A facility that provides transfusion services must document all transfusion-related activity and meet four requirements: a transfusion service agreement, reviewed and approved by the responsible parties, governing procurement, transfer and availability of blood and blood products; continuous provision of prompt ABO grouping, D (Rho) typing, unexpected antibody detection, compatibility testing and laboratory investigation of transfusion reactions through a CLIA-certified laboratory or one CMS accepts as equivalent; storage conditions, including temperature, appropriate to prevent deterioration wherever blood or products are kept outside a monitored refrigerator, with policies for positive identification of the recipient; and procedures to prevent transfusion reactions and to promptly identify, investigate and report reactions to the laboratory and, as appropriate, to federal and State authorities.
The graph holds this control, the 0 it maps to, and the evidence behind each claim, over MCP and REST.