The Info List - European Medicines Agency

--- Advertisement ---

Council of the EU Presidency


General Foreign Justice and Home Economic


Legislative procedure Voting Secretariat


Uwe Corsepius

Directorates-general COREPER


Court of Justice

Members Rulings

General Court

Central Bank

President Draghi

ESCB Euro EMU Eurozone

Court of Auditors

Budget OLAF

Other bodies

Agencies Investment Bank CoR EESC Ombudsman National parliaments

Policies and issues

Foreign relations

High Representative

Federica Mogherini

Ext. Action Service Foreign Policy Defence Policy Customs Union Enlargement

Budget Four Freedoms

Economic Area Area of FS&J Schengen Area


Agricultural Energy Fisheries Regional


Identity Pro-Europeanism Euroscepticism


Supranationalism Federalism United States of Europe Multi-speed Opt-outs Enhanced co-op Withdrawal


1979, 1984, 1989 1994, 1999, 2004, 2009 2014 (last election) Political parties Constituencies



Treaty on European Union Acquis

Primacy Subsidiarity


Rome Single European Act Maastricht Amsterdam Nice Lisbon

Article 50

Fundamental Rights Membership Treaties of Accession

1972, 1979, 1985, 1994, 2003, 2005, 2011

European Council

President Tusk (EPP)

Parties List of meetings

Other countries Atlas

v t e

The European Medicines Agency
European Medicines Agency
(EMA) is a European Union
European Union
agency for the evaluation of medicinal products. Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency (EMEA).[1][2] The EMA was set up in 1995 with funding from the European Union
European Union
and the pharmaceutical industry, as well as indirect subsidy from member states, in an attempt to harmonise (but not replace) the work of existing national medicine regulatory bodies. The hope was that this plan would not only reduce the €350 million annual cost drug companies incurred by having to win separate approvals from each member state but also that it would eliminate the protectionist tendencies of sovereign states unwilling to approve new drugs that might compete with those already produced by domestic drug companies. The EU is currently the source of about one-third of the new drugs brought onto the world market each year.[citation needed] Based in London, the EMA was founded after more than seven years of negotiations among EU governments and replaced the Committee for Proprietary Medicinal Products and the Committee for Veterinary Medicinal Products, though both of these were reborn as the core scientific advisory committees. After the United Kingdom
United Kingdom
withdrawal from the European Union
European Union
referendum the agency will relocate to Amsterdam. the transfer to the Netherlands
should take place in March 2019, but some complications (the city of Amsterdam
will not be ready for this period), have led the Italian government and the Municipality of Milan
to appeal. [3][4]


1 Operations 2 Centralised marketing authorisations 3 Committees

3.1 Committee for Medicinal Products for Human Use 3.2 Committee for Medicinal Products for Veterinary Use 3.3 Committee on Orphan Medicinal Products 3.4 Committee on Herbal Medicinal Products 3.5 Paediatric Committee 3.6 Committee for Advanced Therapies 3.7 Pharmacovigilance Risk Assessment Committee

4 Other activities 5 Brexit 6 Comparison with other regulatory agencies 7 See also 8 References 9 Further reading 10 External links

