Maintenance of records.― (1) The manufacturer or, as the case may be, importer shal ...

INFORMED CONSENT FORM 1. Checklist for clinical investigation Subject's informed cons ...

(f) Undertaking signed stating that the manufacturing site is in compliance with the ...

Explanation : For the purpose of these rules, substances used for in vitro diagnosis ...

Duties of Medical Device Officer Subject to the instructions of the Central Licensing ...

Under the Drugs and Cosmetics Act, CDSCO is responsible for approval of New Drugs, Co ...

The Drugs & Cosmetics Act, 1940 and rules 1945 have entrusted various responsibilitie ...

Under the Drugs and Cosmetics Act, CDSCO is responsible for approval of New Drugs, Co ...