Duty D11-XMJ, published by Directorate General of Health Services, Ministry of Health and Family Welfare [D11-XMJ]
As at 6 September 2026. In force from 8 October 2010.
Addressee: Every manufacturer.
Required: Obtain a licence before undertaking the manufacture of drugs; apply in Form 25, fee five hundred rupees.
Period: Before the activity begins; licence valid three years.
Form: Form 25.
Source: Section 6, Clinical Establishments (Registration and Regulation) Act, 2010 [S25-JJS].
Penalty provision: Section 61, Clinical Establishments (Registration and Regulation) Act, 2010 [S25-M9J].
Published by: Directorate General of Health Services, Ministry of Health and Family Welfare.
In force: from 8 October 2010.