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The fifth EMA-Nuclear Medicines Europe bilateral meeting is organised in the context of the EMA annual bilateral meetings with industry stakeholder organisations.
EMA’s emergency task force (ETF) organises meeting with experts and stakeholders to strengthen knowledge on biodistribution of mRNA vaccine components
The European Medicines Agency publishes the recommendations by the Committee for Veterinary Medicinal Products (CVMP) under the limited market provisions of the Veterinary Medicinal Products Regulation. These include classifications on limited market according to Article 4(29) and eligibility under Article 23.
Each month, the European Medicines Agency publishes an overview listing all safety signals discussed during the latest Pharmacovigilance Risk Assessment Committee (PRAC) meeting and the recommendations given for each of them. The overview includes PRAC recommendations for centrally and nationally authorised medicines.