52 results
-
List item
Committee for Medicinal Products for Human Use (CHMP): 21-24 March 2022
European Medicines Agency, Amsterdam, the Netherlands, from 21/03/2022 to 24/03/2022, Last updated: 12/08/2022 -
List item
Pharmacovigilance Risk Assessment Committee (PRAC): 25-29 September 2017
European Medicines Agency, London, UK, from 25/09/2017 to 29/09/2017, Last updated: 06/09/2017 -
List item
Pharmacovigilance Risk Assessment Committee (PRAC): 7-10 June 2021
European Medicines Agency, Amsterdam, the Netherlands, from 07/06/2021 to 10/06/2021, Last updated: 07/06/2021 -
List item
Committee for Medicinal Products for Human Use (CHMP): 12-15 October 2020
Virtual meeting, from 12/10/2020 to 15/10/2020, Last updated: 16/10/2020 -
List item
Pharmacovigilance Risk Assessment Committee (PRAC): 9-12 March 2015
European Medicines Agency, London, UK, from 09/03/2015 to 12/03/2015, Last updated: 13/03/2014 -
List item
Pharmacovigilance Risk Assessment Committee (PRAC): 3-6 July 2017
European Medicines Agency, London, UK, from 03/07/2017 to 06/07/2017, Last updated: 13/03/2014 -
List item
Pharmacovigilance Risk Assessment Committee (PRAC): 3-6 April 2017
European Medicines Agency, London, UK, from 03/04/2017 to 06/04/2017, Last updated: 13/03/2014 -
List item
Pharmacovigilance Risk Assessment Committee (PRAC): 6-9 October 2014
European Medicines Agency, London, UK, from 06/10/2014 to 09/10/2014, Last updated: 13/08/2013 -
List item
Download medicine data
Last updated: 02/12/2021 -
List item
Ninth stakeholder forum on the pharmacovigilance legislation
European Medicines Agency, London, UK, 15/09/2015, Last updated: 13/01/2016 -
List item
Pharmacovigilance Risk Assessment Committee (PRAC): 5-8 October 2015
European Medicines Agency, London, UK, from 05/10/2015 to 08/10/2015, Last updated: 13/03/2014 -
List item
Pharmacovigilance Risk Assessment Committee (PRAC): 10-13 May 2016
European Medicines Agency, London, UK, from 10/05/2016 to 13/05/2016, Last updated: 13/03/2014 -
List item
News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 7-10 March 2022
PRAC, Last updated: 11/03/2022 -
List item
Pharmacovigilance Risk Assessment Committee (PRAC): 9-12 July 2018
European Medicines Agency, London, UK, from 09/07/2018 to 12/07/2018, Last updated: 13/03/2014 -
List item
PRAC: meeting archive 2015-2017
Last updated: 13/05/2016 -
List item
Press release: European Agency for the Evaluation of Medicinal Products: Committee for Proprietary Medicinal Products -Meeting of 17 and 18 December 2002
Last updated: 19/12/2002desloratadine (Azomyr, Opulis, Allex, Aerius and Neoclarityn) from SP … -
List item
Press release: European Agency for the Evaluation of Medicinal Products: Committee for Proprietary Medicinal Products - Meeting of 17 and 18 December 2002
Last updated: 19/12/2002desloratadine (Azomyr, Opulis, Allex, Aerius and Neoclarityn) from SP … -
List item
Annual reports and work programmes (updated)
Last updated: 15/05/2023 -
List item
Committee for Medicinal Products for Human Use (CHMP): 7-10 December 2020
Virtual meeting, from 07/12/2020 to 10/12/2020, Last updated: 04/11/2019 -
List item
Press release: 67th meeting of the Committee for Proprietary Medicinal Products (CPMP)
Last updated: 31/01/2001 -
List item
News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 7-10 June 2021
PRAC, Last updated: 11/06/2021 -
List item
Committee for Medicinal Products for Human Use (CHMP): 20-23 March 2017
European Medicines Agency, London, UK, from 20/03/2017 to 23/03/2017, Last updated: 20/03/2017 -
List item
Guidance documents
Last updated: 19/07/2022 -
List item
Public data from Article 57 database
Last updated: 17/10/2022 -
List item
CHMP: meeting archive 2001-2009
Last updated: 18/11/2013