Metina is a Regulatory Affairs consulting firm having expertise in submissions and approvals for USA, EU and Emerging Markets and expertise in filing & approval of ANDA, NDA, NCE as well as Branded Generic Products across the globe. Metina currently offers consultancy services to Pharmaceutical Industry and covers end to end regulatory and business development activity covering strategy development, due diligence of dossier, in -license/out-license of dossiers, Submission Management to Health Authorities, GMP audits Personal meeting with Health Authorities and product market launch.
Metina's team is comprised of regulatory / clinical professionals based in Mumbai, India. The academic qualification of the members varies from Clinical Doctors, Toxicologists, Doctorate in Chemistry and Pharmaceuticals, Master of Pharmacy and Bachelor of Pharmacy. These members are well versed with the latest international regulatory standards / guidelines and have industry experience in the range of 3-16 years.
Metina has regulatory / business associates across EU, USA, Asia, Africa (Including MENA), GCC, Latin America and Russia / CIS region. These associates help manage regulatory submissions with respective health authorities and bring marketing authorisation approvals for the company.
"To support Pharmaceutical Companies to build, grow and expand their international presence by managing highest quality regulatory submissions with speedy approvals/entry to markets at competitive costs."