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ec europa eu eurostat statistics-explained index php Medicine_use_statistics--- statista com topics 3823 drug-situation-in-europeProduct-information requirements Human Product information The European Medicines Agency (EMA) provides guidance and templates to provide marketing authorisation applicants with practical advice on how to draw up the product information for human medicines, which includes the summary of product characteristics, labelling and package leaflet If you do not, you can phone EMA on: Tel +31 (0)88 781 6000 (EMA switchboard) Tel +31 (0)88 781 7676 (for use only as stated in the instructions) Urgent phone number for use outside of EMA business hours: Tel +31 (0)65 008 9457; For full reporting instructions, see Reporting a falsified product to EMA For more information, see:The European Medicines Agency's Committee for Medicinal Products for Human Use prepares scientific guidelines in consultation with regulatory authorities in the European Union (EU) Member States, to help applicants prepare marketing authorisation applications for human medicines Guidelines reflect a harmonised approach of the EU Member States In 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 about-us about-website search-tipsThe search box accessible via 'Medicines' in the main menu and the simple medicine search on the homepage work differently They look for authorised medicines only, based on the active substance or medicine name you type in They bring up suggestions as you start typing your search word You can also initiate a search without typing in a search --- ema europa eu en about-us contacts-european-medicines-agencyeuropean-union europa eu european-medicines-agency-ema_en--- ema europa eu en product-information-requirements--- ema europa eu en partners-networks national-competent-authorities-humanNumber of staff: 897; Location: Amsterdam (the Netherlands) Website: EMA; The European Medicines Agency (EMA) protects and promotes human and animal health by evaluating and monitoring medicines within the European Union (EU) and the European Economic Area (EEA) What it doesThe 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 national competent authorities are primarily responsible for the authorisation of medicines available in the EU that do not pass through the centralised procedure They also supply thousands of European experts who serve as members of the Agency's scientific committees, working parties or in assessment teams supporting their members --- ema europa eu en human-regulatory-overview scientific-guidelines--- tevapharm com contact-usFind more information about Teva in your location   At Teva, we strive to deliver quality medicines to patients around the world with integrity and ethical business practices What we do is important, but how we do it is just as important Learn more: Teva Pharmaceuticals is pleased to answer your questions about our company and our Find the most up-to-date statistics about the drug situation in Europe Quarterly smartphone market share worldwide by vendor 2009-2023 Number of drug induced deaths in Europe in 2021, --- ema europa eu en medicines national-registers-authorised-medicines
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