the EU regulates the authorisation of medicines at EU level via the European Medicines Agency or at national level via the competent authorities in EU countries. Once on the market, the safety of a ...

Hungary's Olivér Várhelyi will have to explain to Members of the European Parliament exactly how he will promote women’s ...

Several European countries have shown interest in Sputnik although the EU's medicines agency is yet to approve it It's no coincidence that Russia has christened its Covid vaccine Sputnik V.

ImmunityBio intends to submit to the European Medicines Agency (EMA) an MAA for ANKTIVA in the European Union (EU) in Q4 2024 ...

The integration of Artificial Intelligence (AI) into drones has revolutionised various industries, from agriculture and logistics to surveillance and defence. AI-powered drones offer advanced ...

Residents of the countries of the European Union are recommended to stock up on at least three days' worth of food in case of ...

The Swedish medicines regulator has significantly increased its EU involvement ... the agency mapped the pharmaceutical production and its capacities in Sweden and in the Nordic countries.

About AVT23 AVT23 is a monoclonal antibody and proposed biosimilar to Xolair ® (omalizumab). AVT23 is an investigational compound and has not received regulatory approval in any country. Biosimilarity ...

Efforts to address this dependency began in December when the European Medicines Agency (EMA ... have been set up to assess ...

Neurizon has been buoyed by the receipt of a positive opinion from the European Medicines Agency in relation to its ... Read ...

Neurizon Therapeutics Limited (Neurizon), a clinical-stage biotech company advancing treatments for neurodegenerative diseases, announced it has received notice of a positive opinion from the European ...

Dupixent approved in the EU as the first and only medicine for young children with eosinophilic esophagitisApproval based on phase 3 data showing ...