It is hereby notified that, as per the legal requirement stated in the National Medicines (Registration and Licensing of Medicine) Regulations, 2019 published on 14.10.2019 by gazette bearing No.2145/01, all manufacturers/importers are required to provide details of Authorized Regulatory Affairs Officer/s (name of the authorized officer, name of the company, NIC number, contact details etc.) in your respective organizations responsible for documents pertaining to registration of medicines, manufacturing licenses, technical matters, and other correspondence with the Authority to the NMRA on or before 17th of November 2020.

Access to the NMRA premises will only be given to such Authorized Officers after 17th of November.

(Date: 20 November 2020)