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ISO 15189:2022 Clinical Laboratory Accreditation Standard Requirements

ISO 15189:2022 Clinical Laboratory Accreditation Requirements

ISO 15189:2022 Clinical Laboratory Accreditation Requirements 18 & 19/06/2025 14 hours Limassol Approved by HRDA   Description of the training program The implementation of the accreditation standard for clinical laboratories CYS EN ISO 15189 has proven to contribute effectively to the internal organization of the clinical laboratory, to the better management of patients' needs and the enhancement of their satisfaction, to ensure the reliability of results and to the preparation for reception of the General Health System. It is necessary to inform the clinical laboratory managers and all executives related to the effective operation of the laboratory, about the requirements and philosophy of the new ISO 15189:2022 standard so that its subsequent effective implementation is possible. The aim of the program is therefore to cover the basic concepts and requirements of the standard CYS EN ISO 15189:2022, and to provide specialized knowledge on individual issues related to accreditation and useful tips for the practical application of the standard.   The topics...

March 6, 2025
Health care, Multi-Business
Risk Assessment in Clinical Laboratory- from theory to practice

Risk Assessment in the Clinical Laboratory -from theory to practice

Risk Assessment in the Clinical Laboratory -from theory to practice 06/05/2025 13/05/2025 14 hours Limassol 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...

March 6, 2025
Health care, Multi-Business
External Quality Control in Clinical Laboratory

External Quality Control in Clinical Laboratory

External Quality Control in Clinical Laboratory 18/03/2025 7 hours Limassol Approved by HRDA   Description of the training program External Quality Control in clinical laboratories, is applied to an external standard by an external body and is based on the results of sample analysis at regular intervals by many laboratories. It is an effective way to monitor the performance of the laboratory and check the validity of the overall quality system. The identification and taking of corrective measures to avoid or eliminate errors in external quality control is a daily occupation of the scientific staff of the laboratories. The purpose of our training program is to inform participants about the necessity of implementing and evaluating the results of External Quality Control and therefore to provide them with specialized knowledge and useful information for identifying and taking corrective and preventive actions and monitoring their effectiveness.    The topics of the training program is ideal for: Laboratory Directors of Clinical Laboratories Supervisory Executives...

March 3, 2025
Health care, Home page news, Multi-Business
INTERNAL QUALITY CONTROL IN THE CLINICAL LABORATORY

Internal Quality Control in Clinical Laboratory

Internal Quality Control in clinical Laboratory 07/11/2024 7 hours Limassol Approved by HRDA   Description of the training program Internal quality control is applied daily by the clinical laboratory and aims to certify the repeatability and accuracy of the method against an internal standard. The results of these audits are statistically processed using various methods to identify errors in real time and take corrective action. The identification and taking of corrective measures to avoid or eliminate errors in internal quality control is a daily occupation of the scientific staff of the laboratories. The purpose of our training program is to inform participants about the necessity of implementing and evaluating the results of Internal Quality Control and therefore to provide them with specialized knowledge and useful information for identifying and taking corrective, preventive actions and monitoring their effectiveness.    The topics of the training program is ideal for: Laboratory Directors of clinical laboratories Supervisory Executives of Clinical Laboratories Clinical Laboratory Officers e.g....

October 1, 2024
Health care, Multi-Business
ISO 15189:2022 Clinical Laboratory Accreditation Standard Requirements

ISO 15189:2022 Clinical Laboratory Accreditation Standard Requirements

ISO 15189:2022 Clinical Laboratory Accreditation Standard Requirements 09 & 12/12/2024 14 hours Limassol Approved by HRDA   Description of the training program The implementation of the accreditation standard for clinical laboratories CYS EN ISO 15189 has proven to contribute effectively to the internal organization of the clinical laboratory, to the better management of patients' needs and the enhancement of their satisfaction, to ensure the reliability of results and to the preparation for reception of the General Health System. It is necessary to inform the clinical laboratory managers and all executives related to the effective operation of the laboratory, about the requirements and philosophy of the new ISO 15189:2022 standard so that its subsequent effective implementation is possible. The aim of the program is therefore to cover the basic concepts and requirements of the standard CYS EN ISO 15189:2022, and to provide specialized knowledge on individual issues related to accreditation and useful tips for the practical application of the standard.   The...

September 9, 2024
Health care, Home page news, Multi-Business
External Quality Control in Clinical Laboratory

External Quality Control in Clinical Laboratory

External Quality Control in Clinical Laboratory 21/11/2024 7 hours Limassol Approved by HRDA   Description of the training program External Quality Control in clinical laboratories, is applied to an external standard by an external body and is based on the results of sample analysis at regular intervals by many laboratories. It is an effective way to monitor the performance of the laboratory and check the validity of the overall quality system. The identification and taking of corrective measures to avoid or eliminate errors in external quality control is a daily occupation of the scientific staff of the laboratories. The purpose of our training program is to inform participants about the necessity of implementing and evaluating the results of External Quality Control and therefore to provide them with specialized knowledge and useful information for identifying and taking corrective and preventive actions and monitoring their effectiveness.    The topics of the training program is ideal for: Laboratory Directors of Clinical Laboratories Supervisory Executives...

August 2, 2024
Health care, Home page news, Multi-Business
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