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Updated: Jun 28, 2026
12:40
Preparation and Pathogen Inactivation of Double Dose Buffy Coat Platelet Products using the INTERCEPT Blood System
Published on: December 7, 2012
[Conditions for blood components return, after storage in a depot]
1Laboratoire de biologie, CHI Elbeuf-Louviers-Val-de-Reuil, Elbeuf, France. isabelle.herve@chi-elbeuf-louviers.fr
Summary
The Etablissement français du sang (EFS) can now re-introduce returned blood components. This requires collaboration between EFS and health facilities to ensure optimal transport and storage conditions using electronic temperature monitors.
Area of Science:
- Transfusion Medicine
- Biologistics Management
- Quality Control in Healthcare
Context:
- Regulatory changes permit the reintroduction of returned blood components into EFS stock.
- This process involves shared responsibility between EFS and healthcare facilities.
- Effective collaboration is crucial for maintaining blood component integrity.
Purpose:
- To outline an organizational framework for managing returned blood components.
- To establish necessary procedures for checking the return process.
- To implement a method for tracking transportation conditions.
Summary:
- The article details an organizational strategy for managing returned blood components.
- It emphasizes the need for collaboration between EFS and health establishments.
- The proposed system utilizes electronic temperature monitors to track conditions during transport and storage.
Impact:
- Ensures the quality and safety of blood components throughout the supply chain.
- Facilitates compliance with new regulations for blood component management.
- Enhances the efficiency and reliability of blood product logistics.
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