Operations[edit] The EMA operates as a decentralised scientific agency (as opposed to a regulatory authority) of the European Union
European Union
and its main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary use. More specifically, it coordinates the evaluation and monitoring of centrally authorised products and national referrals, developing technical guidance and providing scientific advice to sponsors. Its scope of operations is medicinal products for human and veterinary use including biologics and advanced therapies, and herbal medicinal products. The agency is composed of the Secretariat (ca. 600 staff), a management board, seven scientific committees (human, veterinary and herbal medicinal products, orphan drugs, paediatrics, advanced therapies and pharmacovigilance risk assessment) and a number of scientific working parties. The Secretariat is organised into five units: Directorate, Human Medicines Development and Evaluation, Patient Health Protection, Veterinary Medicines and Product Data Management, Information and Communications Technology and Administration. The Management Board provides administrative oversight to the Agency: including approval of budgets and plans, and selection of Executive Director. The Board includes one representative of each of the 28 Member States, two representatives of the European Commission, two representatives of the European Parliament, two representatives of patients' organisations, one representative of doctors' organisations and one representative of veterinarians' organisations. The Agency decentralises its scientific assessment of medicines by working through a network of about 4500 experts throughout the EU. The EMA draws on resources of over 40 National Competent Authorities (NCAs) of EU Member states. Centralised marketing authorisations[edit] The centralised procedure allows companies to submit a single application to the agency to obtain from the European Commission
European Commission
a centralised (or 'Community') marketing authorisation (MA) valid in all EU and European Economic Area
European Economic Area
(EEA)-European Free Trade Association (EFTA) states (Iceland, Liechtenstein
and Norway). The centralised procedure is compulsory for all medicines derived from biotechnology and other high-tech processes, as well as for human medicines for the treatment of HIV/AIDS, cancer, diabetes, neurodegenerative diseases, auto-immune and other immune dysfunctions, and viral diseases, and for veterinary medicines for use for growth or yield enhancers. The centralised procedure is also open to products that bring a significant therapeutic, scientific or technical innovation, or is in any other respect in the interest of patient or animal health. As a result, the majority of genuinely novel medicines are authorised through the EMA. For products eligible for or requiring centralised approval, a company submits an application for a marketing authorisation to the EMA. Committees[edit] Committee for Medicinal Products for Human Use[edit] A single evaluation is carried out through the Committee for Medicinal Products for Human Use (CHMP). If the Committee concludes that the quality, safety and efficacy of the medicinal product is sufficiently proven, it adopts a positive opinion. This is sent to the European Commission to be transformed into a marketing authorisation valid for the whole of the EU. A special type of approval is the paediatric-use marketing authorisation (PUMA), which can be granted for medical products intended exclusively for paediatric use.[5] The CHMP is obliged by the regulation to reach decisions within 210 days, though the clock is stopped if it is necessary to ask the applicant for clarification or further supporting data. Committee for Medicinal Products for Veterinary Use[edit] The Committee for Medicinal Products for Veterinary Use (CVMP) operates in analogy to the CHMP as described above. Committee on Orphan Medicinal Products[edit] The Committee on Orphan Medicinal Products
Committee on Orphan Medicinal Products
(COMP) administers the granting of orphan drug status since 2000. Companies intending to develop medicinal products for the diagnosis, prevention or treatment of life-threatening or very serious conditions that affect not more than five in 10,000 persons in the European Union
European Union
