Cadila Healthcare gets EIR report from USFDA

Published On 2016-01-11 03:50 GMT   |   Update On 2016-01-11 03:50 GMT

New Delhi: Drug firm Cadila Healthcare said it has received Establishment Inspection Report (EIR) for Baddi manufacturing plant from the US health regulator after successful inspection closure.The company's "manufacturing plant at Baddi, Himachal Pradesh, has successfully obtained the Establishment Inspection Report from the United States Food and Drug Administration (USFDA)", Cadila...

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New Delhi: Drug firm Cadila Healthcare said it has received Establishment Inspection Report (EIR) for Baddi manufacturing plant from the US health regulator after successful inspection closure.

The company's "manufacturing plant at Baddi, Himachal Pradesh, has successfully obtained the Establishment Inspection Report from the United States Food and Drug Administration (USFDA)", Cadila Healthcare said in a BSE filing.

This will now pave the way for further approval of products from this site, it added. The company makes formulations at its Baddi manufacturing facility.

Establishment Inspection Report is given to an establishment after the completion of the inspection by the FDA.
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