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U.S. FDA found four procedural issues at Piramal Pharma’s Indian plant; company vows cooperation and compliance.
The U.S. FDA issued a Form 483 with four observations during an inspection of Piramal Pharma’s Digwal plant in Telangana, India, from February 9 to 13, 2026.
The findings, related to procedural improvements rather than data integrity, are classified as Voluntary Action Indicated.
Piramal Pharma said it is preparing a response to submit within the required timeframe and reaffirmed its commitment to compliance and quality, pledging close cooperation with the FDA to address the issues.
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La FDA de EE.UU. encontró cuatro problemas de procedimiento en la planta india de Piramal Pharma; la compañía promete cooperación y cumplimiento.