Indian Girls Become the Guinea Pigs for Western Cos

By siliconindia   |   Friday, 18 November 2011, 23:53 IST   |    37 Comments
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While it is said that the crucial trials were carried out following appropriate guidelines, the report says the lack of oversight have resulted in a situation where poor and often illiterate individuals, picked from the tribal areas or city slums are used for the critical trials without obtaining proper informed consent which means they have apparently agreed to the trials without fully understanding what they are signing up for. At the shadow of this inhuman practice of drug trials on humans, a new industry has been spawned making significant profits by providing participants for these studies.

An investigation by 'The Independent' in the Indian states of Madhya Pradesh, Andhra Pradesh, as well as in Delhi and in London shows that hundreds of Indian tribal girls were recruited without proper parental consent for an immunization study sponsored by the Bill and Melinda Gates Foundation, shockingly just on the node of the government hostel's warden. Several girls have reportedly been killed and then the controversial study was stopped by the federal authorities. The investigation also found the use by drug companies of survivors of the Bhopal tragedy, world's worst poisonous gas disaster, as 'guinea pigs' in at least 11 trials without proper informed consent. In another shocking finding, many cases of drug trials were reported at a government hospital in Indore of which 81 cases of adverse effects were reported.

India is just one of those many developing countries being exploited for its large, ignorant and illiterate tribals by the Western pharmaceutical giants who spent over 40 billion pounds last year on research and development. It's said that over 120,000 trials are taking place in 178 countries and the companies can reportedly reduce up to 60 percent of their spending on research through outsourcing the works to these third world countries. The article also reveals that a quarter of all clinical data submitted to European drug regulators for approval are obtained from trials in low- and middle-income countries.