Drug Approval

Piramal Pharma completes USFDA inspection of Aurora facility with Zero Form-483 observations

The USFDA conducted a general GMP (Good Manufacturing Practices) Inspection of Piramal Pharma Limited's facility at Aurora, Canada from 26th May 2025 to 30th May, 2025.

The inspection was completed successfully with Zero Form - 483 observations and No Action Indicated (NAI) designation.

The company remains committed to maintain the highest standards of compliance.

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