All authorized representatives of companies

All authorized agents for Medical Devices are hereby informed that National Medicines Regulatory Authority ( NMRA ) would entertain applications for registration of COVID 19 Rapid Antigen Test Kits on priority and expedited review basis . Listing by the WHO will be an added qualification for such review .

You are hereby advised to submit your application through e - NMRA system.

(Date: 26 October 2020)

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