Define a clear timeline for Inspection of Manufacturing Sites of Medical Devices
Reform IDF334
DescriptionBefore: The inspection process for medical device manufacturing sites lacked a defined timeline, causing registration delays, increasing operational costs and uncertainty for manufacturers and investors.
After: A clear and standardized inspection timeline has been established, supported by technology-based tracking and optional third-party inspections, ensuring efficiency, transparency, and faster registration.
DepartmentDrug Regulatory Authority of Pakistan - DRAP
Jurisdiction / LocationFederal - Entire Pakistan
SectorPharmaceuticals and Healthcare
Start Date24-06-2025
Target Deadline30-06-2025
Date Enacted
Implementation StatusCompleted
Progress 100%
CCORR DirectionSimplify
Cost Savings PKR (Mil.)270
EvidenceView Evidence