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Challenges and Prospects for Clinical Trials in India: A Regulatory Perspective

 
Ali Mehdi (Author) Rahul Mongia (Author) Deepmala Pokhriyal (Author) Seema Rao (Author)
Synopsis

Clinical trials are integral to drug discovery and bringing out newer and better medicines. With the evolution of India’s disease burden as well as its pharmaceutical industry, the need for clinical trials has increased manifold. This report analyses prospects and challenges of clinical trials in India, focusing on New Chemical Entities and new drugs, and likewise proposes actionable policy recommendations for the Indian drug regulatory landscape so that the country can realise its untapped potential, while addressing concerns raised regarding the conduct and quality of clinical trials. The Government of India needs to develop a promotive ecosystem around clinical trials—now more than ever, sooner rather than later. A clear set of policy, rules and guidelines around clinical trials would be a central component in the larger strategy to address India’s public health challenges and incentivise the country’s pharmaceutical industry to mature to the next level.

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About the author

Seema Rao

Dr. Seema Rao ia consultant in tactical and combat training. She has trained the Indian Armed Forces, the paramilitary and the Police. Her research in combat training and her efforts to modernize combat training was appreciated by the Chief of Army Staff in Oct. 2001. Having trained almost every elite fighting force in the country dealing with terrorism, her exposure to the realities and horrors of the senseless extinction of human beings, along with the purposeless destruction of property is ample.

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Bibliographic information

Title Challenges and Prospects for Clinical Trials in India: A Regulatory Perspective
Format Softcover
Date published: 31.12.2017
Edition 1st ed.
Language: English
isbn 9789332704268
length 88p.