The IPA has initiated discussions with the American regulator to identify common problems
The pharmaceutical industry has been the subject of increased scrutiny by regulatory bodies worldwide and in the recent past, Indian pharma sector too has witnessed more scrutiny. The US FDA (Food and Drug Administration) is one regulator that requires the highest standards of safety and quality and even as an increasing number of Indian companies are attracted to and have a presence in the U.S. market, this also means that the numbers of inspections and defaults are rising.
D. G. Shah, Secretary General, Indian Pharmaceutical Alliance, said that Indian companies accounted for 12 per cent of the warning letters issued by US FDA. “After all, USA accounts for 30 per cent of India’s pharmaceutical exports of $ 3 billion and this is growing at 18-20 per cent per annum.”
In an interaction with The Hindu, Glenn Saldanha, Chairman & Managing Director Glenmark Pharma said the US FDA was unbiased and “is very rational and consistent in how it approaches things across the globe. As India is exporting a lot more to the U.S. now it is risk-based automatically, the vigilance has increased because of the sheer amount of products that we sell to the U.S.”
For Indian companies, 40 per cent or more have been inadvertent offences. While there are signs that the US FDA has become stringent, it is generally felt very strongly that domestic industry must get its act together particularly in compliance systems and must invest more in processes.
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