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Bookmark or Share- The European Medicines Agency's EU conditional marketing ... - The LancetExtraordinary efforts by scientists, regulators, and developers enabled the European Medicines Agency (EMA) to recommend the first EU conditional marketing authorisation (CMA) for the BioNTech COVID-19 mRNA vaccine (nucleoside-modified) BNT162b2 (Comirnaty)1 some 9 months after the COVID-19 pandemic was declared.
- Health Union: a stronger role for the European Medicines AgencyThe European Medicines Agency (EMA) will be better equipped to monitor and mitigate shortages of medicinal products and medical devices considered to be critical in order to address public health emergencies.
- Who we are - European Medicines Agency (EMA)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.
- European Medicines Agency – EMA | European UnionThe 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). The Agency's main responsibilities are authorising and monitoring medicines in the EU.
- Medicines | European Medicines Agency (EMA)Check the national registers of authorised medicines for finding medicines authorised via national procedures. The European Medicines Agency (EMA) facilitates development and access to medicines for countries within the European Union (EU).
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