35-755: The European Medicines Agency ( EMA ) is an agency of the European Union (EU) in charge of the evaluation and supervision of pharmaceutical products . Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency ( EMEA ). The EMA was set up in 1995, with funding from the European Union and the pharmaceutical industry , as well as indirect subsidy from member states, its stated intention to harmonise (but not replace)
70-493: A decentralised scientific agency (as opposed to a regulatory authority ) of the European Union (EU) 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, develops technical guidance and provides scientific advice to sponsors. Its scope of operations
105-753: A temporary building in Amsterdam, and by January 2020 the relocation to the permanent building in Amsterdam Zuidas district was finalised. The EMA played a significant role in the response to the COVID-19 pandemic in the European Union , seeking to expedite the development and approval of COVID-19 vaccines and treatments . It participated in the Accelerating COVID-19 Therapeutic Interventions and Vaccines (ACTIV) public–private partnership hosted by
140-454: 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. The EMA
175-757: 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. The CHMP
210-529: 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. It is also compulsory for advanced-therapy medicines such as gene-therapy, somatic cell-therapy or tissue-engineered medicines and for orphan medicines (for rare diseases). The centralised procedure
245-496: 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
280-645: 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. The review process of the European Medicines Agency regarding medical issues has been criticized for its lack of transparency. In a rebuttal of an EMS review that included her work, Louise Brinth, a Danish physician, noted that "experts" reviewing data remain unnamed and seem to be bound to secrecy. Minutes are not released and diverging opinions are not reported suggesting that all
315-477: 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
350-735: The Coalition for Epidemic Preparedness Innovations ' Joint Coordination Group. It is also a benefactor of Health Level Seven International , a member of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use and the International Pharmaceutical Regulators Programme (IPRP), and a partner of the Society for Immunotherapy of Cancer and Vaccine Confidence Project . A single evaluation
385-529: The European System of Financial Supervision ) London (2011–2019) ( [REDACTED] UK till 2019) Single Resolution Mechanism bodies (of the European banking union ) Common Security and Defence Policy agencies (under the former II Pillar) Executive agencies are created by European Commission for a fixed period. A joint undertaking is a juridical person and a subsidiary body of
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#1732765139088420-720: The Foundation for the National Institutes of Health , collaborating with international government agencies and corporations to coordinate a research strategy for prioritizing and speeding up development of COVID-19 vaccines and pharmaceutical products. While in the process of evaluating the Pfizer–BioNTech COVID-19 vaccine in December 2020, the EMA suffered a cyberattack , resulting in the leak of classified regulatory documents to journalists, academics and
455-448: The protectionist tendencies of Sovereign states unwilling to approve new drugs that might compete with those already produced by domestic drug companies. 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. The agency
490-573: The "experts" are of the same opinion. In her view the process is unscientific and undemocratic. The Committee for Medicinal Products for Veterinary Use (CVMP) operates in analogy to the CHMP as described above. The 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
525-828: The 194 Member States of the World Health Assembly in May 2012, and published on the World Health Organization 's website in February 2013. Following the 2016 decision of the United Kingdom to leave the 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. The EU's Health Commissioner Vytenis Andriukaitis said that
560-725: The 27 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. The EMA additionally engages with international agencies and non-governmental organizations on areas of mutual interest, such as its participation on
595-658: The Baltic States and Luxembourg). It had also been speculated that the Strasbourg -based seat for the European Parliament could be moved to Brussels, in exchange for the city to host the EMA. Others speculated on the merits of Amsterdam, well before the final decision was made. The decision on the relocation was made on 20 November 2017, during the EU General Affairs Council meeting, after three voting rounds and finally drawing of lots. After
630-528: The EU or Euratom, established through an agreement between the European Commission , the participating member states, and the European industry of a certain field, with the purpose of implementing a public-private partnership project. The list includes the two decentralised bodies other than agencies, established as EU juridical persons through secondary legislation of the EU/Euratom. The list includes
