Press release |

MSF responds to media reports on Indian Government’s verbal assurance to US groups to discontinue the use of compulsory licence

Photograph by Ravi Mishra
MSF Nurse Jijo Xavier checks the vitals of a patient at the PL Sharma District Hospital in Meerut city where MSF runs a Hepatitis C project in collaboration with the National Health Mission, providing free services.

New Delhi, 15 March 2016 — Médecins Sans Frontières (MSF) is deeply concerned about the recent revelations in the media that a US industry lobby group – the US India Business Council (USIBC) and US Chamber of Commerce – has received verbal, private assurances from Indian officials that it will not use ‘compulsory licensing’ (CL) for commercial purposes.

The statements are part of USIBC’s submission to USTR’s (US Trade Representative) annual Special 301 report. Many US industries, in particular the pharmaceutical industry, use the report to condemn governments which employ intellectual property (IP) systems that do not match intellectual property laws and practices in the United States. Current US intellectual property laws enable drug makers to charge exorbitant prices for medicines, such as Gilead Sciences, which charge up to US$1,000 a pill for new hepatitis C drug sofosbuvir.

India—the world’s principal producer and supplier of quality generic medicines, including for US-funded treatment programs like PEPFAR that support antiretroviral treatment in developing countries— has in recent years repeatedly been singled out by the US government and the multinational pharmaceutical industry for insufficient enforcement of intellectual property.


MSF responds with the below 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. 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 HIV and hepatitis C – and on critical vaccines like the pneumococcal conjugate vaccine (PCV).

“Compulsory licences can be granted on many grounds including but not limited to: non-working of a patent, addressing anti-competitive conduct, reducing prices of unaffordable medicines and addressing public health emergencies. Yet, the USIBC and other pharma lobbies are working to discourage the Indian government, its patent authorities and courts from using these legal tools available under both Indian 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. Such a commitment will encourage multinational drug companies to start charging unaffordable prices to Indian patients and governments across the developing world, further undermining access to critical, and life-saving products.”

- Leena Menghaney, Regional Head-South Asia, MSF Access Campaign