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Granules India to tighten oversight after US FDA warning, exec says

Author: admin_zeelivenews

Published: 09-04-2026, 9:57 AM
Granules India to tighten oversight after US FDA warning, exec says
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Last year, the US Food and Drug Administration flagged violations in good manufacturing practices, equipment ‌cleaning and contamination controls at Granules India’s plant in Telangana.

Last year, the US Food and Drug Administration flagged violations in good manufacturing practices, equipment ‌cleaning and contamination controls at Granules India’s plant in Telangana.
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BHARATHIKRISHNA

Granules India is increasing oversight at its manufacturing facilities and digitising documents after the ​US drug regulator flagged violations, including issues with record-keeping and contamination ‌control practices, at its largest plant, a ​top executive said.

The company, which is globally one ⁠of the largest paracetamol makers and a major player in the active pharmaceutical ingredients market, derives a bulk of its revenue from ‌the US.

Last year, the Food and Drug Administration flagged violations in good manufacturing practices, equipment ‌cleaning and contamination controls at the plant in ‌the ⁠southern Indian state of Telangana. The firm failed to ⁠establish and follow adequate written procedures for cleaning and maintenance of equipment, the FDA had said, adding that a large amount of ​torn data records were found ‌in 15 plastic waste bags.

While the warning did not halt production, it could temporarily affect FDA approval of new products manufactured at the site.

Granules has 10 ‌manufacturing plants, of which seven are in India, two ​in the US and one in Europe.

The drugmaker will move its operations logbooks, ⁠batch manufacturing records and badge cards online over the next few months to reduce data-related regulatory risks, its executive director, ‌Priyanka Chigurupati, told Reuters in an interview last month.

“We expect the FDA to come anytime,” Chigurupati said.

The company raised the frequency of so-called gemba walks, where managers observe manufacturing practices to identify bottlenecks, as part of its standard operating procedure at the facility.

“So whenever there’s ‌an issue, we stop and don’t move forward,” she said, adding ​that doing so will avoid issues with product quality. The firm will focus on implementing automation ⁠of data collection and tightening controls across facilities, and has set ⁠aside a ‘certain amount’ of capital expenditure, she said, without giving further details.

“We hadn’t thought about it (automation ‌and controls) earlier, but now we are, and it’s high time we did, so we’re really adapting ​and adopting those practices,” Chigurupati said.

Published on April 9, 2026

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