The European Medicines Agency (EMA) and the Heads of Medicines Agencies (HMA) commend to national authorities, who are responsible for the authorisation of many of the medicines available in Europe that are not authorised by the European Commission on the recommendation of the (EMA). The Agency is only responsible for medicines that are managed through the central authorisation procedure.
Country | Name | Webpage |
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Austria |
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Belgium |
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Bulgaria |
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Croatia |
Agency for medicinal products and medical devices of Croatia |
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Cyprus |
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Czech Republic |
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Denmark |
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Estonia |
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Finland |
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France |
National Agency for the Safety of Medicine and Health Products |
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Germany |
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Germany |
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Greece |
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Hungary |
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Iceland |
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Ireland |
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Italy |
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Latvia |
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Liechtenstein |
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Lithuania |
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Luxembourg |
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Malta |
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Netherlands |
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Norway |
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Poland |
Office for Registration of Medicinal Products, Medical Devices and Biocidal Products |
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Poland |
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Portugal |
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Romania |
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Slovakia |
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Slovenia |
Agency for Medicinal Products and Medical Devices of the Republic of Slovenia |
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Spain |
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Sweden |
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United Kingdom |