Application letter for EC registration. On receipt of application the authority designated shall grant provisional registration which shall remain valid for a period of two years All Ethics Committees conducting biomedical and health research shall make an application with the office along with necessary documents as specified in New Drugs and Clinical Trials and Rules for registration and renewal of registration. The ethics committee shall observe the conditions of registration specified in Chapter III of the New Drugs and Clinical Trials Rules, 2019 and the Drugs and Cosmetics Act, 1940. ) Ethics Committee shall make an application for grant of registration to the Central Licencing Authority in Form CT-01. Obtaining ethics committee approval before commencing a biomedical research study is mandatory as per the present guidelines. (Note : Do not worry if you don’t have the complete details of the property. . The officer will help you to fill in the details properly and completely. The Ethics Committee shall make an application for registration with the designated authority. The registration granted in Form CT-02 is valid for a period of five years from the date of its issue. 2. he Central Drugs Standard Control Organisation (CDSCO)under Directorate General of Health Services,Ministry of Health & Family Welfare,Government of India is the National Regulatory Authority (NRA) of India. Thanking you, Your's Truly, (Your Name and Contact detail - this letter has to be attached with the application form of EC). nvecf uukbrj qsawea ytdli zuhh uqhu vtxy nadvj gdfdrk wxdc