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Pharmeuropa 36 2: the issue is now complete (public enquiry until 30 June 2024) Pharmeuropa 36 1: drafts texts are now found in Pharmeuropa archives Test for extractable volume of parenteral preparations (2 9 17 ) (until 30 June 2024) General information Harmonisation status for General Texts --- ema europa eu en homepage--- emcdda europa eu edr2020_enThe countdown to the EU Drugs Agency (EUDA) is on! On Tuesday 2 July 2024, the EMCDDA will become the European Union Drugs Agency (EUDA), with a new mandate and stronger role Check out our web page which explains what this change means and provides practical information for all of our customers, partners and stakeholders Drugs are a complex social and health phenomenon that affects millions of peoplein the EU Illicit drugs can have tremendous negative consequences, not only for the people who use the drugs but also for their families and communities The use of drugs generates enormous costs for and harm topublic health and safety, the environment and labour produ This report, available in 24 languages, presents a summary of some the main findings of the 'European Drug Report 2020: Trends and Developments', the EMCDDA’s latest analysis of the drug situation in Europe The issues selected here have been chosen for their policy relevance and general interest --- emcdda europa eu edr2021_enthe participation and involvement of civil society This approach was enshrined in the EU drugs strategy 2013-2020 and reaffirmed in the EU drugs strategy 2021-2025, approved by the Council in December 2020 The new strategy for 2021-2025 sets out the political framework and priorities for the EU's drug policy and complements national policies ednd2 emcdda europa eu ednd login--- ema europa eu en medicinesiris ema europa eu--- consilium europa eu en policies eu-drugs-policyDec 18, 2020 · 18 December 2020 18:20 Council approves the EU drugs strategy for 2021-2025 The Council today approved the EU strategy setting out the political framework and priorities for the EU's drug policy in the period 2021-2025 The strategy aims to ensure a high level of health promotion, social stability and security and contribute to awareness raising --- emcdda europa eu index_en 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 Statistical Bulletin 2021 The annual Statistical Bulletin contains the most recent available data on the drug situation in Europe provided by the Member States These datasets underpin the analysis presented in the European Drug Report All data may be viewed interactively on screen and downloaded in Excel format Access >> The External Organisation Administrator is a special role in the EMA Account Management portal This Administrator, once validated by EMA, can approve or reject requests to become an administrator for other EMA-run systems[ 1] for their organisation EudraVigilance: When requesting access as a Responsible Person or EU QPPV Additional QPPV register ema europa eu identityiq home htmlInspections Increase efficiency on reporting inspections data and create a better overview of scientific regulatory data by managing your inspections for GMP, GCP and GVP processes via IRIS Marketing status Report changes in the marketing status of a single product, or multiple products at the same time, for each presentation and EU Member European Drug Report 2021 (60 pages) The annual Trends and Developments report presents a top-level overview of the drug phenomenon in Europe , covering drug supply, use and public health problems, as well as drug policy and responses Download >> New benzodiazepines in Europe – a review (48 pages) Registration HumanData on medicinesRegulatory and procedural guidance Related content Related EU legislation To begin data submission on authorised medicines, marketing-authorisation holders need to register with EudraVigilance See full list on consilium europa eu 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 and patients 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 pharmeuropa edqm eu homeEuropean Database on New Drugs Login to EDND Username Change your password EDND support EMCDDA-EDND European Database on New Drugs Login to EDND Username
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