Under the drugs and cosmetics act. CDSCO is responsible for approval of new drugs, conduct of clinical trials , laying down the standards for drugs control over the quality of imported drugs in the country and coordination of the activities.
CDSCO is the National Regulatory Authority for Indian pharmaceuticals and medical devices under the Directorate General of Health Services, Ministry of Health and Family Welfare in India.It is the responsibility of CDSCO for approving new drugs and conduct of clinical trials in India under the Drugs and Cosmetics Act, 1940 (“Act”) and Drugs and Cosmetics Rules, 1945.
(1) Cosmetics
(2) DCC-DTAB
(3) BA/BE
(4) Medical Devices and Diagnostics
(1) Gather the required documents
(2) File and submit the cdsco online application
(3) Wait for the cdsco's assessment of the application
(4) Getting the registration number for cosmetics import
(1) Power attorney.
(2) Undertaking and declarations.
(3) Ingradient Details.
(4) Product label.
(5) License and certification
(6) Licensing fee
(7) Testing Report
(1) What is CDSCO Registration?
(2) Who approved medical device in india?
(3) How much time is required for the development of new drug?
(4) Is CDSCO Statutory?