According to Matthew Kavanagh of Health GAP (Global Access Project), Indias adoption and one-time use of compulsory licensing and Section 3(d) of the Indian Patents Act are TRIPS-compliant and do not justify elevation of India on the USs 2014 Special 301 Watchlist.
India has been on the US priority watch list since 1974. The Special 301 report is an annual review conducted by the Office of the United States Trade Representative (USTR), which identifies trade barriers to US companies and products due to ineffective IP laws of other countries. The US is expected to take a call on imposing trade sanctions by next month.
Kavanagh also wrote, in his submission to the USTR, that US Presidents Emergency Plan for AIDS Relief and US global AIDS programmes are dependent for success on continued, robust Indian generic production of AIDS drugs through continued Indian use of WTO-compliant legal flexibilities. Listing India on the 301 Watch List would undermine President Obamas declared priority of creating an AIDS Free Generation, waste US taxpayer funds, and imperil the PEPFAR programme, he added.
India faces an imminent threat of being downgraded to a priority foreign country by the US, based on allegations made by PhRMA and other American trade associations attacking India's IP regime, particularly its issuance of a compulsory licence on a Bayer cancer medicine and the adoption of section 3(d) to the Indian Amended Patents Act and its Supreme Court decision thereunder denying a patent on a Novartis medicine.
The USTR can impose higher duties or restrictions on import of goods and services into the country for a certain period of time if India is tagged as priority foreign country. With the US accounting for around 12% of India's exports, it will impact the country's trade balance. Under the US Trade Act, a priority foreign country is a tag given to the worst offenders of patent rights and IP protection. The only country on the list, currently, is Ukraine. However, India was designated a priority foreign country in 1991.
The submissions by PhRMA and others "provide little reason to think India denies adequate and effective protection of intellectual property rights, or denies fair and equitable market access to companies in the US as far as the pharmaceutical industry is concerned," said DG Shah of Indian Pharmaceutical Alliance.
On the issue of India's compulsory licensing regime, James Love of non-profit organisation Knowledge Ecology International, said, USTR should have provided a fuller explanation of the circumstances that led to the compulsory licence in India. Bayer was charging R3.412 million per year for the drug, more than $69,000 per year at February 2012 exchange rates, and selling the drug to almost no cancer patients in India.
Professor Srividhya Ragavan (University of Oklahoma College of Law), Brook Baker (School of Law, Northeastern University) and Sean Flynn (American University, Washington College of Law) said that nothing has happened since the last Special 301 Report to justify a further downgrading of Indias status as Priority Foreign Country, adding that "USTR cannot use decisions that were considered and accounted for in the previous years to designate a country to a newer status".
America's major defence and civil aviation firms, Honeywell and Boeing, also came out strongly in support of India's IPR regulations. While Honeywell International said in its submission that India's IPR framework was one of the key enablers in the establishment of Honeywell's engineering and technology presence, Boeing contended that India's legal framework was adequate to protect IP with no known cases of violation.