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1. www.ema.europa.euHomepage | European Medicines Agency

   www.ema.europa.eu

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   The European Medicines Agency (EMA) is the EU agency responsible for evaluating and supervising medicines for human and veterinary use. Find information on medicines, news, events, FAQs and more on its homepage.

   • Medicines

     Our Medicine finder above helps you find information on...

     National Registers

     · Medicines Under Evaluation

     · What We Publish and When

     · Download

     · Referrals

     · Abasaglar

   • About us

     About us. The European Medicines Agency (EMA) is a...

     Contacts

     · What We Do

     · History of EMA

     · How We Work

     · Frequently Asked Questions

     · Annual Reports and Work Programmes

   • Who We Are

     The European Medicines Agency (EMA) is a decentralised...

   • Scientific Guidelines

     The European Medicines Agency's Committee for Medicinal...

   • Marketing Authorisation

     The European Medicines Agency (EMA) is responsible for the...

   • Coronavirus Disease (COVID-19)

     The European Medicines Agency (EMA) contributes to global...

   • Good Manufacturing Practice

     Good manufacturing practice (GMP) describes the minimum...

   • CHMP

     The Committee for Medicinal Products for Human Use (CHMP) is...

   • What's New

     What’s new. Find all new and updated information published...

2. en.wikipedia.org › wiki › European_Medicines_AgencyEuropean Medicines Agency - Wikipedia

   en.wikipedia.org › wiki › European_Medicines_Agency

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   The European Medicines Agency (EMA) is an agency of the European Union (EU) in charge of the evaluation and supervision of pharmaceutical products. Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency (EMEA).

3. european-union.europa.eu › institutions-law-budgetEuropean Medicines Agency – EMA | European Union

   european-union.europa.eu › institutions-law-budget

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   The EMA evaluates and monitors medicines for humans and animals in the EU and the EEA. It issues marketing authorisations, provides safety information, and supports research and development of new medicines.

4. Videos

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     How does EMA ensure the safety of medicines in the EU

     Oct 23, 2023

     1.5K Views

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     Overview of the European Medicines Agency (EMA), Part 1 of 3

     Aug 31, 2023

     1.8K Views

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     Overview of the European Medicines Agency (EMA), Part 2 of 3

     Aug 31, 2023

     837 Views

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5. www.europarl.europa.eu › news › enDeal on stronger role for EU medicines regulator | News ...

   www.europarl.europa.eu › news › en

   Oct 28, 2021 · New EU platform to monitor and report medicine shortages. Parliament and Council reached a provisional agreement on Thursday to make the European Medicines Agency more effective in tackling shortages of medicines and medical devices.

6. www.europarl.europa.eu › news › enHealth Union: a stronger role for the European Medicines Agency

   www.europarl.europa.eu › news › en

   Jan 20, 2022 · Background. As part of building a European Health Union, the Commission proposed on 11 November 2020 a new health security framework fit for future health challenges, based on lessons learnt from combatting COVID-19, which includes a proposal to increase the powers of the European Medicines Agency.

7. People also ask

   What is the European Medicines Agency (EMA)?

   • The European Medicines Agency (EMA) facilitates development and access to medicines for countries within the European Union (EU). EMA evaluates applications for marketing authorisation submitted via the centralised procedure, monitors the safety of medicines across their lifecycle and provides information to healthcare professionals and patients.

   Medicines | European Medicines Agency

   www.ema.europa.eu/en/medicines

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   What medicines are included in EMA's work?

   • The medicines included in our work include medicines for human use, medicines for veterinary use and herbal medicines. You can dowload EMA's medicine-related data published on this website in Excel table format

   Medicines | European Medicines Agency

   www.ema.europa.eu/en/medicines

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   What does the European Medicines Agency do?

   • 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). The Agency's main responsibilities are authorising and monitoring medicines in the EU.

   European Medicines Agency – EMA | European Union

   european-union.europa.eu/institutions-law-budget/institutions-and-bodies/search-all-eu-institutions-and-bodies/european-medicines-agency-ema_en

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   How do I find authorised medicines?

   • 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).

   Medicines | European Medicines Agency

   www.ema.europa.eu/en/medicines

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