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The European Medicines Agency (EMA) protects and promotes human and animal health by evaluating and monitoring medicines within the European Union (EU) and the European Economic Area (EEA). What it does. The Agency's main responsibilities are authorising and monitoring medicines in the EU.
The European Medicines Agency (EMA) operates as a decentralised scientific agency (as opposed to a regulatory authority) of the European Union (EU) and its main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary use. [8] .
Nov 30, 2021 · The EMA recently recommended that a booster dose of the two mRNA-based COVID-19 vaccines ( Comirnaty-BioNTech/Pfizer and Spikevax - Moderna) may be given to people with severely weakened immune systems as well as the general population over 18 years old, said Emer Cooke.
If the bill is signed by the Governor, this program will go into effect July 1, 2024 and applications for the 2024-25 school year will be available in the fall. Click here to learn more and join our pre-registration list to be informed when applications become available. Log in to EMA.
About us. The European Medicines Agency (EMA) is a decentralised body of the European Union with headquarters in Amsterdam. Its main responsibility is the protection and promotion of public...
The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU) responsible for the scientific evaluation, supervision and safety monitoring of medicines in the EU. EMA is governed by an independent Management Board. Its day-to-day operations are carried out by the EMA staff, overseen by EMA's Executive Director.
Video content published by the European Medicines Agency.
