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Mastering CBAHI Standards:Simple & Easy
Mastering CBAHI Standards:Simple & Easy
Curriculum
16 Sections
87 Lessons
Lifetime
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Alfa Media PDF Library -المكتبة المركزيه للمعايير
1
1.1
المكتبة المركزيه
I. Organization
8
2.1
01100-Organization Chart Structure
2.2
01200- Scope of Service
2.3
01300 – Mission, Vision and Values
2.4
01400-Strategic Plan
2.5
01500-Quality Managment Programm
2.6
01600 – Deviations and Exceptions Control
2.7
01700-Communication of Concerns
2.8
01800 – Emergency preparedness/Disaster Plan
II. Customer Focus
4
3.1
02100- Identification of Customer Needs
3.2
02300- Agreements with Clinical Services
3.3
02400 – Turned Around Time
3.4
02500-Direct to Patient Customer Testing
III. Facility and Safety
6
4.1
03100-Design, Accessibility and Space Allocation
4.2
03200 -Work Environment Facilities and Maintenance
4.3
03300 – Safety Manual
4.4
03400- Safety training
4.5
03450 -Risk Management
4.6
03500- Mointring of Safety Programm
IV.Personeel
12
5.1
04100-Employment and Retention
5.2
04150 -Governance Responsabilties
5.3
04200-Qualifications and Responsibilities of the Laboratory Medical Director
5.4
04300 -Qualifications and Responsibilities of All Personnel
5.5
04400-Qualifications and Responsibilities of Portfolio Holders
5.6
04500 Delegation of Functions/ Authority
5.7
04550-Credentialing
5.8
04575- Privileging
5.9
04600- Training & Orientation
5.10
04700- Competency Assessment
5.11
04800- Continuing Education and Professional Development
5.12
04900 – Personnel Records
V. Purchasing and Inventory
6
6.1
05100 – Identification of Critical Reagents, Supplies and Services
6.2
05200 – Supplier Issues
6.3
05300 – Reference Laboratory Services
6.4
05400 – Receipt, Inspection and Testing of Critical Supplies and Services
6.5
05500 – Storage, Inventory Management and Tracking of Critical Materials
6.6
05600 – Labeling of Reagents and Solutions
VI. Equipment
10
7.1
06050 -Identification of Critical Equipment
7.2
06150 – Validation of Critical Equipment
7.3
06100 – Receipt, Inspection and Testing of Critical Equipment
7.4
06200 – Equipment Monitoring, Maintenance and Repairs
7.5
06300 – Monitoring of Blood and Blood Components Storage Devices
7.6
06350 -Transportaion of Blood & Blood Components
7.7
06400 – Reagents and Supplies Storage Devices
7.8
06450 -Calibration and Standardization
7.9
06550 – Investigation and Follow-up of Critical Equipment Failure
7.10
06600 – Critical Equipment Records
VII.A.Process Management – General Laboratory
7
8.1
07110 – Change Control (New/Revised Process)
8.2
07120 -Traceability
8.3
07130 – Personnel Audit Trail
8.4
07140 -Method Validation
8.5
07150 -Quality Control-General Requirements
8.6
07160 -Definition and Quality Control of Water Types
8.7
07180 – Instruments/ Methods Correlation
VII.B.Process Management-Specimen and Request
8
9.1
07210 – Specimen Collection and Service Manual
9.2
07220 – Labeling of Specimen Container
9.3
07230 – Handling and transportation of Specimen
9.4
07240 – Receipt and Inspection of Specimen
9.5
07250 – Test, Product and Services Requests
9.6
07260 – Monitoring Misidentification Risks
9.7
07270 – Acceptance of Suboptimal Specimen
9.8
07280 – Specimen Retention
VII.C.Process Management-Results Reporting
4
10.1
07710 – Results Reporting
10.2
07720 – Critical Results Reporting
10.3
07730 – Corrected/Amended Reports
10.4
07750 – Reference Ranges and Cut-off Values
VIII. Documents and Records
5
11.1
08100- Document Control/Management System
11.2
08200- Procedure Manuals and Work Instructions
11.3
08300- Records Control/Management System
11.4
08400 – Correcting/Changing Records
11.5
08500- Documents and Records Retention System
IX. Information Management
9
12.1
09100 – Computer System Policies (Confidentiality, Access andSecurity)
12.2
09200 – Computer System Validation
12.3
09300 – Technical Support
12.4
09400 – Operating Manual
12.5
09500 – Computer System Modifications and Updates
12.6
09600 – Data Integrity
12.7
09700 – Downtime and Alternative System
12.8
09800 – Data Backup and Restoration
12.9
09900-Computer System Maintenance
X.Nonconforming Event Management
1
13.1
10100 – Nonconforming Events Policy and Procedure
XI. Assessments
4
14.1
11100 – Internal Assessment
14.2
11200 – External Assessment (Surveys and Inspections)
14.3
11300-Proficiency Testing
14.4
11400 – Quality Indicators
XII. Continual Improvement
1
15.1
12100 – Process Improvement
FAQ اسئلة متكررة
1
16.1
FAQ related CBAHI Standrds
01100-Organization Chart Structure
شاهد هنا
https://academy.alfalab.sa/wp-content/uploads/2025/01/01100.mp4
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