Simplify the process of Medical Device Manufacturing License
Reform IDF333
DescriptionBefore: The medical device manufacturing license process was lengthy and inefficient, delayed market entry and disrupted production.
After: The licensing process has been streamlined through reduced documentation, defined timelines, and an online application system, ensuring faster approvals and smoother market entry.
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 DirectionSimplify & Digitize
Cost Savings PKR (Mil.)1618
EvidenceView Evidence