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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) Only medicines evaluated by EMA are available on this website You may not be able to obtain a complete list of available treatment options for a specific condition by searching on EMA's website
News | European Medicines Agency (EMA) EMA partners with healthcare professionals and consumers for #ItTakesATeam medicine shortages campaign Campaign highlights how different actors can help in case of a shortage
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
Authorisation of medicines - European Medicines Agency (EMA) While the majority of new, innovative medicines are evaluated by EMA and authorised by the European Commission in order to be marketed in the EU, most generic medicines and medicines available without a prescription are assessed and authorised at national level in the EU
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
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