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Rezultati (3839)

Regulatory information - eSubmission Gateway or web client mandatory for all eCTD submissions through the centralised procedure from 1 March 2014

7 Februar 2014

NewsCorporate

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 3-6 February 2014

7 Februar 2014

NewsHumanPharmacovigilance

Committee for orphan medicines – overview of 2013 and looking ahead

3 Februar 2014

NewsHumanRare diseases

Regulatory information - EMA announces next steps for the maintenance of information on authorised medicines by marketing-authorisation holders

31 Januar 2014

NewsCorporate

Who are the originators of innovative medicines in the EU?

31 Januar 2014

NewsCorporateInnovation

EMA releases guidance on the use of pharmacogenomics to improve safety monitoring of medicines

30 Januar 2014

NewsHuman

European Medicines Agency publishes minutes of CHMP, CVMP and CAT meetings for the first time

28 Januar 2014

NewsCorporateAdvanced therapiesMedicines

Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 20-23 January 2014

24 Januar 2014

NewsHuman

Review of emergency contraceptives started

24 Januar 2014

Press releaseHuman

EMA recommends 81 medicines for marketing authorisation in 2013

20 Januar 2014

NewsCorporate