HomeNewsBusinessStocksHere’s what analysts feel about Dr Reddy’s Labs post US FDA observations

Here’s what analysts feel about Dr Reddy’s Labs post US FDA observations

Typically, the US drug regulator conveys its concerns on manufacturing practices through Form 483. Companies that receive its observations must respond in writing with a corrective action plan and implement it quickly

March 22, 2017 / 16:41 IST
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Representative image.
Representative image.

Moneycontrol News

Dr Reddy’s Laboratories was in focus on Tuesday after it received observations from the US Food and Drug Administration (FDA).

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The US Food and Drug Administration (FDA) issued these observations for its Duvvuda oncology formulation facility. The facility, called Unit-7, is located in Visakhapatnam Special Economic Zone (VSEZ). The site manufactures cytotoxic and hormonal injectables and is an important plant given Dr Reddy’s focus on complex generic filings.

The Unit-7 had received a warning letter in November 2015 for batch failures, a probable microbial contamination and certain lapses quality control procedures.