News about "EUGMP"

US FDA Clears Anuh Pharma Facility with No Form 483 Observations

US FDA Clears Anuh Pharma Facility with No Form 483 Observations

The Tarapur facility of Anuh Pharma is already an EUGMP/ WHO pre-qualified approved manufacturing facility with nine API’s blocks and two intermediate block with total capacity of 2400 MTPA.

EUGMP | 11/02/2026 | By News Bureau 158


 

 

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