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The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU). It is responsible for the scientific evaluation, supervision and safety monitoring of medicines. EMA protects public and animal health in EU Member States, as well as the countries of the European Economic Area, by ensuring that all medicines available on ...
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] .
On March 18, the U.S Food and Drug Administration and the European Medicines Agency (EMA) jointly chaired the first global regulators meeting to discuss regulatory strategies to facilitate...
Jul 4, 2023 · The European Medicines Agency (EMA) is a decentralized agency of the European Union (EU) whose goal is to promote and protect human and animal health. The EMA is the European Union’s equivalent...
Mar 10, 2021 · As it conducted its analysis of the Pfizer-BioNTech covid-19 vaccine in December, the European Medicines Agency (EMA) was the victim of a cyberattack. 1 More than 40 megabytes of classified information from the agency’s review were published on the dark web, and several journalists—including from The BMJ —and academics worldwide were sent copies...
The European Medicines Agency (EMA) contributes to global efforts to protect people from COVID-19. EMA enables the development and approval of safe and effective treatments and vaccines and provides reliable information to patients and healthcare professionals in the European Union (EU). Human COVID-19.
