104 results
-
List item
EudraGMDP database
Last updated: 01/12/2021 -
List item
Pharmacovigilance Inspectors Working Group
Last updated: 26/11/2021 -
List item
Good distribution practice
Last updated: 30/09/2021 -
List item
Compliance: Overview
Last updated: 09/04/2021 -
List item
European Directorate for the Quality of Medicines and HealthCare (EDQM) of the Council of Europe
Last updated: 09/04/2019 -
List item
Sampling and testing
Last updated: 28/03/2019 -
List item
Falsified medicines: overview
Last updated: 08/02/2019 -
List item
Press release: EU and Japan reinforce their collaboration on inspections of medicine manufacturers
Last updated: 18/07/2018 -
List item
News: Two more EU Member States benefit from EU-US mutual recognition agreement for inspections
Last updated: 01/06/2018 -
List item
Reporting a quality defect to EMA
Last updated: 03/05/2018 -
List item
Public consultation concerning the European Union template for good manufacturing practice (GMP) non-compliance statement
Last updated: 03/04/2018 -
List item
News: Four more EU Member States benefit from EU-US mutual recognition agreement for inspections
Last updated: 01/03/2018 -
List item
News: New guidelines on good manufacturing practices for advanced therapies
Last updated: 24/11/2017 -
List item
Press release: EU-US mutual recognition of inspections of medicines manufacturers enters operational phase
Last updated: 31/10/2017 -
List item
Joint Drug Information Association (DIA) / European Forum for Good Clinical Practice (EFGCP) /European Medicines Agency (EMA) conference on how to optimise children's access to innovative medicines
European Medicines Agency, London, UK, from 16/10/2017 to 17/10/2017, Last updated: 06/10/2017 -
List item
The Pharmaceutical Inspection Co-operation Scheme
Last updated: 28/09/2017 -
List item
2017 Forum on bioequivalence inspections
Continental Hotel, Budapest, Hungary, 05/10/2017, Last updated: 25/09/2017 -
List item
News: Strengthening EU-US cooperation in medicine inspections
Last updated: 23/08/2017 -
List item
Compliance: post-authorisation (veterinary medicines)
Last updated: 10/05/2017 -
List item
Compliance: marketing authorisation
Last updated: 31/03/2017 -
List item
Compliance: research and development
Last updated: 31/03/2017 -
List item
Press release: European and US regulators agree on mutual recognition of inspections of medicines manufacturers
Last updated: 02/03/2017 -
List item
News: Active pharmaceutical ingredients: Japan joins international collaboration on GMP inspections
Last updated: 25/11/2016 -
List item
2016 European Union Good Clinical Practice Inspectors Working Group workshop
European Medicines Agency, London, UK, from 17/10/2016 to 19/10/2016, Last updated: 17/10/2016 -
List item
Good Clinical Practice Inspectors Working Group
Last updated: 01/08/2016