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The Economic Times
No observations by US FDA during plant inspection: DRL
Dr. Reddy's Laboratories announced that the U.S. Food & Drug Administration (FDA) completed a routine Good Manufacturing Practice (GMP) inspection of its integrated product development organization in Bachupally, Hyderabad, with zero observations. The company shared this update in a stock exchange filing on Friday, highlighting compliance with regulatory standards.
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Fri, Sep 20, 2024
Business Standard
DRL's Andhra Pradesh facility gets 3 observations from USFDA
Dr Reddy's Laboratories said that the US drug regulator has issued Form 483, with three observations after inspecting its Andhra Pradesh manufacturing facility.
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Sat, Aug 24, 2024