Last Updated on June 13, 2021 by The Health Master
Import of Drugs
Government of India, Ministry of Health and Family Welfare has published a Gazette Notification GSR no. 604 (E) dated 24.08.2001 amending the various provisions of the Drugs & Cosmetics Rules, thereby introducing a new provision for the registration of the manufacturing premises of foreign drug manufacturer and the individual drugs prior to their import into the country.
The notification has also introduced few other provisions viz. enhanced import licence fees, increased validity period of licence, deletion of exemption from requirement of import licence for bulk drugs for actual users, requirement of minimum 60% of retained shelf life for imported drugs and provisions for import of small quantities of new drugs by Govt. hospitals for treatment of their own patients etc.
Import and registration
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Import of drugs for personal use
Small quantities of drugs, the imports of which is otherwise prohibited under Section 10 of the Act, may be imported for personal use under Form-12A, subject to the conditions. For more details and to download Form 12, click below