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Regulation of medicines and medical devices : Medical a
Product List : Total 41 results
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Balancing Wealth and Health: The Battle over Intellectual Property and Access to Medicines in Latin America
This book focusses on the debates concerning aspects of intellectual property law that bear on access to medicines in a set of developing countries. Specifically, the contributors look at measures that regulate the...

Hardback: Rs. 8,100.00
Identity, Invention, and the Culture of Personalized Medicine Patenting
By Shubha Ghosh
What are the normative implications of patenting in the area of personalized medicine? As patents on genes and medical diagnoses have increased over the past decade, this question lies at the intersection of...

Paperback / softback: Rs. 2,399.00
Medicinal Product Liability and Regulation
By Richard Goldberg

Hardback: Rs. 15,600.00  Rs. 13,260.00
Unhealthy Pharmaceutical Regulation
By Davis, Courtney& Abraham, John
This is the first book to examine how effectively American and supranational EU governments have regulated innovative pharmaceuticals during the last 30 years regarding public health. It explains why pharmaceutical...

Hardback: Rs. 10,799.00  Rs. 9,179.00
Informal Norms in Global Governance
By Hein, Wolfgang& Moon, Suerie
After a decade of heated political contestation, an informal but robust and powerful global norm had emerged that all people should have access to essential medicines. This book recounts the remarkable story of the...

Hardback: Rs. 17,400.00  Rs. 14,790.00
Drug & Device Product Liability Litigation Strategy
By Herrmann, Mark& Alden, David B.
Drug & Device Product Liability Litigation Strategy provides useful practice pointers and overall strategic guidance for attorneys involved in product liability litigation for prescription drugs and medical devices.

Paperback: Rs. 25,200.00  Rs. 21,420.00
Nonclinical Safety Assessment: A Guide to International Pharmaceutical Regulations
Providing a comprehensive, international overview of the regulatory requirements for safety assessment for new drug approvals, each chapter in Nonclinical Safety Assessment is written by experts who have direct,...

Hardback: Rs. 12,000.00
FDA Oversight of Medical Devices: Efforts & Developments
The FDA is responsible for overseeing the safety and effectiveness of medical devices sold in the United States. New devices are generally subject to FDA review via the 510(k) process, which determines if a device is...

Hardback: Rs. 10,400.00
Patently Innovative: How Pharmaceutical Firms Use Emerging Patent Law to Extend Monopolies on Blockbuster Drugs
By Ron A. Bouchard
Patently innovative provides a review of the importance of traditional patent law and emerging linkage regulations for pharmaceutical products on the global stage, with a focus on the linkage regime in Canada. The...

Hardback: Rs. 12,500.00