Auro Laboratories Limited submits that the Company has received a "Certification of Substances Department" from the European Directorate for the Quality of Medicines & Healthcare ("EDQM") ....
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Auro Laboratories Limited has received an Attestation of Inspection from the European Directorate for the Quality of Medicines & Healthcare (EDQM) for its manufacturing facility at MIDC Tarapur, Maharashtra. The certification confirms compliance with EU Good Manufacturing Practice (GMP) requirements for Metformin Hydrochloride (CEP Dossier No. CEP 2005-123). The inspection reference number is INSP 2012-002-P05. This is a regulatory certification that validates the quality standards of the company's pharmaceutical manufacturing facility.
This GMP certification from EDQM enables Auro Laboratories to continue supplying Metformin Hydrochloride to European markets. It enhances the company's credibility as a quality-certified pharmaceutical ingredient manufacturer and removes a potential regulatory barrier for EU exports.