Enumeration:  5.8

Policy:

1. All processing will be in accordance with good manufacturing practices.
2. All testing will follow manufacturer’s recommended testing methods.
3. The specific processing algorithms will be programmed into the Hematos IIG software.
4. Validation of the processing will be performed by Hematos IIG, which will control final ISBT labelling
5. All abnormal results will be reviewed by a transfusion medicine physician.
6. All policies, processes, and procedures must comply with Qatari, HMC, and applicable accreditation standards (i.e. AABB, CAP, and JCI).

References:

1. HMC 1001 Setting Specification, Version 1.5, Hematos IIG, Medinfo
2. Standards for Blood Banks and Transfusion Services, Current Edition, AABB, Bethesda, Maryland, USA