The number of such deaths in 2011 was 438 while in 2010 it was 668.
In 2011, 16 deaths out of a total of 438 were due to clinical trials and in 2010 there were 22 such serious adverse events of deaths (SAE) due to drug trials. In a written reply to a question in the Lok Sabha, Health and Family Welfare Minister Ghulam Nabi Azad today said the cases of 2012 are "under examination" as all such deaths are investigated to arrive at a causal relationship.
Azad said of the 480 applications received for conducting clinical trials of new drugs/vaccines on human beings in the country in 2012, 253 were granted permission for conducting the same, against 283 granted in 2011 out of 306 applications received. As many as 529 permissions for new drug trials were granted against 546 applications in 2010.
The Minister said government has taken a number of steps to strengthen the approval procedures and monitoring mechanism for clinical trials and to ensure safety, rights and well-being of trial subjects, which includes the amendments notified in the Drugs and Cosmetics Rules, 1945.
So far, there were no procedures in place to ensure accountability of this hitherto unregulated sector which is worth USD 500 million in India.
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