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Metina is a pharmaceutical and bio-pharmaceutical consulting organization engaged in Gmp and regulatory services across the globe. Metina is expertised in submissions & approvals for USA, EU & emerging markets and expertise in filing & approval of ANDA, NDA, NCE, API GP audits as well as branded generic products. Metina offers consultancy services for regulatory & business development activity covering strategy development, due diligence of dossier, in-license/out-license of dossiers, submission management to ha, query response and approval, product market launch and EU GMP approvals. We consult for API and formulation for USA, EU, who PGP and emerging markets as well.