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Law
1. To make patent laws imposed on life saving drugs lighter. The price of these drugs must
be fixed according to the per capita income of the country. The ever greening has become
serious issue by which pharmaceuticals make some minor change in their patented
medicine and try to re patent it to maintain its monopoly and to raise the price claiming a
new innovation. When Novartis tried to raise the price claiming a new patent from 2500
USD to 70000USD, this kind of law was made in India.
The Indian Union Minister of Commerce and Industry, Shri Kamal Nath in support of the
new Indian patent law said:
The price of medicines will not shoot up due to patents, because of these strong safeguards,
check and balance. There are comprehensive provisions in the amended Act to deal with
issues concerning the price and availability of medicines. These include provisions for
compulsory licensing to ensure availability of products at reasonable price; parallel import
of products; acquisition of patent rights by the government; revocation of patents in the
public interest; and provisions to deal with emergency situations.
2. Putting extra patent fees on drugs and medicines which are not directly related with
human life and death like anti-aging creams. These high prices for luxury products will be
helpful for making up the cost of low price in developing countries.
5. Less bureaucracy in patenting procedure meaning the procedures must be simple but
law will be strict.
6. Making patent laws regarding GOM very strict. They must be given after proper testing
procedure on non-human species. The patentee must bear all the responsibility if any
disaster happens. If there is any violation of health issues after patent has been granted,
victims must be given proper compensation by the patentee pharmaceutical industry. Also
the patent will be canceled.
7. Although created under the auspices of free trade, TRIPS, was the product of intense
lobbying by the world’s largest and most powerful pharmaceutical companies like Merck,
Pfizer, GlaxoSmithKline, and Eli Lilly and of intense political pressure by the world’s largest
and most powerful countries (U.S., Europe, and Japan). To put it in perspective, the financial
power of these pharmaceutical companies relative to developing countries is reflected by
their market capitalization, which is collectively greater than the economies of Mexico and
India and twice the gross national product of sub-Saharan Africa. This financial power has
been converted into tremendous political influence both nationally and internationally. The
Pharmaceutical Research and Manufacturers of America (PhRMA), the most powerful
pharmaceutical industry lobby in the U.S., was a driving force in getting TRIPS adopted and
then played a leading role in encouraging the Bush Administration to use bilateral
negotiations and unilateral economic sanctions against countries that PhRMA believes offer
inadequate patent protection. Granting patent protection to pharmaceutical companies
creates pharmaceutical monopolies, which in turn translates into higher drug prices based
on the companies’ ability to limit access to these drugs. To reduce drug prices, the WTO
should consider a major reformation of TRIPS, in order to create a competitive market for
generic drugs in developing countries. If any country uses its pharmaceutical lifesaving and
crucial drugs to influence any political or military negotiations, that industry must be
stripped off its patent.
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