Risk Assessment in the Clinical Laboratory is very essential to be understood and applied from theory to practice. Labs should reconfigure their procedures to an extent that meets the requirements of the standard ISO15189 with the goal of achieving accreditation. A requirement of the standard ISO15189 is the assessment of risks to the clinical laboratory, which may have negative effects on both the quality of health services and the reliability of the results provided to laboratory users.
The program aims to train clinical laboratory executives in risk management in accordance with the ISO 22367:2020 standard, with the aim of complying with the requirements of ISO 15189 and achieving accreditation. It focuses on identifying, assessing, and mitigating risks that affect the quality of services and the reliability of outcomes, enhancing patient safety and experience.
The training program is ideal for:
- Laboratory Directors of Clinical Laboratories
- Supervisory Executives of Clinical Laboratories
- Clinical Laboratory Officers e.g. medical laboratory technologists, biomedical scientists, biologists, chemists, etc.
- Internal Auditors of Clinical Laboratories
- Quality Managers of Clinical Laboratories
- Company Management Systems Managers and
- Executives of companies providing services and products to the Laboratories e.g. analyzer maintenance technicians, reagent companies and representatives of external quality control bodies
Our experienced Instructor will provide all the necessary information and knowledge to the participants.
If you are interested in the specific subsidized training program, contact us
