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Given the wide-ranging scope of the centralised procedure, most genuinely innovative medicines marketed in Europe are authorised by the EMA The Agency fulfils its responsibilities by: facilitating the development of medicines & access to themEMA business hours over Easter holiday period The European Medicines Agency's (EMA) office is closed from 18:30 on Wednesday 27 March 2024 to 07:30 on Tuesday 2 April 2024 Outside of working hours and on public holidays, it is possible to call the product emergency hotline on +31 (0)88 781 7600 26 March 2024 Our Customer Service is available Monday to Friday 9am - 4pm If you need urgent assistance, do not use this service Call 111, or in an emergency call 999 Visit our help section Live Chat Email 01695 213 118 Avoid the appointment wait times and the pharmacy queues with EU Meds Choose from our extensive range of treatments for a prompt ec europa eu eurostat statistics-explained index php Medicine_use_statisticsThere is no specific form or format for a prescription you will use in another EU country In most cases, the prescription you would use in the country where the prescription was issued should already contain enough information for you to use it in another EU country It has to contain at least the following information: Patient details This priority area has been further enhanced as compared to the 2013-2020 strategy, to respond to the challenging developments in European drug markets These are characterised by a high availability of various types of drugs, ever larger seizures, increasing use of violence and huge profits, as well as the use of social media platforms, apps and the internet and darknet for illicit drug The national medicine registers in the different Member States of the European Union (EU) and European Economic Area (EEA) contain information on medicines authorised in those countries, including links for the summary of product characteristics (SmPC) and the package leaflet This complements information on medicines published on this website The Interreg Euro-MED Programme uses Jems, the monitoring tool developed by Interact It is available for all applicants and partners at: ---s: jems interreg-euro-med eu You can find more information in the Jems portal You can read the user manual and watch tutorials here: General documentation For national controllers, you can read the --- ema europa eu en homepagePrior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency (EMEA) [4] [5] 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) the work of existing national medicine regulatory european-union europa eu european-medicines-agency-ema_enen wikipedia org wiki European_Medicines_AgencyIn the Baltic and Nordic Member States, as well as in Hungary and Germany, at least 38 0 % of the population aged 15–24 years used non-prescribed medicines Non-prescribed medicine use was highest in 2019 among the EU population aged 35–44 years and 25–34 years, with shares of 35 6 % and 35 0 % respectively --- ema europa eu en medicines national-registers-authorised-medicineseuropa eu youreurope citizens health index_en htm--- ema europa eu en medicinesThe European Medicines Agency (EMA) facilitates development and access to medicines for countries within the European Union (EU) EMA evaluates applications for marketing authorisation submitted via the centralised procedure, monitors the safety of medicines across their lifecycle and provides information to healthcare professionals and patients interreg-euro-med eu en documents-toolseumeds com--- consilium europa eu council-approves-the-eu-drugs-strategy-for-2021-2025
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