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  2. EudraLex - Wikipedia

    en.wikipedia.org/wiki/EudraLex

    EudraLex is the collection of rules and regulations governing medicinal products in the European Union. Volumes. EudraLex consists of 10 volumes:

  3. EudraPharm - Wikipedia

    en.wikipedia.org/wiki/EudraPharm

    EudraPharm (European Union Drug Regulating Authorities Pharmaceutical Database) was the database of medicinal products authorised in the European Union, and included the information contained in the Summary of Product Characteristics, the patient or user package leaflet and the information shown on the labelling.

  4. EudraVigilance - Wikipedia

    en.wikipedia.org/wiki/EudraVigilance

    EudraVigilance (European Union Drug Regulating Authorities Pharmacovigilance) is the European data processing network and management system for reporting and evaluation of suspected adverse reactions to medicines or devices which have received marketing authorisation or are actively being studied in clinical trials in the European Economic Area (EEA).

  5. European Medicines Agency - Wikipedia

    en.wikipedia.org/wiki/European_Medicines_Agency

    Telematics projects: The Agency is responsible for implementing a central set of pan-European systems and databases such as EudraVigilance, EudraCT and EudraPharm. Centralised marketing authorisations

  6. Regulation of therapeutic goods - Wikipedia

    en.wikipedia.org/wiki/Regulation_of_therapeutic...

    Within the EU, EudraLex maintains the collection of rules and regulations governing medicinal products in the European Union, and the European Medicines Agency acts to regulate many of these rules and regulations. Amongst these rules and regulations are:

  7. List of European Union directives - Wikipedia

    en.wikipedia.org/wiki/List_of_European_Union...

    This list of European Union Directives is ordered by theme to follow EU law.For a date based list, see the Category:European Union directives by number.. From 1 January 1992 to 31 December 2014, numbers assigned by the General Secretariat of the Council followed adoption, for instance: Directive 2010/75/EU. [1]

  8. European Pharmacopoeia - Wikipedia

    en.wikipedia.org/wiki/European_Pharmacopoeia

    Cover of the European Pharmacopoeia, 11th Edition. The European Pharmacopoeia [1] (Pharmacopoeia Europaea, Ph. Eur.) is a major regional pharmacopoeia which provides common quality standards throughout the pharmaceutical industry in Europe to control the quality of medicines, and the substances used to manufacture them. [1]

  9. Regulation (European Union) - Wikipedia

    en.wikipedia.org/wiki/Regulation_(European_Union)

    EudraLex – EU laws on medicinal products; ... EUR-Lex, European Union Law database This page was last edited on 27 November 2024, at 10:02 (UTC). Text is ...