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    Cadila Healthcare Gujarat facility clears USFDA inspection

    Farhat NasimWritten by Farhat Nasim Published On 2019-12-22T09:30:17+05:30  |  Updated On 22 Dec 2019 9:30 AM IST

    "We hereby inform that the USFDA inspected the Company’s topical manufacturing facility located in Ahmedabad from 16th to 20th December 2019," Cadila said in a filing


    Ahmedabad: Pharma major, Cadila Healthcare recently informed the bourses that the company's topical manufacturing facility in Gujarat has cleared the US drug regulator's inspection.


    The US Food and Drug Administration (USFDA) inspected the topical manufacturing facility located in Ahmedabad from 16th to 20th December 2019.


    "We hereby inform that the USFDA inspected the Company’s topical manufacturing facility located in Ahmedabad from 16th to 20th December 2019," Cadila said in a BSE filing


    At the end of the inspection, no observation (483) is issued," the company added.


    Also Read: Zydus Cadila unveils affordable anti-diabetic drug Vildagliptin under brands Vinglyn, Vinglyn M


    Cadila Healthcare was founded in 1952 by Ramanbhai Patel, formerly a lecturer in the L.M. College of Pharmacy, and his business partner Indravadan Modi. It evolved over the next four decades into an established pharmaceutical company.


    Also Read: Zydus Cadila files NDA with DCGI for liver disease drug Saroglitazar Magnesium

    Cadilacadila gujarat facilityCadila Healthcareform 483pharmapharma copharma newspharma news indiatopical manufacturing unitUSFDAusfda 483USFDA inspection

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    Farhat Nasim
    Farhat Nasim

      Farhat Nasim joined Medical Dialogue an Editor for the Business Section in 2017. She Covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She is a graduate of St.Xavier’s College Ranchi. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751 To know about our editorial team click here

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