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The European Drug Report 2024 was designed as a digital-first product, structured by modules, and optimised for online reading Within each chapter, you may download a PDF version of the page We are also making available here a PDF version of the full report (all modules and annex tables combined) ednd2 emcdda europa eu ednd loginThe agency’s general tasks in relation to drugs, drug use, drug use disorders and addictions, prevention, treatment, care, risk and harm reduction, rehabilitation, social reintegration, recovery, drug markets and supply, including illicit production and trafficking, and other relevant drug-related issues and their consequences are to: provide --- edqm eu en european-pharmacopoeia-ph -eur -11th-edition--- euda europa eu index_en--- ema europa eu en medicines--- ema europa eu en homepageOn 2 July 2024, the EMCDDA will become the new European Union Drugs Agency (EUDA) According to the report: “One of the challenges facing drug surveillance in 2024 is to gain a deeper understanding of which drugs are actually being consumed and in what combinations ” The priorities of the new Agency will include enhanced monitoring of Explore the most recent data on the drug situation in Europe provided by the EU Member States These datasets underpin the analysis presented in the agency's work Most data may be viewed interactively on screen and downloaded in Excel format European Database on New Drugs Login to EDND Username PasswordOn this page The European Drug Report 2023: Trends and Developments presents the EMCDDA’s latest analysis of the drug situation in Europe Focusing on illicit drug use, related harms and drug supply, the report contains a comprehensive set of national data across these themes and key harm reduction interventions data europa eu data datasets european-drug-report-2023-all-source-datahome-affairs ec europa eu european-drug-report-2024-latest-data-drug-situ The European Pharmacopoeia (Ph Eur ) is the primary source of official quality standards for medicines and their ingredients in Europe Ph Ph Eur standards provide a scientific basis for the quality control of a product throughout its life cycle, supporting the pharmaceutical industry and healthcare systems eur-lex europa eu EN legal-content european-union-drugs-agency-euda html--- euda europa eu publications european-drug-report 2023_en--- euda europa eu publications european-drug-report 2024_enEMA's role The 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 Login to EDND Username Password Trouble signing in? Change your password EDND support Sep 30, 2024 · Drug checking data from the Trans European Drugs Information (TEDI) network Wastewater analysis and drugs — explore the latest data EU Drug Market: Heroin and other opioids — In-depth analysis Cannabis laws in Europe : questions and answers for policymaking The European Drug Report 2024: Trends and Developments presents the EMCDDA’s latest analysis of the drug situation in Europe Focusing on illicit drug use, related harms and drug supply, the report provides a comprehensive set of national data across these themes, as well as on specialist drug treatment and key harm reduction interventions The EudraGMDP database is the Community database on manufacturing, import and wholesale-distribution authorisations, and good manufacturing-practice (GMP) and good-distribution-practice (GDP) certificates Featured news and updated for European Academics and researchers in the field of medicine development The European Medicines Agency is a decentralised agency of the European Union responsible for the evaluation, supervision and safety monitoring of medicines Our Medicine finder above helps you find information on medicines authorised for human or veterinary use You can find these by including the medicine's name or its active substance It shows you information on centrally authorised medicines - medicines that EMA evaluated You can also find information on herbal medicines Your European Union Drugs Agency (EUDA) Taking our first steps as a new EU agency! Our new mission focuses on contributing to EU preparedness on drugs through four main actions: anticipate, alert, respond and learn We are looking forward to working for you and with you Read more This is a questions and answers (Q&A) session on the Product Management Service (PMS) Product User Interface (PUI) and Application Programming Interface (API) Online European Medicines Agency, Amsterdam, the Netherlands Start date: 22 October 2024, 10:00 (CEST) End date: 22 October 2024, 10:30 (CEST) SEE ALL EVENTS European Drug Report 2023 — all source data The European Drug Report 2023: Trends and Developments presents the EMCDDA’s latest analysis of the drug situation in Europe Focusing on illicit drug use, related harms and drug supply, the report contains a comprehensive set of national data across these themes and key harm reduction interventions
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