A series of refresher training workshops brought together medical device stakeholders, including importers and manufacturers, to review the enhanced features of the MDMC Licensing and Product Registration Portal launched on 21st July 2025. The sessions aimed to familiarise users with practical steps to improve submission quality and navigation of the updated portal.
Trainers placed special emphasis on the PLV and PRV modules so participants could better understand module-specific requirements and avoid common errors. Hands-on demonstrations and scenario-based practice helped attendees apply the portal’s new validation checks and data entry formats.
Organised in collaboration with HDAP, the workshops reached stakeholders across Islamabad, Peshawar, Lahore and Karachi, creating a forum where industry representatives and regulators could reflect on shared challenges and exchange practical insights. Discussions reinforced a collective commitment to strengthening portal processes related to registration, licensing and PRVs.
Officials and participants expect these refresher sessions to reduce application errors from stakeholders and further shorten the time required for decision making, improving the overall efficiency of medical device registration and licensing through the MDMC portal.
