Latest news on Pharmaceuticals from the European Commission
European Commission approves contract with Moderna to ensure access to a potential vaccine
The European Commission approved a sixth contract under the EU Vaccines Strategy, this time with the pharmaceutical company Moderna. The contract provides for the initial purchase of 80 million doses on behalf of all EU Member States, plus an option to request up to a further 80 million doses, to be supplied once a vaccine has proven to be safe and effective against COVID-19.
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European Commission approves contract with CureVac to ensure access to a potential vaccine
Today, the European Commission approved a fifth contract with the European pharmaceutical company CureVac, which provides for the initial purchase of 225 million doses on behalf of all EU Member States, plus an option to request up to a further 180 million doses, to be supplied once a vaccine has proven to be safe and effective against COVID-19.
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European Commission approves contract with BioNTech-Pfizer alliance
Today, the European Commission approved a fourth contract with pharmaceutical companies BioNTech and Pfizer, which provides for the initial purchase of 200 million doses on behalf of all EU Member States, plus an option to request up to a further 100 million doses, to be supplied once a vaccine has proven to be safe and effective against COVID-19.
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European Commission secures EU access to Remdesivir for treatment of COVID-19
Yesterday, the European Commission has signed a contract with the pharmaceutical company Gilead to secure treatment doses of Veklury, the brand name for Remdesivir. Veklury was the first medicine authorised at EU level for treatment of COVID-19. As from early August onwards, and in order to meet immediate needs, batches of Veklury will be made available to Member States and the UK, with the coordination and support of the Commission.
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Reinforced EU/US collaboration on medicines and tobacco
Senior officials from the European Commission (EC), together with the European Medicines Agency (EMA) and the United States Food and Drug Administration (FDA) held their 2018 bilateral meeting in Brussels, Belgium, on 18 and 19 June. The two-day bilateral regulatory dialogue allowed the strategic partners to review their ongoing cooperative initiatives, discuss strategic priorities for the coming years and further strengthen the continuous close collaboration with specific action in the field of pharmaceuticals.
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European Reference Networks: 900 medical teams to connect across Europe for the benefit of patients
On 1 March the newly established European Reference Networks (ERNs) will start their work. ERNs are unique and innovative cross-border cooperation platforms between specialists for the diagnosis and treatment of rare or low prevalence complex diseases.
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Antimicrobial resistance: Commission launches public consultation on new Action Plan
The Commission launches a public consultation on possible activities to include in the new "One Health" Action Plan against antimicrobial resistance (AMR) it plans to adopt by summer 2017. The consultation includes a questionnaire for public administrations and stakeholders and a questionnaire for citizens, to ensure that everyone has their voice heard on how best the Action Plan can support EU countries in the fight against AMR.
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