EMA launches new submission portal today LONDON, 20-Jun-2018 — /EuropaWire/ — The European Medicines Agency (EMA) has launched a new secure online…
The European Medicines Agency (EMA) is currently looking for a new location in connection with the UK’s withdrawal from the…
Requirements for industry now available on submission of clinical data for publication LONDON, 04-Mar-2016 — /EuropaWire/ — The European Medicines Agency…
EMA veterinary committee sets objectives to limit risks arising from use of antimicrobials in animals LONDON, 20-11-2015 — /EuropaWire/ —…
LONDON, 14-7-2015 — /EuropaWire/ — The European Medicines Agency (EMA) has started a review of HPV vaccines to further clarify…
EMA publishes workshop report on requirements for the authorisation of vaccines LONDON, 14-7-2015 — /EuropaWire/ — The European Medicines Agency…
EMA invites feedback on its new draft guideline LONDON, 22-5-2015 — /EuropaWire/ — The European Medicines Agency (EMA) has released…
EMA to host workshop on therapeutic use of bacteriophages LONDON, 22-5-2015 — /EuropaWire/ — The European Medicines Agency (EMA) will…
Registration now open for a workshop of the European Network of Paediatric Research at the European Medicines Agency (Enpr-EMA) on…
Developers encouraged to request accelerated procedure for scientific advice LONDON, 30-10-2014 — /EuropaWire/ — The European Medicines Agency (EMA) has…
LONDON, 4-3-2014 — /EuropaWire/ — The European Medicines Agency reminds applicants and marketing-authorisation holders that adjusted fees will be coming into effect…
30-7-2013 — /EuropaWire/ — The European Medicines Agency (EMA) has published the ‘First annual report onEudraVigilance for the European Parliament, the Council…
Key deliverable of Falsified Medicines Directive achieved 22-4-2013 — /europawire.eu/ — The European Medicines Agency has upgraded its EudraGMP database so…