Govt mulls USFDA-like checks to keep MNC drug makers on toes

Jan 29 2014, 08:35 IST
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Over the past few years, a number of Indian drug makers have been hauled up by the USFDA over issues relating to violation of good manufacturing practices. (Thinkstock) Over the past few years, a number of Indian drug makers have been hauled up by the USFDA over issues relating to violation of good manufacturing practices. (Thinkstock)
SummaryDrug Controller General to start system of sudden inspections of manufacturing facilities of pharma cos.

Concerned by increasing regulatory action against domestic drug makers in the United States and Europe, the government is planning to initiate a similar system of checks on pharma manufacturers, including multi-national firms operating out of India.

The Drug Controller General of India is set to start a system of sudden inspections of manufacturing facilities of pharma companies, including those of multi-national companies and will take stringent action against any violations.

“There has to be a level playing field. If foreign regulators can make surprise checks on Indian pharma companies, we can do the same for both domestic as well as foreign drug

makers,” said GN Singh, Drug Controller General of India (DCGI).

At present, teams from the DCGI and state drug control officers conduct checks but firms are usually notified in advance of such visits. In case of any violations, the facilities are given at least a 45 day window to comply with norms that can be increased on a case-by-case basis.

India pharma exports

The move comes soon after the US Food and Drug Administration (USFDA) banned Ranbaxy Laboratories's fourth unit at Toansa last Friday.

Although the DCGI is also set to inspect the facility to check for manufacturing violations, sources said there is increasing concern in the government over the regulatory action that Indian drug makers are facing abroad.

“Nearly 30 per cent of the generic medicines

consumed in the US is manufactured by Indian drug makers. This is not a new phenomena but this has been the same for the last 10 years,” pointed out a senior government official.

Over the past few years, a number of Indian drug makers have been hauled up by the USFDA over issues relating to violation of good manufacturing practices. Pharma firms including Wockhardt, Fresenius Kabi, RPG Life Sciences have got warning letters from

the USFDA earlier while others including Ranbaxy, Dr Reddy’s Labs, Sun Pharma, Cadila, Aurobindo Pharma and Glenmark

have faced action for non-compliance with various US regulations.

Also, the UK Medicines and Healthcare Products Regulatory Agency had

earlier issued a precautionary recall for sixteen medicines made by Wockhardt’s Waluj facility.

With an estimated size of over Rs 72,000 crore in 2013, the Indian pharmaceutical industry is one of the largest exporters of generic drugs in the world.

The United States is the top market for Indian pharma exports, accounting for 26 per cent of

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