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European Medicines Agency (EMA) EMA business hours over holiday period The European Medicines Agency's (EMA) office is closed from 18:00 on 22 December to 08:30 on 5 January
Medicines | European Medicines Agency (EMA) EMA publishes information on the volume and outcome of marketing authorisation and post-authorisation applications for the human and veterinary medicines that it evaluates
Human regulatory: overview - European Medicines Agency (EMA) Information on the regulation of medicines for human use in the European Union (EU), with a focus on the centralised procedure The European Medicines Agency (EMA) plays a key role in this procedure
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
Marketing authorisation | European Medicines Agency (EMA) The European Medicines Agency (EMA) is responsible for the scientific evaluation of centralised marketing authorisation applications (MAA) Once granted by the European Commission, the centralised marketing authorisation is valid in all European Union (EU) Member States, Iceland, Norway and Liechtenstein
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
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