Simplify & Digitize current Goods Manufacturing Practices (cGMP) certificate
Reform ID		F258
Description		The issuance and renewal of GMP certificates at DRAP involve manual submissions, physical inspections, paper-based documentation, and multiple approval stages, resulting in delays and increased compliance burden for pharmaceutical manufacturers. Despite DRAP’s ongoing cGMP inspection and risk-based compliance framework, the absence of a fully digitized end-to-end certification process limits transparency, real-time tracking, and timely issuance of certificate.
Department		Drug Regulatory Authority of Pakistan - DRAP
Jurisdiction / Location		Federal - Entire Pakistan
Sector		Pharmaceuticals and Healthcare
Start Date		18-08-2025
Target Deadline		18-09-2025
Date Enacted		17-04-2025
Implementation Status		Completed
Progress		100%
CCORR Direction		Simplify & Digitize
Cost Savings PKR (Mil.)
Evidence		View Evidence