Regulatory affairs, GMP and GCP

Regulatory affairs in pharma industry is the area which involves compliance of regulatory principles regarding quality, safety and efficacy of drugs. It involves development plans, supervising, reviewing and assembling and submission management. Regulation involves extensive evaluation of a particular drug or drug product to ensure protection of patient, registration of drug, marketing authorization, import and distribution and pharmacovigilance.

Conference on Regulatory Affairs | GMP Conferences | GCP Conferences


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