Clinical investigation team Briefly describe the administrative structure of the clin ...

General Central Drugs Standard Control Organization, Ministry of Health and Family We ...

7.2 Bio-compatibility: (i) The dossier should contain a list of all materials in dire ...

Application for grant of permission to conduct clinical investigation (1) An applicat ...

(iv) the person holding registration certificate shall maintain records of tests for ...

The application under sub-rule (1) shall be made through an identified online portal ...

19M. Cancellation or suspension of registration.― (1) The State Licensing Authority ...

Product standards for medical device (1) The medical device shall conform to the stan ...