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Centre approves plan to strengthen drug regulatory system at Rs.1750 cr

Our Bureau, Hyderabad
Friday, August 14, 2015, 08:00 Hrs  [IST]

The Central government has approved a proposal to spend Rs. 1750 crore for the next 3 years to strengthen the drug regulatory system in the country. In this regard, the Cabinet Committee on Economic Affairs, chaired by the Prime Minister Narendra Modi, has approved the proposal for strengthening the drug regulatory system both at the central and the state levels.

According to a report released by the government, the strengthening or up-gradation of the drug regulatory system will be spread over a period of three years and with a total of Rs.1750 crore. Of which, Rs.900 crore will be spent on strengthening central structures and Rs.850 crore will be made available to the state governments, after signing a memorandum of understanding.

The up-gradation will include provision of additional equipment and manpower in existing drug testing laboratories; setting up of new laboratories for testing drugs, medical devices and cosmetics; making mobile drug testing laboratories available; creation of additional manpower for regulatory structures, including for new and emerging areas such as stem cell, regenerative medicine, biologicals and medical devices in addition to drugs. The upgradation will also introduce organisation wide e-governance and information technology enabled/online services, and setting up a training academy for regulatory and drug testing officials, of both the central and state governments.

Assistance will be provided to the states for strengthening their drug regulatory structures. The measure will help enhance quality, safety and efficacy of drugs and other medical products manufactured in the country, and thereby help mitigate the disease burden as also increase export of pharmaceutical products from India. Besides, it will also help trigger growth of the domestic medical devices sector.

According to regulatory sources, implementation of the said scheme will facilitate domestic manufacture of quality medical products and help establish a robust industry in the field of medical devices, biological and other areas. The common training programmes for regulatory and laboratory staff will also help in evolving uniform practices throughout the country. “Regular training to drug administrative staff and drug inspectors is very important. We have been demanding the government to strengthen the human resources and laboratory infrastructure. Sending drug inspectors to overseas will help gain knowledge about regulatory systems of other countries and implement the best practices to strengthen our own system,” says Ravi Uday Bhaskar, secretary general, AIDCOC.


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