PharmaMatch specializes in API sourcing and intermediates for the regulated markets from companies around the world. We ensure our clients are matched with the right partner based on quality, price and regular supply. We can also provide third party audits or pre-audits for our clients to ensure the facilities are up to standard.
PharmaMatch has helped numerous manufacturing facilities achieve their EU-approval. Providing complete support to meet the cGMP requirements, we start with pre-auditing the facility which simulates an actual EU audit. Through our findings, we guide CAPA (Corrective And Preventive Actions) and help implement any changes required. We can also trigger the EU audit, ensure documentation is complete and help answer queries from the authorities.
With our forte in understanding the regulatory framework in every region, PharmaMatch has helped companies register their dossiers successfully around the world. We assist our partners in dossier compilation and updating of dossiers. Our regulatory team can also convert CTD dossiers to EuCTD and ACTD formats.