Why India?   Clinical Research Industry      Europe      Asia      Latin America      United States   Clinical Trials   Clinical Data Management   Central Reference Lab     WHY INDIA - FAQ'S   10) What is the regulatory process in india?   The regulatory process is as below:     Please Note : DCGI: Drug Controller General of India DGFT: Directorate General of Foreign Trade GEAC: Genetic Engineering Approval Committee ICMR: Indian Council of Medical Research AERB: Atomic Energy Regulatory Board

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