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To all representatives of Importers

NOTICE

 


To all representatives of Importers

With effect from 15th June 2017,

those who submit applications for registration of medicinal products and medical devices should submit the following supporting documents from the manufacturer.

 

  1. CIF price of the product
  2. Regional price of the product
  3. Price of the product in country of origin

 

 

Chairman / Chief Executive Officer,

National Medicines Regulatory Authority.

 

30.05.2017