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    Cipla API facility in Bengaluru gets EIR from USFDA

    Medical Dialogues BureauWritten by Medical Dialogues Bureau Published On 2019-09-23T09:45:33+05:30  |  Updated On 23 Sep 2019 4:15 AM GMT
    Cipla API facility in Bengaluru gets EIR from USFDA

    Cipla had earlier said that USFDA issued seven observations after conducting a routine 'CGMP inspection' at Cipla's API manufacturing facility in Virgonangar, Bengaluru.


    NEW DELHI: Cipla Ltd on Sunday announced the closure of inspection by the US health regulator at the company's API manufacturing facility in Bengaluru.


    "Following the inspection by the United States Food and Drug Administration (USFDA) at Company's API manufacturing facility in Virgonagar, Bengaluru, from July 15- 19, 2019, the company has received the Establishment Inspection Report (EIR), indicating closure of the inspection," the company said in a filing to the BSE.


    Read Also: Cipla arm, Novartis enter agreement for Ultibro Breezhaler to treat COPD


    The company had earlier said that USFDA issued seven observations after conducting a routine 'CGMP inspection' at Cipla's API manufacturing facility in Virgonangar, Bengaluru.


    Read Also: Cipla, Stempeutics ink licensing deal for Stempeucel-DFU to treat a diabetic foot ulcer

    API Bengaluru facility CGMP inspection Cipla Cipla CGMP inspection Cipla Virgonagar EIR Establishment Inspection Report pharma pharma company pharma news pharma news india US health regulator USFDA USFDA inspection USFDA observations Virgonangar 
    Source : PTI

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    Medical Dialogues Bureau
    Medical Dialogues Bureau

      Medical Dialogues Bureau consists of a team of passionate medical/scientific writers, led by doctors and healthcare researchers.  Our team efforts to bring you updated and timely news about the important happenings of the medical and healthcare sector. Our editorial team can be reached at editorial@medicaldialogues.in. Check out more about our bureau/team here

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