The European Medicines Agency has started a review of medicines containing finasteride and dutasteride following concerns ...

Czechia proposes changes that will better define the role of patient organisations when informing patients about therapeutic procedures without violating advertising regulations.

The EMA anticipates that the ability to access scientific advice will foster innovation among medical device manufacturers.

Daewoong Pharmaceutical (Co-CEOs Seongsoo Park and Chang-Jae Lee), a leading healthcare company in Korea, announced the ...

One area that medical device manufacturers often overlook in post-market surveillance (PMS) planning for EU MDR and EU IVDR ...

Valneva’s chikungunya vaccine Ixchiq has been greenlit by the UK’s Medicines and Healthcare products Regulatory Agency (MHRA) ...

The proposed guidance aims to provide a framework for the approval of personalised mRNA-based cancer vaccines.

The European Medicines Agency (EMA) announced on Monday that it will be discontinuing its presence on X, opting instead to utilize rival platform Bluesky.

“Very simply, on the one side, the European Union and its member states ... our own decision making, our own evaluation on what is needed around the globe in our view, and we have all our ...

you are required to have a course-by-course evaluation completed by an approved transcript evaluation agency. Precise, word-for-word English translations of all non-English language documents are ...

This report presents the findings from the evaluation of the pilot project that the Food Standards Agency (FSA) has completed to test a proposed food standards delivery model in Wales. The aim of the ...