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ProPharma Group

ProPharma Group works on projects that may cover the complete life cycle of a product from (early) development up to post approval maintenance. The offer includes CMC (Chemistry, Manufacturing & Controls) regulatory leadership and strategy required to achieve regulatory approvals.

We provide strategic advice related to (clinical) regulatory affairs, draft and review regulatory documents and help to define regulatory strategy for drug development projects. ProPharma Group is your regulatory expert in clinical product development teams, for short- and long-term projects.

ProPharma Group is an international, independent, single-source provider of comprehensive compliance services that span the entire lifecycle of pharmaceuticals, biologics, and medical devices. ProPharma Group has more than 1,200 colleagues worldwide providing an unmatched variety of compliance related services including life science consulting, medical information, pharmacovigilance, and regulatory affairs

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