The organisation, also known as Doctors Without Borders, accused US India Business Council (USIBC) and other pharma lobbies for working to discourage government and courts in India from using legal tools available under both domestic patent law and international trade rules.
"Any commitment to stop granting compulsory licences and enforce patent law safeguards will defeat the legislative intent of the public health safeguards that are enshrined in India's patent law, and which were globally welcomed by the United Nations, MSF and developing country governments in 2005," MSF Access Campaign Regional Head-South Asia Leena Menghaney said in a statement.
"For almost a decade, India has championed affordable access to medicines by setting strict patentability standards and issuing compulsory licences, both of which are legal tools available to all governments under the TRIPS Agreement," Menghaney said.
These legal tools have never been as crucial as they are today as the Indian patent office considers patent applications on new life-saving medicines to treat infectious diseases - such as sofosbuvir or dolutegravir for hepatitis C and HIV- and on critical vaccines like the pneumococcal conjugate vaccine, she added.
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"Despite compulsory licensing denials, industry continues to be concerned by the potential threat of compulsory licensing. The Government of India has privately reassured...(that) it would not use Compulsory Licenses for commercial purposes," the USIBC had said in the submission to the US Trade Representative.
The Indian Patent Office had granted compulsory licensing for the first time in March 2012 to permit Hyderabad-based Natco Pharma to manufacture and sell cancer-treatment drug Nexavar at a fraction of the price charged by its patent-holder Bayer Corporation.