The Medical Devices Regulatory Division of the NMRA has revised the Consolidated Dossier Submission Checklist for New Product Registration (F-MDR-035). The revised format can be obtained from the “Application Forms” tab under the Medical Devices Regulatory Division on the NMRA website.

Accordingly,all Market Authorization Holders are advised to submit consolidated dossiers in compliance with the revised checklist with effect from 02nd June 2026.

Chief Executive Officer

National medicines Regulatory Authority

‍