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The African Medicines Agency is a specialised agency of the African Union and its 55 Member States. It will work to improve governmental collaboration across Africa and help patients access medicines. The European Medicines Agency (EMA) and the European medicines regulatory network provide guidance, technical expertise and financial support to the...
Use this form to send a request for information from the European Medicines Agency (EMA) or to make a formal request for access to EMA documents that are not already published on this website.
The Guidelines Consistency Group (GCG) provides peer reviews for all concept papers, guidelines, reflection papers and related documents submitted for adoption to the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA). This is meant to ensure their regulatory and scientific consistency.
The European Medicines Agency's office is located in Amsterdam. Find guidance on how to get to the building and plan your visit to our office and information on the building's accessibility. For post and deliveries, we have two separate addresses.
The Pharmacovigilance Risk Assessment Committee (PRAC) is the European Medicines Agency's (EMA) committee responsible for assessing and monitoring the safety of human medicines. The Committee meets once a month. EMA publishes the agendas, minutes and highlights of its plenary meetings.
The Committee on Herbal Medicinal Products (HMPC) is the European Medicines Agency's (EMA) committee responsible for compiling and assessing scientific data on herbal substances, preparations and combinations, to support the harmonisation of the European market. The Committee meets once every two months. EMA publishes the agendas, minutes and...
The Paediatric Committee (PDCO) is the European Medicines Agency's (EMA) scientific committee responsible for activities on medicines for children and to support the development of such medicines in the European Union by providing scientific expertise and defining paediatric needs. The Committee meets once a month. EMA publishes the agendas...
The Management Board is the European Medicines Agency's integral governance body. It has a supervisory role with general responsibility for budgetary and planning matters, the appointment of the Executive Director and the monitoring of the Agency's performance. The Board generally meets four times a year. EMA publishes the agendas and minutes of...
The Committee for Medicinal Products for Human Use (CHMP) is the European Medicines Agency's (EMA) committee responsible for human medicines. It plays a vital role in the authorisation of medicines in the European Union. The committee meets once a month. EMA publishes agendas, minutes and highlights of its plenary meetings.
The Committee for Advanced Therapies (CAT) is the European Medicines Agency's (EMA) committee responsible for assessing the quality, safety and efficacy of advanced therapy medicinal products (ATMPs) and following scientific developments in the field. The Committee meets once a month. EMA publishes the agendas, minutes and meeting reports of its...