Eliminate Export-permit for medical device and adopt a risk based approach
Reform IDF601
DescriptionBefore: Under the Medical Devices Rules, 201718The Export Permit for medical devices is a formal authorization issued by the Medical Device Board (MDB) of the Drug Regulatory Authority of Pakistan (DRAP). A single application is required for the export of one or more medical devices manufactured by the same establishment, and a single permit is issued accordingly. Mandatory export permits, documentation requirements, and regulatory approvals increase compliance costs and may delay the export of medical devices to international markets.
DepartmentDrug Regulatory Authority of Pakistan - DRAP
Jurisdiction / LocationFederal - Entire Pakistan
SectorAll Sectors
Start Date04-02-2026
Target Deadline
Date Enacted
Implementation StatusIn Progress
Progress 0%
CCORR Direction
Cost Savings PKR (Mil.)
Evidence