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Paperback • 2017
Pages: 84
ISBN: 9789332704251
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Academic Foundation

International Cooperation for Registration of Medicines

Opportunities for India

Ali Mehdi‚ Vasudha Wattal‚ Pallavi Joshi‚ Aashna Arora

About the Book

To tackle the rising burden of disease, disability and premature deaths, the demand for newer and better treatment is more than ever. Drug registration is a critical step for the introduction of medicines in a country. There has been a great deal of international interaction and cooperation in the area of public health, particularly since the conception of the Millennium Development Goals. However, international cooperation vis-à-vis mechanisms to achieve shared goals of public health are still very limited. Regulation of drugs, more specifically drug registration, is one such neglected area. This report, the first-of-its-kind, based on extensive desk and field research in 4 Indian states—Maha-rashtra, Karnataka, Gujarat and Telangana—and 7 countries—USA, UK, Switzerland, Germany, South Africa, Singapore and Indonesia—incorporates views of more than 150 stakeholders to identify lessons as well as opportunities for the Government of India in its effort to address challenges of drug regulation in particular, and public health more generally, in the country.

Praise for this book

<p>“Through a thoughtful review of various countries’ drug registration procedures, this report summarizes international cooperation initiatives, and various opportunities critical in reestablishing India as a leader in pharmaceutical development. This report will be vital for government and private sector efforts to modernize India’s drug registration processes.”<br /> <strong>— Mark Barnes, </strong>J.D., LL.M<br /> <strong>&nbsp; &nbsp; &nbsp;Barbara Bierer, </strong>M.D.,<br /> &nbsp; &nbsp; Multi-Regional Clinical Trials Center of Brigham and<br /> &nbsp; &nbsp; Women’s Hospital and Harvard University</p> <p>&nbsp;</p> <p>“This is an excellent and timely report from an expert group that should be very useful to the Indian government as it considers possible improvements in its systems for review and approval of drug products.”<br /> <strong>— Richard Kingham</strong><br /> &nbsp; &nbsp;&nbsp;Senior Counsel of Covington &amp; Burling LLP<br /> &nbsp; &nbsp;&nbsp;in Washington, DC, and&nbsp;London and<br /> &nbsp; &nbsp;Adjunct Professor at the Georgetown University Law Centre</p> <p>&nbsp;</p> <p>“A hallmark of maturing drug regulatory systems is ongoing review and refinement of regulatory requirements. Stakeholder engagement is crucial to those efforts; this paper provides an important overview to support efforts for increased international cooperation throughout India’s drug registration system.”<br /> <strong>— Susan Winckler</strong><br /> &nbsp; &nbsp; &nbsp;President of Leavitt Partners Consulting, USA</p> <p>&nbsp;</p> <p>“A team of young researchers have made a noteworthy effort to document the current practices in a few markets and identified gaps to improve the registration process in India.”<br /> <strong>— D.G. Shah</strong><br /> &nbsp; &nbsp; Secretary General, Indian Pharmaceutical Alliance</p>

About the Author(s) / Editor(s)

<p><strong>Ali Mehdi </strong>established and leads the Health Policy Initiative at ICRIER. His research interests include—the process, design and assessment of health policies; prevention of chronic diseases along with policy instruments and institutional design for its promotion; social determinants of health; metrics of health inequities; health financing, governance and manpower; fertility and mortality; demographic dividend; drug regulation. A couple of his books are in the pipeline—India Health Report 2018 (Oxford University Press), A Shot of Justice (2 volumes) (Oxford University Press), Chronic Diseases in South Asia (Springer), Freedoms and Fragility: The Challenge of Job Creation in Kashmir, India (Routledge). Ali did his MA at the University of Freiburg, Germany and completed his PhD at Humboldt University in Berlin. He can be reached at</p> <p>&nbsp;</p> <p><strong>Vasudha Wattal</strong> is a Research Associate at ICRIER, and has been associated with the Health Policy Initiative since its inception in 2014. She is specifically involved in the drug regulatory project and has contributed to various publications developed under this research program. She has also co-authored a number of opinion pieces and journal articles on several policy issues such as drug regulation, economics of drug pricing and air pollution. &nbsp;Her research interests include, economics of competition, economics of health and behavioural economics. Vasudha holds a Masters and an M.Phil. Degree in Economics.</p> <p>&nbsp;</p> <p><strong>Pallavi Joshi </strong>is a Research Associate at ICRIER, and is working on governance and regulatory aspects of healthcare sector and pharmaceutical industry, for publications under Health Policy Initiative. Previously, she has worked with Competition Commission of India, where she was involved in analysing competition issues in various sectors, in particular—healthcare sector, and pharmaceutical industry. She has also worked with Standard &amp; Poor’s Capital IQ, a business research firm. Her core areas of interest include development economics, health economics, pharmaceutical regulation, behavioural economics, and competition law. She holds a Masters degree in Economics.</p> <p>&nbsp;</p> <p><strong>Aashna Arora </strong>is a Consultant at ICRIER under the Health Policy Initiative. Her interest areas include health economics, environmental economics, trade and economics, public policy and ethics in policymaking. She has a passion to work for policy oriented research on issues that impact public health and access to health and medicines in India. Previously, she has worked at KPMG as a Business Associate in the Research, Analysis and Knowledge unit and interned with the Ministry of Health and Family Welfare. She holds a Masters degree in Economics.</p>

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