenges and Opportunities in the Gulf Region

  • Book
  • © 2015

Overview

  • Examines the regulatory review practices in the seven Gulf Cooperation Council states, namely Kuwait, Iraq, Bahrain, Oman, Qatar, Saudi Arabia and the United Arab Emirates

  • Compares national metrics with those of the harmonised centralised review procedure, for companies wishing to gain market approval for new drugs in the region

  • Describes the current strategies and future opportunities for an improved regulatory environment in the Gulf region

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Table of contents (12 chapters)

Keywords

About this book

This book compares national and centralised procedure practices and key performance metrics, including current approval times, review practices and pharmacovigilance standards, in the seven Gulf States. Opportunities for an improved regulatory system are identified, which, if fully implemented, could have a significant impact on patients’ access to new medicines.

The Persian Gulf represents the next growth market for the global biopharmaceutical industry but to date there has been limited information about the regulatory review processes employed in these countries. A thorough examination of the strategies currently being implemented by the Gulf States is considered critical to the future regulatory environment in this region.

Pharmaceutical Regulatory Environment: Challenges & Opportunities in the Gulf Region is a must read for those interested in pharmaceutical regulation in the Gulf region.


Authors and Affiliations

  • Regulatory Affairs Consultant Executive Directive, Kuwait Advancement for Conference and Exhibition Management Est., Kuwait City, Kuwait

    Reem K. Al-Essa

  • Ministry of Health, Directorate General of Pharmaceutical Affairs and Drug Control, Muscat, Oman

    Mohammed Al-Rubaie

  • Founder of Centre for Innovation in Regulatory Science, London, United Kingdom

    Stuart Walker

  • University of Hertfordshire, Department of Pharmacy, School of Life and Medical Sciences, Hatfield, United Kingdom

    Sam Salek

About the authors

Reem Al-Essa BPharm MSc PhD was the Drug Registration and Release Superintendent for six years of her 12 years experience with Ministry of Health, Kuwait. During this period she completed her MBA with distinction. She later undertook the EU2P MSc in Pharmacovigilance and Pharmacoepidemiology. Dr Al-Essa has published six journal articles and abstracts related to pharmaceutical regulation in the Gulf region.

Mohammed Hamdan Al-Rubaie BPharm MSc PhD is the Director of Drug Control, Directorate General of Pharmaceutical affairs and Drug Control, Oman Ministry of Health.He is a member of the GCC Central Registration Committee, and actively involved in many other GCC committees and working groups for the drafting of the GCC pharmaceutical regulations and policies. Dr Al-Rubaie was instrumental in forming the Pharmaceutical society in Oman and chaired it from 2010-2011.

Stuart Walker BSc, PhD, MFPM FRSC FIBiol, FRCPath, is the Founder of the Centre for Medicines Research International, the Centre for Innovation in Regulatory Science and Professor of Pharmaceutical Medicine, University of Wales, Cardiff. During his research career in academia & industry, he has supervised many PhD programmes in clinical development, regulatory policies, the benefit/risk assessment of medicines and health technology assessment, co-authored 280 research papers and edited 25 books. He is frequently involved in the organisation of international meetings on key issues that concern the regulatory review of medicines and has lectured extensively throughout Europe, the USA, the Asia-Pacific Region, Latin America and the Middle East.

Sam Salek PhD RPh FFPM MRPSGB MCMS FESCP is Professor of Pharmacoepidemiology at the University of Hertfordshire, Hatfield, visiting Professor at the Estate of Hessen, Germany, and Director of the Institute for Medicines Development, Cardiff, UK. Professor Salek’s research focuses mainly on four areas: development and application of patient-reported outcome measures; drug safety evaluation and pharmacovigilance; pharmacoeconomics and economic evaluation of healthcare; and pharmaceutical regulation & medicines development in the mature and emerging markets. He has published 19 books and 600 journal articles and abstracts. Professor Salek is a member of five Editorial Boards and an active member of several societies.

Bibliographic Information

  • Book Title: Pharmaceutical Regulatory Environment

  • Book Subtitle: Challenges and Opportunities in the Gulf Region

  • Authors: Reem K. Al-Essa, Mohammed Al-Rubaie, Stuart Walker, Sam Salek

  • DOI: https://doi.org/10.1007/978-3-319-17590-4

  • Publisher: Adis Cham

  • eBook Packages: Medicine, Medicine (R0)

  • Copyright Information: Springer International Publishing Switzerland 2015

  • Hardcover ISBN: 978-3-319-17589-8Published: 21 May 2015

  • Softcover ISBN: 978-3-319-36010-2Published: 09 October 2016

  • eBook ISBN: 978-3-319-17590-4Published: 06 May 2015

  • Edition Number: 1

  • Number of Pages: XIII, 236

  • Number of Illustrations: 79 illustrations in colour

  • Topics: Public Health, Pharmacotherapy

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