The BRC carries out its activities in compliance with the legislation and regulations in force which prevail for scientific activities carried out with human biological resources. It also ensures respect for persons and undertakes to monitor the consent of donors for the use of samples and associated personal data.

 

Reception of samples -Verification of the data associated with the samples (freeze sheet) -Verification of the presence of patient consent or non-opposition -Verification of non-conformities (deadlines, samplers, etc…)

Quality in the Biobank

• The CRB has been certified since 2011 according to the NF S 96-900 standard. The BRC carries out its activities in compliance with the legislation and regulations in force that prevail over scientific activities carried out with human biological resources. It also ensures respect for individuals and undertakes to monitor donor consent for the use of samples and associated personal data.
• Temperature control and monitoring (-80°)
• Data traceability (TumoroteK®)
• Quality control of derivative products
• Histological controls
• Quality of clinical annotations (data monitoring)