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    Dr Reddy's Labs gets EIR from USFDA for Srikakulam unit

    Written by Ruby Khatun Khatun   |  
    Dr Reddys Labs gets EIR from USFDA for Srikakulam unit

    New Delhi: Dr Reddy's Laboratories said it has received an Establishment Inspection Report (EIR) from the US health regulator for its Srikakulam facility in Andhra Pradesh.


    The Srikakulam unit manufactures active pharmaceutical ingredients (APIs).


    The EIR from the United States Food and Drug Administration (USFDA) indicates closure of the audit of the plant, Dr Reddy's Labs said in a BSE filing.


    In an earlier filing on June 2, 2018, the company had said that the audit of the Srikakulam plant (SEZ) by USFDA had been completed with no observations.

    active pharmaceutical ingredientsAndhra PradeshAPIsDr ReddyDr Reddy'sDr Reddy's LaboratoriesDr Reddy's LabsEIREstablishment Inspection Reportno observationsSrikakulam unitUnited States Food and Drug AdministrationUSFDA
    Source : PTI

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    Ruby Khatun Khatun
    Ruby Khatun Khatun
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