The European Blood Alliance, representing public/not-for-profit blood establishments, welcomes the European Commissions publication of its proposal for a reform of the EU pharmaceutical legislation. The review aims to reach a number of important goals, such as improving access to innovative medicines, promoting innovation in the sector and addressing shortages.
European Blood Alliance (EBA)
NGO · Belgium · EU Transparency Register 149855010621-40
Counts here are a floor, never a total: they cover the 665 consultation files tracked so far (57,774 submissions, mostly 2021–26), so an organization's real filing history is larger, not smaller.
Who they are
Among the 1106 non-governmental organisations on this site, they rank #255 by legislative files engaged, a count of participation, not a measure of influence.
Declares membership of
- Common representation of Substances of Human Origin (SoHO)
- https://europeanbloodalliance.eu/european-affairs/core-soho/
- Alliance of Blood Operators (ABO: https://www.allianceofbloodoperators.org/)
- Coalition of Blood for Africa (CoBA: https://cobaafrica.org/)
- International Society of Blood Transfusion (ISBT: https://www.isbtweb.org/)
- International Plasma and Fractionation Association (IPFA: https://ipfa.nl/)
Self-declared to the EU Transparency Register (snapshot 14 Oct 2026).
- Register category
- Non-governmental organisations
- Registered as
- European Blood Alliance (EBA)
- Head office
- Amsterdam, Netherlands
- EU office
- Brussels
Self-declared to the EU Transparency Register (snapshot 14 Oct 2026); cost bands are floors, not audited totals. Reused under Commission Decision 2011/833/EU.
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Their record over time
European Blood Alliance (EBA) filed 6 positions between 14 Dec 2020 and 30 Mar 2026, across 5 of the 665 legislative files tracked here, attaching a full position paper 3 times.
What they argued
The European Blood Alliance (EBA), representing public and non-profit blood establishments across Europe, welcomes the European Commissions proposal for a European Biotech Act. EBA wishes to remind EU and national policymakers that public and non-profit blood establishments are the original precursors of personalised medicine and have played an historic and central role in the development of many ground-breaking…
The European Blood Alliance (EBA) welcomes this proposal on the European Health Data Space (EHDS). European blood establishments represented by EBA have regularly asked for more and better data to increase donor protection and reinforce patient care; we believe that the EHDS can be a fundamental tool in working towards these goals.
The European Blood Alliance, representing public/not-for-profit blood establishments, welcomes the European Commission’s proposal for a SoHO Regulation and is pleased with the general direction of the proposal and its level of ambition.
EBA agrees with the gaps and issues identified in the 1st part of the IIA and highlights the following: Reliance on 3rd countries on plasma for PDMPs is in part due to off-label non-evidence-based use.The EU needs to support more research on efficacy of the plasma-based products for a number of diseases while Member States (MS) need to increase their plasma collection from the not-for-profit sector EBA strongly…
The European Blood Alliance (EBA, www.europeanbloodalliance.eu) welcomes the proposal for a European Medicines Agency (EMA) increased role in crises preparedness and management of Plasma-Derived Medicinal Products (PDMPs) supply.
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Turns up on the same files
Organizations that also filed on at least two of the same consultations. A shared interest in the same dossiers, not evidence of coordination, and we do not suggest any.
Showing 5 of 117.
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Everything on this page comes from European Blood Alliance (EBA)’s own submissions to the European Commission. We have added nothing and interpreted nothing. If something is wrong or out of date, email info@policyspeak.com and we will correct it. If you are an individual named in a record, our privacy policy sets out your rights to correction, objection and removal.
Quotes are verbatim from submissions published by the European Commission, trimmed to their opening passage and never summarized by a model. Organizations only, never individuals. Reused under Commission Decision 2011/833/EU; the European Commission is not liable for this reuse.