№ files_lp_3_process_9_37629
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Step-by-step procedural guide for ABO and Rh(D) blood typing including specimen preparation, reagent handling, testing on the Immucor Galileo Echo, quality control measures, result validation, and reporting.
Year: 2026
Region / City: Laboratory / Clinical Setting
Subject: Blood group typing and donor unit confirmation
Document Type: Laboratory Procedure Manual
Organization / Institution: Immucor Laboratories
Author: Laboratory Standards Committee
Target Audience: Laboratory technologists and blood bank staff
Applicable Period: Ongoing standard operating procedure
Approval Date: 2026-01-15
Equipment: Immucor Galileo Echo
Reagents: Anti-A series 1, Anti-B series 3, Anti-D series 4, Monoclonal control, CMT strips, PHIX buffered saline
Specimen Requirements: Single segment from donor unit, spin and wash if hemolysed
Quality Control: Daily commercial QC using WB corQC, valid results allow subsequent testing within 24-hour interval
Reporting System: LIS (Cerner)
Price: 8 / 10 USD
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Principle for Resolving ABO Grouping Discrepancies
Note: Year
Theme: Blood Transfusion, ABO Grouping
Document Type: Procedure
Target Audience: Medical Laboratory Staff
Dr. Adnan Abo Alhaija's Academic and Professional Background
Year: 2018–present
Region / City: Riyadh, Saudi Arabia
Topic: Academic Background, Professional Experience, Finance
Document Type: Biography
Institution: Alfaisal University, King Saud University, Bowling Green State University
Author: Dr. Adnan Abo Alhaija
Target Audience: Academic professionals, students in economics and business
Period of Activity: 2010–present
Date of Approval: N/A
Date of Changes: N/A
Principle Maintenance for Immucor Galileo Echo Instrument
Year: N/A
Region / City: N/A
Subject: Instrument Maintenance
Document Type: Protocol
Organization / Institution: N/A
Author: N/A
Target Audience: N/A
Effective Period: N/A
Approval Date: N/A
Amendment Date: N/A
Maintenance Procedure for Immucor Galileo NEO Instrument
Year: N/A
Region / City: N/A
Subject: Maintenance
Document Type: Procedure
Organization / Institution: Immucor
Author: N/A
Target Audience: Administrative user, MLT 3, NEO key operator
Validity Period: N/A
Approval Date: N/A
Amendment Date: N/A
IgG Antibody Panel Testing Procedure on Immucor Galileo Echo
Instrument: Immucor Galileo Echo
Test Panels: Capture-R Ready-ID; Capture-R Extend I; Capture-R Extend II
Test Method: IgG antibody panel using Capture-R technology
Temperature: 37°C
Specimen Type: EDTA anticoagulated whole blood; serum from fully clotted blood
Specimen Stability: ≤5 days from collection; ≤4 days for recently transfused or pregnant patients
Exclusion Criteria: Hemolyzed (≥3+), lipemic, or icteric samples not accepted
Reagents: Capture LISS; Capture-R Ready-ID; Capture-R Extend I & Extend II; Capture-R Indicator Cells; WB corQC; PHIX buffered saline
Equipment: Immucor Galileo Echo
Quality Control: Commercial WB corQC performed daily; 24-hour control interval after validation
Controls: Positive and negative controls included in each 14-cell panel
Related Policy: SWIM manual NRT.007 “Antibody Identification of Warm Reactive Antibodies”
Reporting: Results reviewed and confirmed by technologist; specimens forwarded for additional antibody testing if required
Restrictions: Partially used strips cannot be reused
References: Galileo Echo Operator Manual; SWIM manual
Topics: RhD ABO Immucor