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European Medicines Agency (EMA) Episode 1 of Inside EMA explores the fight against antimicrobial resistance New booklet on safety monitoring of medicines in the EU #ItTakesATeam – first campaign co-created with healthcare professional and patient organisations Campaign highlights how different actors can help in case of a shortage
Medicines | European Medicines Agency (EMA) The medicine you are looking for may be authorised in individual Member States via national procedures, rather than centrally via EMA Only medicines evaluated by EMA are available on this website
News and events - European Medicines Agency (EMA) Check EMA's annual reports for insights into our regulatory procedures, activities, and achievements The reports include an interactive timeline and figures and statistics for easy comprehension
What’s new - European Medicines Agency (EMA) Find all new and updated information published on our website in one place below Filters are available to narrow results down based on your interests, such as whether it relates to human or veterinary medicines or specific topics Information on medicines and related procedures includes a reference to relevant substances: INN or common name, active substance, and English common name for
Scientific guidelines | European Medicines Agency (EMA) EMA strongly encourages applicants and marketing authorisation holders to follow the guidelines featured on this page Applicants need to justify deviations from guidelines fully in their applications at the time of submission
COVID-19 medicines | European Medicines Agency (EMA) The European Medicines Agency (EMA) evaluates and recommends the authorisation of medicines marketed in the European Union (EU) This includes COVID-19 vaccines and treatments