
Metina is a pharmaceutical consulting firm with expertise in submissions and approvals for the USA, EU and emerging markets, and in filing and approval of ANDAs, NDAs, NCEs and branded generic products worldwide. The company offers end-to-end regulatory and business development activities including strategy development, dossier due diligence, in-license/out-license of dossiers, submission management to health authorities and product market launch, along with consultancy for EU GMP approvals and API QP audits of manufacturing sites in India and worldwide.

No hay comentarios disponibles.
Deja tu valoración & comentario