EBA concerned with rules on medical devices and in vitro diagnostics
The European Blood Alliance responded to the European Commission’s target evaluation of Regulations 2017/745 and 2017/746 on medical devices and[…]
The European Blood Alliance responded to the European Commission’s target evaluation of Regulations 2017/745 and 2017/746 on medical devices and[…]
Regulation (EU) 2024/1938 on standards of quality and safety for substances of human origin intended for human application (SoHO Regulation)[…]
We are pleased to share the highlights from our recent webinar on the applications and advancements of human platelet lysate,[…]
Today the world commemorates the 20th World Blood Donor Day under the motto “20 years of celebrating giving: Thank you,[…]
Brussels, 24 April 2024 Peter O’Leary, EBA Executive Director, said “the text adopted today is a historic step forward for[…]
Blood donation eligibility policies for men who have sex with men (MSM) have evolved since they were found to be[…]
CoRe SoHO statement on hierarchy of guidelines concerning protection of SoHO donors, recipients, and offspring As the trilogue meetings on[…]
Joint statement of EBA and IFBDO/FIODS on voluntary non-remunerated donations (VNRD) in the context of the negotiations of the future SoHO[…]
EBA is pleased to announce the inaugural edition of the SUPPLY Project Newsletter. Plasma and plasma-derived medicinal products play an[…]
17 October 2023 General Position on the European Commission’s proposal for a reform of the EU pharmaceutical legislation The European[…]