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USFDA slaps 19 warning letters to Indian pharma firms in 2019; highest in 4 years

The USFDA's Office of Manufacturing Quality (OMQ) at the Centre for Drug Evaluation Research (CDER) evaluates compliance with cGMP for drugs based on inspection reports and evidence gathered by USFDA investigators

twitter-logoPB Jayakumar | December 30, 2019 | Updated 19:39 IST
USFDA slaps 19 warning letters to Indian pharma firms in 2019; highest in 4 years
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The Indian pharmaceutical companies have received 19 warning letters, out of the 41 (46 per cent) issued by the Office of Manufacturing Quality of the US Food and Drug Administration (USFDA) in 2019, the most in four years. This reversed the recent trend wherein Indian companies had been increasingly complying with the standards and resolving their manufacturing quality issues quickly that had cropped up over the last four-five years.

If the Indian drug manufacturers accounted for nearly 50 per cent of the current good manufacturing practices (cGMP)-related warning letters in 2015, it reduced to less than 30 per cent in 2016. This number further reduced to 24 per cent in 2017. In 2018, none of the top ten domestic firms were in the cGMP warning letter list, though many firms were struggling to get out of the trouble.

Out of 68 warning letters issued by the USFDA in 2018, 10 were related to India. In 2017, India's share of warning letters was 17 out of 79. According to a study by the Indian Pharmaceutical Alliance (IPA) and consultancy firm McKinsey, a couple of years ago, the number of FDA inspections in India declined from 272 in 2017 to 192 in 2015, but the share of plants receiving a clearance without adverse observations increased from 32 per cent to 51 per cent.

The USFDA's Office of Manufacturing Quality (OMQ) at the Centre for Drug Evaluation Research (CDER) evaluates compliance with cGMP for drugs based on inspection reports and evidence gathered by USFDA investigators. Erring firms are issued notices with Form-483 observations detailing the errors and are given time to respond and rectify the issues. Warning letters are issued if the firms still fail to comply with the norms after the repeated inspections. Most warning letters issued in 2019 were mainly based on inspections held a year ago and analysing the progress of remediation.

Most importantly, leading domestic firms such as Lupin, Aurobindo, Glenmark, Strides Arcolab, Zydus Cadila and more were slapped with warning letters in 2019. These included Mylan Laboratories' Unit 8 at Vizianagaram, Andhra Pradesh; Cadila Healthcare's unit at Moraiya, Ahmedabad; Torrent Pharmaceuticals's facility at Indrad, Gujarat; Glenmark Pharmaceuticals' unit at Solan, Himachal Pradesh; Lupin Limited's Unit 1 at Mandideep, Madhya Pradesh; Lantech Pharmaceuticals' active ingredient unit in Hyderabad; Emcure Pharma's Pune unit; CTX Lifesciences' unit at Surat, Gujarat; Indoco Remedies' unit at Vasco Da Gama, Goa; Strides Pharma Science's Puducherry unit; Aurobindo Pharma's Unit XI at Srikakulam, Andhra Pradesh; Rxhomeo's unit in Hyderabad; Glint Cosmetics's unit at Navi Mumbai; Centurion Laboratories's unit at Manjusar, Gujarat; B. Jain Pharmaceuticals's unit at Bhiwadi, Rajasthan; Jubilant Generics' unit at Uttaranchal; Hospira Healthcare's unit at Irungattukottai, Chennai; Anicare Pharmaceutical's unit in Navi Mumbai and Vipor Chemicals's Vadodara unit.

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