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COVID-19: EMA recommends conditional marketing authorisation for Paxlovid

28 januar 2022

NewsHumanCOVID-19Medicines

New EU rules for safe and high-quality medicines for animals become effective

28 januar 2022

NewsVeterinaryRegulatory and procedural guidanceMedicines

Regulatory harmonisation of clinical trials in the EU: Clinical Trials Regulation to enter into application and new Clinical Trials Information System to be launched

25 januar 2022

NewsHumanClinical trials

Increase in manufacturing capacity for Vaxzevria (previously COVID-19 Vaccine AstraZeneca)

24 januar 2022

NewsHumanCOVID-19Vaccines

Meeting highlights from the Committee for Medicinal Products for Veterinary Use (CVMP) 18-19 January 2022

21 januar 2022

NewsVeterinaryMaximum residue limitMedicines

International regulators’ recommendations on COVID-19 vaccines and the Omicron variant

21 januar 2022

NewsHumanCOVID-19

COVID-19: latest safety data provide reassurance about use of mRNA vaccines during pregnancy

18 januar 2022

NewsHumanCOVID-19Vaccines

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 10 - 13 January 2022

14 januar 2022

NewsHumanCOVID-19PharmacovigilanceReferralsVaccines

EMA welcomes EU Commissioner for Health and Food Safety

13 januar 2022

NewsCorporateCOVID-19

Accelerating Clinical Trials in the EU (ACT EU): for better clinical trials that address patients’ needs

13 januar 2022

NewsHumanClinical trials