The field of Regulatory science ensures that medicines, vaccines, and health products are safe and effective for people to ...

The US, EU and UK operate under different systems, with distinct expectations for clinical evidence, timelines and commercial ...

Discover the EMA's role in promoting safe medicine access in the EU. Learn about its responsibilities in drug evaluation, ...

The new African Medicines Agency (AMA), is set up to strengthen medical and health security for the continent when it launches next week, experts say. The AMA, due to be officially launched during the ...

UK MHRA updates guidance on the Health Institution Exemption to support safe use of medical devices: United Kingdom Friday, December 19, 2025, 12:00 Hrs [IST] Patients across Engl ...

The World Health Organization (WHO) has officially designated Health Canada, the Ministry of Health, Labour and Welfare/Pharmaceuticals and Medical Devices Agency (MHLW/PMDA) of Japan, and the ...

As with any medicine, the MHRA will keep the safety and effectiveness of depemokimab under close review. The Medicines and Healthcare products ...

Open drug markets contribute significantly to the circulation of counterfeit medicines, posing a serious threat to public ...

The Medicines and Healthcare products Regulatory Agency (MHRA) highlighted the example of warfarin, a drug commonly used to ...

Updated MHRA guidance will help health institutions, such as NHS Trusts and Boards, safely design and make general medical devices for patients ...