665-523: The EU, and in some cases, also across the EEA countries, Switzerland, Serbia, Ukraine, the United Kingdom and Turkey. Nevertheless, in relations with other non-EU third countries, they are in general not recognised as independent entities, thus being considered either parts of the juridical personality of the EU or Euratom. Some of the agencies, decentralised independent bodies and joint undertakings of
700-412: The European Union and Euratom ) are bodies of the European Union and Euratom established as juridical persons through secondary EU legislation and tasked with a specific narrow field of work. They are distinct from: In contrast to other EU bodies established through secondary legislation, each of more than fifty such entities has its own juridical personality granted by the EU law, recognised across
735-530: The European Union and Euratom are tasked with answering the need to develop scientific or technical know-how in certain fields, others bring together different interest groups to facilitate dialogue at European and international level. They are divided into the following groups: Distinct from the EU institutions, the agencies of the European Union are specialist bodies set up to advise the Institutions and Member States in areas that affect everyone living in
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#1732765139088770-505: The 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 . 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
805-473: The European regulatory framework since 2004. 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
840-484: The PDCO, or obtain a PDCO waiver or a deferral of these studies. 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. A seventh committee,
875-772: 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). The Agency carries out a number of activities, including: The centralised procedure allows companies to submit a single application to the agency to obtain from the European Commission a centralised (or "community") marketing authorisation (MA) valid in all European Union member states and in Iceland , Liechtenstein and Norway . The centralised procedure
910-571: The Union. They are located in member states across the EU, providing services, information, and know-how. The total budget of all the decentralised agencies is approximately 0.8% of the EU's annual budget. Single market agencies (under the former I Pillar) London (1995–2019) ( [REDACTED] UK until 2019) Area of freedom, security and justice agencies (under the former III Pillar) Bramshill (2005–2014) ( [REDACTED] UK till 2014) European supervisory authorities (of
945-574: The drug part of the U.S. Food and Drug Administration (FDA), but without centralisation . 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 in 2008 to evaluate a product. Agencies of the European Union The agencies of the European Union (formally: Agencies, decentralised independent bodies, corporate bodies and joint undertakings of
980-492: The first round of voting, Milan (25 votes), Amsterdam (20 votes) and Copenhagen (20 votes) were the only contenders left. After the second voting round, two cities were left: Milan (twelve votes) and Amsterdam (nine votes). These two cities tied in the subsequent vote (thirteen votes each), after which a drawing of lots identified Amsterdam as the host city of EMA. EMA staff left its London premises in March 2019 to relocate to
1015-574: 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 , Belgium , Bulgaria , Croatia , Cyprus , Czech Republic , Denmark , Finland , France , Germany , Greece , Hungary , Ireland , Italy , Malta , the Netherlands , Poland , Portugal , Romania , Slovakia , Slovenia , Spain , and Sweden (or in other words all remaining member countries except for
1050-407: The public via the dark web . The documents revealed internal concerns about low production quality in the mRNA vaccine candidate, and regulators' efforts to have Pfizer and BioNTech rectify these deficiencies. The EMA ultimately authorized the vaccine on 21 December 2020, satisfied that the product quality was "sufficiently consistent and acceptable." As of 2016, the EMA was roughly parallel to
1085-529: The remaining two bodies other than agencies, decentralised bodies or joint undertakings, established as EU juridical persons through secondary legislation of the EU/Euratom. Committee for Medicinal Products for Human Use The Committee for Medicinal Products for Human Use ( CHMP ), formerly known as the Committee for Proprietary Medicinal Products ( CPMP ), is the European Medicines Agency 's committee responsible for elaborating
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1120-423: 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 EMA
1155-523: 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. The agency was located in London prior to the United Kingdom's vote for withdrawal from the European Union , relocating to Amsterdam in March 2019. The European Medicines Agency (EMA) operates as
1190-541: Was located in London prior to the United Kingdom's vote for withdrawal from the European Union , relocating to Amsterdam in March 2019. Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency ( EMEA ). The EMA contributed to the Global Vaccine Action Plan developed by the Decade of Vaccines Collaboration, endorsed by
1225-448: Was set up in 1995, with funding from the European Union and the pharmaceutical industry , as well as indirect subsidy from member states, its stated intention 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
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