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EU Medicines Agency
Latest news from the European Medicines Agency, the European Union agency responsible for the evaluation and supervision of medicines. RTs ≠ endorsement.
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EU Medicines Agency Jun 24
Check out the agenda of this week’s meeting of the Committee for Human ():
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EU Medicines Agency Jun 24
Only one week left to share your ideas and suggestions with us on EMA's Regulatory Science Strategy to 2025. Your feedback is very important to help us ensure a thorough assessment of ground-breaking, more complex therapies. 👉
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EU Medicines Agency retweeted
ECDC Jun 19
Infants and children are often believed to be the only age group affected by , but the disease can be contracted at any age. Check your status. Latest measles data:
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EU Medicines Agency retweeted
EU_Health Jun 18
Are you a health professional communicating about ? Help address misconceptions by following 's tips: 1. emphasise facts and display them graphically 2. pay attention to language 3. use warnings if information is false
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EU Medicines Agency Jun 18
Today we are meeting EU healthcare payers in Diemen 🇳🇱 to discuss evidence generation for , unmet medical needs & horizon scanning for . Our close collaboration is key for timely & affordable access for to new 💊💊 👉
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EU Medicines Agency Jun 17
What are the highlights of EMA’s Management Board meeting in June 2019?
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EU Medicines Agency Jun 17
What should regulators do to keep pace with scientific advances in medicine 💊development? We want to hear your suggestions. 👉
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EU Medicines Agency Jun 14
What happened during the June meeting of EMA's committee ? The PRAC started a review of medicines. 👉
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EU Medicines Agency Jun 12
How can the regulatory system better address the challenges faced by due to scientific progress? Share your ideas 💡with us: 👉
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EU Medicines Agency Jun 11
What's on the agenda of our committee () meeting in June?
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EU Medicines Agency Jun 11
Two additional countries to benefit from EU-US mutual recognition agreement for inspections:
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EU Medicines Agency Jun 6
Views and input from and will be more easily incorporated into the Agency’s activities. 👉
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EU Medicines Agency Jun 6
EMA will gain a better understanding of how medicines 💊 are being used in real life, for the benefit of . 👉
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EU Medicines Agency Jun 6
How many recommendations for eligibility to EMA's PRIME scheme were granted in May? Follow for the latest updates. 👉
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EU Medicines Agency Jun 6
Today we've signed 🖊️ a joint statement with , & to strengthen our interaction with GPs and . Close collaboration helps us understand better the needs of . 👉
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EU Medicines Agency Jun 5
that EMA provides support to to navigate the regulatory processes related to the development and the authorisation of ? See the annual report 2018 for EMA's SME Office. 👉
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EU Medicines Agency Jun 4
DYK that , the EU Member States and companies are responsible for detecting and managing safety signals? A safety signal is an information on a that may be caused by a 💊 and requires further investigation. 👉
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EU Medicines Agency Jun 3
EMA has released a draft guideline on the quality requirements for medical devices in human medicines that include a medical device, known as drug-device combinations, for a 3-month public consultation. 👉
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EU Medicines Agency Jun 3
The EMA "Regulatory Science to 2025" strategy covers 💊for both human and animal use 🐮🐷🐶. See what the strategy aims to achieve in medicine:
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EU Medicines Agency May 29
EMA’s human medicines committee () recommends 4 for approval at its May 2019 meeting:
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