Pakistan Launches Digital Overhaul of Medical Device Registration

In a landmark move to modernize Pakistan’s healthcare sector, Prime Minister Shehbaz Sharif inaugurated the digitisation of medical device registration and licensing on July 22, 2025, as announced by the Ministry of Health. Spearheaded by Health Minister Mustafa Kamal, this initiative by the Drug Regulatory Authority of Pakistan (DRAP) aims to streamline access to safe and effective medical devices, from wheelchairs to advanced MRI machines.

A Digital Revolution in Healthcare

The new system enables fully online registration and licensing, allowing citizens to submit applications from the comfort of their homes. Previously, the process could take years, bogged down by bureaucratic delays. The digitisation effort slashes this timeline to just 20 days, ensuring faster access to high-quality medical devices and medicines.

“This is a transformative step for Pakistan’s healthcare system,” the Ministry of Health stated. “By leveraging technology, we are enhancing efficiency and ensuring the public has timely access to safe, reliable medical equipment.”

Economic and Public Health Impact

The initiative is poised to unlock significant economic potential within Pakistan’s pharmaceutical and medical device industries. By simplifying regulatory processes, the country aims to foster innovation, attract investment, and strengthen its position in the global healthcare market.

The Ministry highlighted that these reforms are part of a broader effort to modernize the health sector under Health Minister Mustafa Kamal’s leadership. The focus on digitisation not only improves accessibility but also ensures stringent quality control, aligning with international standards.

Looking Ahead

The digitisation of medical device registration marks a significant milestone in Pakistan’s ongoing healthcare reforms. By reducing bureaucratic hurdles and prioritizing efficiency, the government is paving the way for a more responsive and robust healthcare ecosystem. This initiative is expected to benefit both citizens and the industry, ensuring that essential medical devices are readily available and meet the highest safety standards.

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