The warning comes amid reports that unregulated therapies are being offered directly to patients, potentially illegally. View ...
PathAI, a global leader in AI-powered pathology, today announced that the European Medicines Agency (EMA) Committee for Medicinal Products for Human Use (CHMP) has granted full qualification for ...
The European Union's medicines regulator on Friday reiterated its positive recommendation for Eisai and Biogen's Alzheimer's drug, Leqembi, after concluding a safety review. The European Medicines ...
The European Medicines Agency provides an interactive map with data from the information system for clinical trials. This is ...
European and US regulators are to move towards ... to encourage development of drugs for children. The FDA and EMA require all new drugs to have plans for paediatric development included ...
The EMA warns of products being sold as dendritic cell therapies with little evidence, but high health risks, in the European ...
In looking across the past four years of regulatory decisions, we noticed that some of the analyses involving the European Medicines Agency (EMA)'s cycle time used an inappropriate endpoint ...
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At its March meeting, the European Medicines Agency’s management board adopted the EMA’s annual report for 2024. This ...