To all representatives of companies
With effected from 1st January 2017,
Those who submit applications for registration of foreign manufacturing sites and product registration dossiers for Medicines, Medical Devices and Borderline Products should submit two (2) soft copies separately in an un-editable pdf format (2 CDs) with the applications.
(Such applications will not be accepted without the CDs from 1st January 2017)
Dr. Kamal Jayasinghe,
Chief Executive Officer,
National Medicines Regulatory Authority.