Piramal Pharma Limited has announced the successful closure of a US Food and Drug Administration (US FDA) inspection at its manufacturing facility in Sellersville, Pennsylvania, USA.
The company informed the stock exchanges that the US FDA has issued an Establishment Inspection Report (EIR), indicating that the regulatory inspection at the facility has been successfully concluded.
The company stated that the US FDA has issued an Establishment Inspection Report (EIR) for its Sellersville manufacturing facility.
The issuance of the EIR signifies the successful completion and closure of the inspection conducted by the US regulator. Piramal Pharma had previously informed the exchanges about the inspection on May 10, 2026.
The successful closure of the inspection represents an important regulatory milestone for the Sellersville facility.
Manufacturing facilities supplying pharmaceutical products to the US market are subject to periodic inspections by the US FDA to assess compliance with current Good Manufacturing Practices (cGMP) and applicable quality standards.
Piramal Pharma operates a global network of manufacturing facilities serving customers across multiple regulated markets.
The successful completion of the US FDA inspection supports the continued operations of the Sellersville facility and reinforces the company's focus on maintaining regulatory compliance and quality standards across its manufacturing network.
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As of 09 July 2026, at 2:25 PM, Piramal Pharma share price was trading at ₹172.59 per share, reflecting a surge of 2.66% from the previous trading session.
Piramal Pharma has successfully concluded the US FDA inspection of its Sellersville, USA manufacturing facility after receiving an Establishment Inspection Report (EIR). The regulatory milestone reflects the successful closure of the inspection and supports the company's ongoing manufacturing operations in regulated markets.
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Published on: Jul 9, 2026, 4:04 PM IST
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