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Phasing out of extraordinary COVID-19 regulatory flexibilities

6 juli 2023

News Human COVID-19

Global regulators confirm good safety profile of COVID-19 vaccines

5 juli 2023

News Human COVID-19 Medicines

Use of real-world evidence in regulatory decision making – EMA publishes review of its studies

23 juni 2023

News Human Data on medicines

Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 19-22 June 2023

23 juni 2023

News Human Medicines

ACT EU: creating a better environment for clinical trials through collaboration

22 juni 2023

News Human Clinical trials

Report: How EU ensured safety of medicines during COVID-19

22 juni 2023

News Human Pharmacovigilance

Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 13-15 June 2023

16 juni 2023

News Veterinary Maximum residue limit Medicines

EMA Management Board: highlights of June 2023 meeting

9 juni 2023

News Corporate

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 5 - 8 June 2023

9 juni 2023

News Human Pharmacovigilance Referrals

EMA and ECDC statement on updating COVID-19 vaccines to target new SARS-CoV-2 virus variants

7 juni 2023

News Human COVID-19 Vaccines