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| Testing | |
|---|---|
The physical and medical exam at donor work up is performed by a medical doctor: | YES / NO |
| All donor testing (at work up) for infectious disease is performed in a laboratory certified/licensed by a Competent Authority: | YES / NO |
| HLA typing for patient specific request is performed in an appropriately accredited laboratory: | YES / NO |
| Sterility testing is performed on the adult donor product: | YES / NO |
| Sterility testing is performed on the cord blood product: | YES / NO |
Reporting of Serious Adverse Events Please indicate which of the following schemes for reporting Serious Adverse Events relating to either the Donor or the product the Registry participates in: | Additional comments | |
| Mandatory National Reporting Scheme | YES / NO | |
Voluntary National Reporting Scheme | YES / NO | |
WMDA SEAR/SPEAR Reporting Scheme: | YES / NO | |
| The Registry will notify the receiving Registry within 24 hours of receiving information relating to any serious adverse event that could be considered to affect the patient receiving the product? | YES / NO |
| Retention policy | |
|---|---|
| Donor records relating to the medical and HPC collection process are retained for: |
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