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Dear all,
as Gaia wrote before I think it would be better to split the “Risk Mitigation” subject into two sub-sections.
1) Risk Mitigation for adverse reactions in donors – Physical requirements (age, gender, et al) and DHQ
2) Risk Mitigation for adverse reactions in recipients – DHQ, screening lab tests for donors; viral inactivation and quality controls/bacterial contamination; need to standardize hemo and bio-vigilance systems.