EU Medicines AgencyVerified account

@EMA_News

Latest news from the European Medicines Agency, the European Union agency responsible for the evaluation and supervision of medicines. RTs ≠ endorsement.

Joined February 2010

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  1. Dec 11

    Send us comments! We will address as many as possible after the meeting, and our responses will be published on EMA’s website.

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  2. Dec 11

    After authorisation, EMA is urging citizens not to get from unauthorised websites & vendors aiming to exploit fears during . Citizens should follow official vaccination programmes rather than seeking out alternative sources of vaccines.

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  3. Dec 11

    EMA talks to and doctors, pharmacists and nurses, in EMA’s pandemic task force, in regular meetings and to test information materials.

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  4. Dec 11

    Check EMA’s information about: ➡️how are being developed, approved & monitored ➡️studies needed for the approval of these vaccines in the EU.

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  5. Dec 11

    Once a is authorised in the 🇪🇺, EMA will publish: ➡️Product info ➡️Summary of assessment in lay language ➡️European Public Assessment Report ➡️Full risk management plan ➡️Clinical data supporting authorisation ➡️Regular safety updates

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  6. Dec 11

    EMA will provide an unprecedented level of transparency and data access for all medicines. Find out more about EMA’s communication and increased transparency measures in this presentation:

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  7. Dec 11
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  8. Dec 11

    safety gets stronger with your participation! Patients and healthcare professionals play a critical role in reporting suspected side effects.

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  9. Dec 11

    Established side effects detected during with will be included in the package leaflet that is available to .

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  10. Dec 11

    EMA has a detailed plan to monitor safety in practice and to act immediately to protect the health of EU citizens:

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  11. Dec 11
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  12. Dec 11

    The 🇪🇺 has a strict and robust safety monitoring system to ensure vaccines’ benefits are always higher than any potential risk.

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  13. Dec 11
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  14. Dec 11

    development and evaluation are compressed in time, but they will be approved according to the same high standards that apply to all 💊 in the 🇪🇺.

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  15. Dec 11

    Views received during the public meeting will be shared with EMA and its experts and will be taken into consideration during the evaluation and continued monitoring of .

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  16. Dec 11

    Follow our Twitter posts during the COVID-19 vaccines public meeting, by using the hashtag .

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  17. Dec 11

    We are starting the public meeting on . Join us to learn more of the EU scientific evaluation for and to hear the voice of people on this subject:

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  18. Dec 11
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  19. Dec 11
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  20. Europe already has a robust system to ensure long-term vaccine safety. The European Medicines Agency has a solid track record in keeping Europe safe. constantly monitors medicines’ safety and exchanges information at global level.

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