can apply for 'orphan medicinal product designation'. The COMP evaluates the application and makes a recommendation for the designation which is then granted by the European Commission.[citation needed] Committee on Herbal Medicinal Products[edit] The Committee on Herbal Medicinal Products (HMPC) assists the harmonisation of procedures and provisions concerning herbal medicinal products laid down in EU Member States, and further integrating herbal medicinal products in the European regulatory framework since 2004. Paediatric Committee[edit] The Paediatric Committee (PDCO) deals with the implementation of the paediatric legislation in Europe Regulation(EC) No 1901/2006 since 2007. Under this legislation, all applications for marketing authorisation of new medicinal products, or variations to existing authorisations, have to either include data from paediatric studies previously agreed with the PDCO, or obtain a PDCO waiver or a deferral of these studies. Committee for Advanced Therapies[edit] The Committee for Advanced Therapies (CAT) was established in accordance with Regulation (EC) No 1394/2007 on advanced-therapy medicinal products (ATMPs) such as gene therapy, somatic cell therapy and tissue engineered products. It assesses the quality, safety and efficacy of ATMPs, and follows scientific developments in the field. Pharmacovigilance Risk Assessment Committee[edit] A seventh committee, the Pharmacovigilance Risk Assessment Committee (PRAC) has come into function in 2012 with the implementation of the new EU pharmacovigilance legislation (Directive 2010/84/EU). Other activities[edit] The Agency carries out a number of activities, including: Pharmacovigilance The Agency constantly monitors the safety of medicines through a pharmacovigilance network and EudraVigilance, so that it can take appropriate actions if adverse drug reaction reports suggest that the benefit-risk balance of a medicine has changed since it was authorised. Referrals The Agency coordinates arbitration procedures relating to medicinal products that are approved or under consideration by Member States in non-centralized authorisation procedures. Scientific Advice Companies wishing to receive scientific advice from the CHMP or CVMP on the appropriate tests and studies to carry out in the development of a medicinal products can request it prior to or during the development program. Telematics projects The Agency is responsible for implementing a central set of pan-European systems and databases such as EudraVigilance, EudraCT and EudraPharm. Brexit[edit] Following the 2016 decision of the United Kingdom
United Kingdom
to negotiate to leave the European Union
European Union
("Brexit"), the EMA chose to search for another base of operations. According to EU Law the European Commission had to decide on the fate of the EMA's location. The EU ministers met to vote on their preferred successor.[6] The EU's Health Commissioner Vytenis Andriukaitis
Vytenis Andriukaitis
said that the preferred choice would be a location where an "easy set up and guarantee of smooth operations" would be available. Member states who had expressed their bid for the new EMA location were Austria,[7] Belgium,[8] Bulgaria,[9] Croatia,[7] Cyprus,[7] Czech Republic,[7] Denmark,[7] Finland,[10] France,[7] Germany,[7] Greece,[7] Hungary,[7] Ireland,[7] Italy,[7] Malta,[7] the Netherlands,[11] Poland,[9] Portugal,[12] Romania,[13][14] Slovakia,[7] Slovenia,[7] Spain,[7] and Sweden.[15][16][17] It had also been speculated that the Strasbourg-based seat for the European Parliament
European Parliament
could be moved to Brussels, in exchange for the city to host the EMA.[18] Others speculated on the merits of Amsterdam, well before the final decision was made.[19][20] The decision on the relocation was made on 20 November 2017 during the EU general affairs council meeting.,[21] after 3 voting rounds and finally drawing of lots. After the first round of voting, Milan
(25 votes), Amsterdam
(20 votes) and Copenhagen
(20 votes) were the only contenders left.[22] After the second voting round, two cities were left: Milan
(12 votes) and Amsterdam
(9 votes). These two cities tied in the subsequent vote (13 votes each), after which a drawing of lots identified Amsterdam
as the host city of EMA. It is unclear what future arrangements the United Kingdom
United Kingdom
proposes to make for its own medicinal evaluation after leaving the EU. Paul Workman, the president of the London-based Institute of Cancer Research, has suggested that pharmaceutical companies would naturally seek regulatory approval for new drugs in the biggest markets first, leaving the UK facing delays in approval if they set up independent arrangements.[23] Comparison with other regulatory agencies[edit] The EMA is roughly parallel to the drug part of the U.S. Food and Drug Administration (FDA),[24] but without centralisation.[25] The timetable for product approval via the EMA's centralised procedure of 210 days compares well with the average of 500 days taken by the FDA to evaluate a product.[26] See also[edit]

