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Výsledky (3794)

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

23 Červen 2023

News Human Data on medicines

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

23 Červen 2023

News Human Medicines

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

22 Červen 2023

News Human Clinical trials

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

22 Červen 2023

News Human Pharmacovigilance

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

16 Červen 2023

News Veterinary Maximum residue limit Medicines

EMA Management Board: highlights of June 2023 meeting

9 Červen 2023

News Corporate

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

9 Červen 2023

News Human Pharmacovigilance Referrals

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

7 Červen 2023

News Human COVID-19 Vaccines

Progress with EU-US mutual recognition agreement for inspections for veterinary medicines

31 Květen 2023

News Human Veterinary Corporate Compliance and inspections

Global regulators agree on way forward to adapt COVID-19 vaccines to emerging variants

30 Květen 2023

News Human COVID-19 Vaccines