French Public Health Code
In forceI.-Each blood establishment is required to collect and keep, for each unit of labile blood product which it prepares, the following information:
1° The identification of the donation of blood or blood components from which the unit was obtained and the identification of the donor ;
2° The results of the biological analyses and screening tests carried out on the donation;
3° The identification of the blood establishment to which the prepared unit was sent, when the unit was distributed to another blood establishment.
II - Each blood establishment is required to collect and keep, for each unit of labile blood products which it distributes or issues, the following information:
1° Identification of the health establishment to which units of labile blood products have been distributed or issued and, when a health establishment issues a labile blood product for a patient hospitalised in another health establishment, the circumstances of this issue and the identification of the latter ;
2° The identification of the prescriber and the identification of the patient to whom the unit was administered or, where applicable, the date on which the unit was destroyed or returned to the blood establishment.
III - Each blood establishment sends the National Public Health Agency the data required for epidemiological monitoring of blood donors and candidates for scheduled autologous transfusion.
