Filter by Keywords Search Clear filters Medicinal products - Latest updates (314) RSS Showing results 240 to 260 News announcement26 October 2017State of Paediatric Medicines in the EU1 min readNews announcement20 October 2017Advanced therapy medicinal products (ATMPs): DG SANTE and EMA launch new action plan1 min readNews announcement18 September 2017Patient safety: Commission adopts acts on Good Manufacturing Practices for medicines1 min readNews announcement23 August 2017Medicine safety: New commitment allows EU and US to share full medicine inspection reports1 min readNews announcement7 July 2017Report on activity of the Expert Group on Safe and Timely Access to Medicine for Patients (STAMP) 2015 - 20161 min readNews announcement5 July 2017Responses to the targeted stakeholder consultation on the experience acquired with the Paediatric Regulation1 min readNews announcement5 July 2017Independent Scientific experts: Call for expressions of interest for the EMA PRAC Committee1 min readNews announcement30 June 20172016 report on the application of the Paediatric RegulationNews announcement20 June 20177th Meeting of the STAMP Expert Group - Draft agenda1 min readNews announcement20 June 2017Version 7 of "Questions and Answers" document regarding the implementation of the rules on the safety features for medicinal products for human use is now available.1 min readNews announcement7 June 20176th Meeting of the STAMP Expert Group - Final record1 min readNews announcement31 May 2017Questions and Answers related to the United Kingdom's withdrawal from the European Union with regard to the medicinal products for human and veterinary use within the fra1 min readNews announcement2 May 2017Notice to marketing authorisation holders of centrally authorised medicinal products concerning the United Kingdom's notification pursuant to Article 50 of the Treaty on 1 min readNews announcement2 May 2017SCOPE E-learning for healthcare professionals and doctors1 min readNews announcement24 April 2017Report on pharmacovigilance related activities of Member States and the European Medicines Agency concerning medicinal products for human use (2012 – 2014) - Publication 1 min readNews announcement10 April 2017Euripid Project “Statistical data for medicinal product pricing” reaches half-time1 min readNews announcement23 March 2017Report to the European Parliament and the Council on the summary of product characteristics and the package leaflets1 min readNews announcement27 February 2017Targeted stakeholder consultation on the revised guidelines on excipients in the labelling and package leaflet of medicinal products for human use7 min readNews announcement24 January 2017Publication of report on 10 years of experience at the European Medicines Agency of conditional marketing authorisation for medicines for unmet medical needs1 min readNews announcement7 December 2016Live broadcast (8 December 2016 - 09:30 C.E.T.): Adaptive Pathways Workshop1 min read Previous1...111213Page 13141516Next
News announcement20 October 2017Advanced therapy medicinal products (ATMPs): DG SANTE and EMA launch new action plan1 min read
News announcement18 September 2017Patient safety: Commission adopts acts on Good Manufacturing Practices for medicines1 min read
News announcement23 August 2017Medicine safety: New commitment allows EU and US to share full medicine inspection reports1 min read
News announcement7 July 2017Report on activity of the Expert Group on Safe and Timely Access to Medicine for Patients (STAMP) 2015 - 20161 min read
News announcement5 July 2017Responses to the targeted stakeholder consultation on the experience acquired with the Paediatric Regulation1 min read
News announcement5 July 2017Independent Scientific experts: Call for expressions of interest for the EMA PRAC Committee1 min read
News announcement20 June 2017Version 7 of "Questions and Answers" document regarding the implementation of the rules on the safety features for medicinal products for human use is now available.1 min read
News announcement31 May 2017Questions and Answers related to the United Kingdom's withdrawal from the European Union with regard to the medicinal products for human and veterinary use within the fra1 min read
News announcement2 May 2017Notice to marketing authorisation holders of centrally authorised medicinal products concerning the United Kingdom's notification pursuant to Article 50 of the Treaty on 1 min read
News announcement24 April 2017Report on pharmacovigilance related activities of Member States and the European Medicines Agency concerning medicinal products for human use (2012 – 2014) - Publication 1 min read
News announcement10 April 2017Euripid Project “Statistical data for medicinal product pricing” reaches half-time1 min read
News announcement23 March 2017Report to the European Parliament and the Council on the summary of product characteristics and the package leaflets1 min read
News announcement27 February 2017Targeted stakeholder consultation on the revised guidelines on excipients in the labelling and package leaflet of medicinal products for human use7 min read
News announcement24 January 2017Publication of report on 10 years of experience at the European Medicines Agency of conditional marketing authorisation for medicines for unmet medical needs1 min read
News announcement7 December 2016Live broadcast (8 December 2016 - 09:30 C.E.T.): Adaptive Pathways Workshop1 min read