| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3819591 | La Presse Médicale | 2015 | 6 Pages |
Abstract
Integrating these evolutions in regulations through the revision of the European Directives on blood and blood components (the review process is expected to be launched in 2015) should enroll them in the long term, for the benefit of patients, donors and all other stakeholders involved in the transfusion chain.
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Authors
Gilles Folléa, Olivier Garraud, Pierre Tiberghien,