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Health ministry to amend D&C Act to strengthen rules for clinical trials, medical devices

Ramesh Shankar, MumbaiWednesday, December 29, 2010, 08:00 Hrs  [IST]

The Union health ministry has started the process of further amendments to the Drugs and Cosmetics Act to streamline the rules in the clinical trials and medical devices segment in the country. Redrafting of the D&C Act in this regard is in an advanced stage and the ministry proposes to introduce the amendments in the next session of Parliament for its final nod, it is learnt.

Sources in the health ministry, who are involved in the redrafting process, said that the entire process is being done by the ministry according to the recommendation of the Mashelkar Committee, which had recommended an overhaul in the Act to make it more effective. Apart from other administrative changes like the creation of a Central Drug Authority (CDA), the Mashelkar committee had recommended to the government to make the punishment for manufacturing and marketing of spurious drugs more stringent.

The Union health ministry had already amended the D &C Act to make punishment part more stringent. The Drugs and Cosmetics (Amendment) Bill, better known as Spurious Drugs Act, was passed by Parliament in October 2008 and it received President's assent in December same year. The union health ministry on August 10, 2009 had notified the Drugs Act Amendment Bill, enhancing the punishment to 10 years imprisonment and a fine of Rs. 10 lakh for production and sale of spurious drugs. Under the new amendment in the Act, production and sale of spurious drug was made a non-bailable offence.

After making the punishment part of the Act more stringent, now the ministry wanted to bring the segments like clinical trials and medical devices under its ambit for further streamlining the regulations. The development is part of a series of measures being undertaken by ministry to strengthen regulatory monitoring of clinical trials and medical devices in the country.

Regulation of clinical trials has become important as cases of deaths among patient groups undergoing drug under trials have become more recently which sometimes make an outcry form the NGOs and public. According to official records, 462 deaths of clinical trial subjects were reported during the year (till June 2010). The number of deaths were 637 in 2009, 288 in 2008 and 132 in 2007.

 
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