Ethics Committee EudraCT EudraGMP EudraLex EUDRANET EudraPharm EudraVigilance European and Developing Countries Clinical Trials Partnership European Clinical Research Infrastructures Network European Federation of Pharmaceutical Industries and Associations European Forum for Good Clinical Practice (EFGCP) ICH Inverse benefit law Medicines and Healthcare Products Regulatory Agency
Medicines and Healthcare Products Regulatory Agency
(MHRA, UK) Qualified person Regulation of therapeutic goods Supplementary protection certificate (SPC) European Banking Authority


^ Set up by EC Regulation No. 2309/93 as the European Agency for the Evaluation of Medicinal Products, and renamed by EC Regulation No. 726/2004 to the European Medicines Agency, it had the acronym EMEA until December 2009. The European Medicines Agency
European Medicines Agency
does not call itself EMA either – it currently has no official acronym but may reconsider if EMA becomes commonly accepted (see communication on new visual identity Archived 1 June 2010 at the Wayback Machine. and logo Archived 25 December 2009 at the Wayback Machine.). ^ http://www.pmlive.com/pharma_news/emea_becomes_ema_197492 ^ http://uk.reuters.com/article/us-britain-eu-pharmaceuticals-idUKKBN1771XM ^ "EMA to relocate to Amsterdam, the Netherlands" (PDF). European Medicines Agency. 20 November 2017.  ^ "Questions and answers on the paediatric use marketing authorisation (PUMA)" (PDF). European Medicines Agency. 13 September 2011.  ^ " European Council
European Council
- Offers to host the European Medicines Agency (EMA)". Retrieved 2017-09-14.  ^ a b c d e f g h i j k l m n o "Reuters - Twenty-one countries vie to host EU drug agency after Brexit". Retrieved 2017-08-10.  ^ http://www.ematobe.eu ^ a b " European Council
European Council
- Offers to host the European Medicines Agency (EMA)". Retrieved 2017-08-10.  ^ " Finland
is an excellent place for European Medicines Agency". Sosiaali- ja terveysministeriö. Retrieved 2017-04-18.  ^ "Homepage - The Dutch Bid for EMA". The Dutch Bid for EMA. Retrieved 2017-07-13.  ^ "Countries line up to host European Medicines Agency
European Medicines Agency
after it leaves UK". 15 February 2017. Retrieved 8 May 2017.  ^ " Romania
looks to poach EU medicines agency from UK". 23 March 2017. Retrieved 8 May 2017.  ^ "A Brexit
pill for Romania". 13 April 2017. Retrieved 8 May 2017.  ^ Patrick Wintour. "Countries line up to host European Medicines Agency after it leaves UK World news". The Guardian. Retrieved 2017-04-01.  ^ Julia Bradshaw (2016-12-08). " Sweden
launches campaign to host EU drugs agency instead of UK after Brexit". Telegraph.co.uk. Retrieved 2017-04-01.  ^ Andreja Zapcic (29 March 2017). "Kujundžić: Hrvatska je spremna preuzeti Europsku agenciju za lijekove". Tportal.hr. Retrieved 1 April 2017.  (in Croatian) ^ " Strasbourg
could trade Parliament seat for medicines agency".  ^ "PharmaTimes, 27th September 2017. EMA staff favour move to Amsterdam". Retrieved 19 October 2017.  ^ "Nature News, October 2017. European drug regulation at risk of stalling as agency prepares to leave London". Retrieved 13 October 2017.  ^ "Nature News, October 2017. European drug regulation at risk of stalling as agency prepares to leave London". Retrieved 13 October 2017.  ^ "Ema, Milano passa al secondo turno di votazioni con Amsterdam
e Copenhagen". Retrieved 20 October 2017.  ^ "Brexit: People will die because of plans to set up UK-only drug regulator, cancer specialist warns". Independent. 10 February 2017. Retrieved 11 February 2017.  ^ Gu, A; Patel, D; Nayak, R (2016). "Chapter 10: Drug shortages". In Fulda, TR; Lyles, A; Wertheimer. Pharmaceutical Public Policy. CRC Press. pp. 151–160. ISBN 9781498748513.  ^ Boslaugh, SE (2015). "European Medicines Agency". The SAGE Encyclopedia of Pharmacology and Society. SAGE Publications. ISBN 9781506346182.  ^ Sherwood, Ted (16 April 2008). "Generic Drugs: Overview of ANDA Review Process" (PDF). CDER Forum for International Drug Regulatory Authorities. Food and Drug Administration, Office of Pharmaceutical Science. Retrieved 30 January 2010. 

Further reading[edit]

McCormick, John (2004). The European Union: Politics and Policies. Boulder, Colo: Westview Press. ISBN 0-8133-4202-3. 

External links[edit]

Official website Heads of Medicines Agencies The Rules Governing Medicinal Products in the European Union (EudraLex) Health-EU Portal
official public health portal of the European Union

v t e

Agencies of the European Union


Safety and Health at Work Vocational Training Centre Living and Working Conditions Environment Training Foundation Drug Addiction Medicines Intellectual Property Plant Variety Translation Food Safety Maritime Safety Aviation Safety Information Security Disease Prevention and Control Satellite Navigation Railways Border and Coast Guard Asylum Support Office Fisheries Chemicals Gender Equality Fundamental Rights Defence Security Studies Satellite Centre Law Enforcement Training Law Enforcement Cooperation Judicial co-operation Energy Regulators Electronic Communications Regulators Banking Authority Securities and Markets Authority Insurance and Pensions Authority Innovation and Technology


Space (currently separate organisation)


Competitiveness and Innovation Education, Audiovisual and Culture Health and Consumers Innovation and Networks (Transport) Research Council


Euratom Supply Agency ITER
and Fusion Energy (Fusion for Energy)


Reconstruction (transferred to DG Enlargement)

Authority control

WorldCat Identities VIAF: 135204604 LCCN: nr96029968 ISNI: 0000 0001 2290 2003 GND: 1234938-0 SUDOC: 03495600X BNF: cb12565285h (data) NDL: 0089