Automate Medical Device Registration & Enlistment process
Reform IDF332
DescriptionBefore: The medical device registration process was manual, lengthy, and uniform across all risk categories, resulting in administrative delays that can extend beyond two years.
After: A fully automated digital registration system has been implemented with defined timelines and a clock-stop feature that streamlines approvals, reduces delays, and ensures risk-based efficiency in medical device registration.
DepartmentDrug Regulatory Authority of Pakistan - DRAP
Jurisdiction / LocationFederal - Entire Pakistan
SectorPharmaceuticals and Healthcare
Start Date24-06-2025
Target Deadline30-06-2025
Date Enacted18-07-2025
Implementation StatusCompleted
Progress 100%
CCORR DirectionDigitize
Cost Savings PKR (Mil.)9400
EvidenceView Evidence