Piramal Pharma Business Update
Piramal Pharma reported that the US FDA issued a Form-483 with 7 observations following a GMP inspection of its Morpeth, UK facility.
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Piramal Pharma reported that the US FDA issued a Form-483 with 7 observations following a GMP inspection of its Morpeth, UK facility.
Piramal Pharma Limited released its Sustainability Report for FY2025-26, detailing the company's ESG performance across key pillars, including business resilience and operational sustainability.
Piramal Pharma has resumed operations at its Ahmedabad facility following the recent temporary suspension due to heavy rainfall. Operations are substantially restored with no material financial impact.
Piramal Pharma filed its BRSR for FY 2025-26, detailing operations, employees, and subsidiaries. The report is a routine compliance disclosure with no new financial or operational event.
Piramal Pharma received permanent revocation of closure directions for its Dahej site from GPCB. Operations continue normally, ensuring sustained manufacturing stability and environmental compliance.
Piramal Pharma received an Establishment Inspection Report from the US FDA for its Telangana facility. The inspection is successfully closed, ensuring regulatory compliance and operational continuity.
US FDA concluded inspection of Piramal Pharma's Sellersville facility with three observations. Inspectors recommended VAI classification, with no findings relating to data integrity.