February 5, 2025 - Valneva SE (Nasdaq: VALN; Euronext Paris: VLA), a specialty vaccine company, today announced that the Medicines and Healthcare products Regulatory Agency (MHRA) ...

Imfinzi recommended for approval in the EU by CHMP as first and only immunotherapy for limited-stage small cell lung cancer Recommendation based on ADRIATIC Phase III trial results which ...

If authorised, Vimkunya would be the first vaccine in the EU to protect adolescents aged 12 to 17 against Chikungunya.

Once every four weeks maintenance dosing may be easier for patients and care partners to continue treatment Alzheimer's disease progression does ...

On his first day in office, President Donald Trump signed an executive order withdrawing the U.S. from the World Health Organization ... the FDA and EMA [European Medicines Agency], they wanted ...

Thank you for completing the survey. Click the links below to download your 2014 European Radio Frequency Allocations Charts. Charts Include: 3-3000 kHz, 3-30 MHz, 30-3000 MHz, 3-30 GHz and 30-300 ...

Good morning. It’s a comparatively light day in the House of Commons so both Kemi Badenoch and Ed Davey have opted to try to get their issues talked about today via set-piece speeches.

The European Union’s AI Act has requirements that begin to apply from 2 February 2025 and will have regulatory implications for AI globally. For medicines development, the act will affect AI ...

The number of irregular border crossings into the European Union fell significantly in 2024, according to the bloc’s border control agency Frontex, something which it attributed to intensified ...

Today, we announced our submission of a marketing authorization application for DAYBUE with the European Medicines Agency and anticipate beginning Managed Access Program–related sales in Europe ...

SAN DIEGO--(BUSINESS WIRE)--Acadia Pharmaceuticals Inc. (Nasdaq: ACAD) today announced that the company has submitted a Marketing Authorization Application (MAA) to the European Medicines Agency ...