**Pakistan Advances Medical Device Digitization and Regulatory Reforms, Says Health Minister**
Pakistan’s Ministry of Health is accelerating the digitization of the country’s medical device regulatory system, a move expected to enhance transparency, efficiency, and quality assurance. Federal Health Minister Mustafa Kamal chaired a high-level meeting of the Drug Regulatory Authority of Pakistan (DRAP), joined by the federal health secretary, additional secretary, and DRAP’s Chief Information Officer, to review preparations for this major digital transition.
During the meeting, officials evaluated the readiness for rolling out a new online system for the registration and licensing of medical devices. Minister Kamal emphasized that these reforms are part of sweeping changes underway in the health sector, underscoring that no compromise will be made on the quality of medicines and public health standards.
Highlighting the economic potential of Pakistan’s pharmaceutical and medical device industries, Kamal described the digitization of the regulatory system as a significant step towards modernization. He underscored that DRAP is being strengthened to function as an effective, transparent, and public-friendly institution.
The Health Minister also stated that efforts are being made to ensure that the public has timely access to safe and high-quality medicines. In addition, a comprehensive strategy has been developed to boost exports from the pharmaceutical and medical device sectors, further contributing to the national economy.
