HomeNewsBusinessCompaniesRe-audit of Duvvada unit: Why an all clear holds importance for Dr Reddy’s

Re-audit of Duvvada unit: Why an all clear holds importance for Dr Reddy’s

A portion of complex abbreviated new drug applications is filed from this facility

October 24, 2018 / 16:55 IST
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Viswanath Pilla Moneycontrol News

Outcome of the crucial US Food & Drug Administration re-inspection of Dr Reddy's Laboratories injectable plant in Duvvada, Visakhapatnam, is keenly awaited by analysts as the unit is crucial to its future growth prospects in the US.

The company's Duvvada unit, known as FTO-VII, manufactures cytotoxic and hormonal injectables is under warning since November 2015, blocking any new approvals. Such a letter is issued when USFDA finds serious deviations from good manufacturing practices at a plant.

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The inspection which has begun on October 22 may take at least a week if not more. The drug regulator is generally more stringent while dealing with injectable plants, given the risks of contamination.

DRL declined to comment on the ongoing inspection. A company spokesperson told Moneycontrol that as a policy the management doesn't comment on regulatory inspections.