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Medicinal products - Latest updates (313)
RSSGlobal Gateway: European Commission and Belgian Presidency increase their support to the African Medicines Agency
Global Gateway: European Commission and Belgian Presidency increase their support to the African Medicines Agency
Commission proposes new measures for the better lifecycle management of medicine authorisations
Commission proposes new measures for the better lifecycle management of medicine authorisations
Factsheet - Steering innovation to address unmet medical needs
Factsheet - Steering innovation to address unmet medical needs
Factsheet - Addressing shortages of medicines and ensuring security of supply
Factsheet - Addressing shortages of medicines and ensuring security of supply
Factsheet - Access to medicines in all Member States
Factsheet - Access to medicines in all Member States
Factsheet - Incentives to steer innovation and achieve public health objectives
Factsheet - Incentives to steer innovation and achieve public health objectives
Summary record - 101st meeting of the Pharmaceutical Committee (23 November 2023)
Summary record - 101st meeting of the Pharmaceutical Committee (23 November 2023)
Medicines for children 2022 annual report
Medicines for children 2022 annual report
Deadline for submission extended - Open calls for expressions of interest: EMA COMP and EMA PRAC Committees
Deadline for submission extended - Open calls for expressions of interest: EMA COMP and EMA PRAC Committees
Registration and agenda - Biosimilar medicines - Multistakeholder Event (13 December 2023)
Registration and agenda - Biosimilar medicines - Multistakeholder Event (13 December 2023)
Agenda - 101st meeting of the Pharmaceutical Committee (23 November 2023)
Agenda - 101st meeting of the Pharmaceutical Committee (23 November 2023)
First electronic product information (ePIs) published for selected human medicines
First electronic product information (ePIs) published for selected human medicines
Updated document - ICH Q9 Quality Risk Management
Updated document - ICH Q9 Quality Risk Management
Updated document - Questions & Answers : Clinical Trials Regulation (EU) No 536/2014
Updated document - Questions & Answers : Clinical Trials Regulation (EU) No 536/2014
Guidance for the transition of clinical trials from the Clinical Trials Directive to the Clinical Trials Regulation
Guidance for the transition of clinical trials from the Clinical Trials Directive to the Clinical Trials Regulation
Phasing out of extraordinary COVID-19 regulatory flexibilities
Phasing out of extraordinary COVID-19 regulatory flexibilities
Agenda - Stakeholder workshop on the “Transparency Directive” (Directive 89/105/EEC) (29 June 2023)
Agenda - Stakeholder workshop on the “Transparency Directive” (Directive 89/105/EEC) (29 June 2023)
EU-US agreement on GMP inspections brings high quality medicines faster to animals
EU-US agreement on GMP inspections brings high quality medicines faster to animals
European Health Union: Commission proposes pharmaceuticals reform for more accessible, affordable and innovative medicines
European Health Union: Commission proposes pharmaceuticals reform for
more accessible, affordable and innovative medicines
Questions and Answers on the pharmaceutical legislation
Questions and Answers on the pharmaceutical legislation