The MDMC Portal refresher training brought together medical device importers, manufacturers and regulators to explore the enhanced features of the Licensing and Product Registration system launched on 21 July 2025. Participants reviewed recent updates to help align submission practices with the portal’s improved workflows and data requirements.
Trainers placed special emphasis on the PLV and PRV modules, demonstrating practical steps to reduce submission errors and ensuring stakeholders understand new validation checks. The sessions were organised in collaboration with HDAP and held across Islamabad, Peshawar, Lahore and Karachi to maximise industry reach.
Across each city, industry representatives and regulatory officials reflected on shared challenges, exchanged practical insights and reaffirmed a collective commitment to strengthen MDMC Portal processes related to registration, licensing and PRVs. The hands-on format allowed attendees to test common scenarios and clarify procedural questions with portal specialists.
Organisers expect the initiative to cut down application mistakes by stakeholders and shorten decision timelines, delivering more predictable outcomes for device approvals and licenses. For Pakistan’s medical device sector, the training aims to improve compliance and speed access to essential equipment by making the MDMC Portal easier and more reliable to use.
