Risk Assessment in the Clinical Laboratory -from theory to practice
Risk Assessment in the Clinical Laboratory -from theory to practice
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06/05/2025
13/05/2025 |
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14 hours |
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Limassol |
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Approved by HRDA |
Description of the training program
The laboratory is required to reconfigure its 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.
Clinical laboratory executives should be able to identify, evaluate and manage risks by evaluating the effectiveness of existing and additional measures to be taken. Therefore, it is necessary to train those directly or indirectly related to the clinical laboratory in how to manage risks based on ISO 22367:2020, which provides specialized information and techniques on how to identify, analyze and manage risks especially in clinical laboratories so that reducing errors and achieving improvement is a given.
The topics of 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
If you are interested in the specific subsidized training program, contact us