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This section of the website contains the European Medicines Agency's news and press releases, information on meetings and events, public consultations and related information.

For a scrolling feed of all of the new and updated information published on the website, see the what's new page.

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This month's events

February 2018

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  • 2018-02-12 - 2018-02-12 : EMA

    Submission of referentials management services (RMS) and organisations management services (OMS) change requests

    The European Medicines Agency’s (EMA) programme for substance, product, organisation and referential (SPOR) data services held a webinar with industry stakeholders to summarise the milestones and impacts on industry of the referentials management services (RMS) and organisations management services (OMS). The webinar focused on the submission of RMS and OMS change requests relating to referential and organisation data.

  • 2018-02-12 - 2018-02-14 : EMA

    The new EudraVigilance system and the electronic reporting of ICSRs in the ISO/ICH E2B(R3) format: hands-on training course

    This hands-on training course covers the functionalities of the new EudraVigilance web application (EVWEB). It includes practical examples for creating, sending and accessing ICSRs in the new ISO/ICH E2B(R3) format. It covers reporting principles in accordance with the guideline on good pharmacovigilance practices (GVP) Module VI 'Management and reporting of adverse reactions to medicinal products' and explanations on how to comply with the EudraVigilance business rules and the EudraVigilance access policy.