CLSI EP23 IQCP
EP23 IQCP: Quality Control Based on Risk Management
The EP23™ IQCP: Quality Control Based on Risk Management course imparts the knowledge and skills necessary for the successful implementation of an individualized quality control plan (IQCP) based on the document CLSI EP23, Laboratory Quality Control Based on Risk Management. This on-demand course is designed to be accessible to anyone, anywhere, and at any time, making it a valuable resource for laboratory technicians, quality managers, and health care professionals. By the end of the course, you'll be equipped with the tools and insights needed to effectively apply risk management principles to your quality control processes, ensuring higher standards of accuracy and reliability in your laboratory.
Please e-mail customer service at customerservice@clsi.org for group registration requests for your organization.
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Free
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After participating in this course, learners will be able to:
- Review the CLIA IQCP requirements.
- Provide an overview of risk management.
- Apply risk management to laboratory testing.
- Create a quality control plan (QCP).
Course Modules
Module 1: Introduction to EP23 and IQCP
Module 2: CMS and CLIA Requirements for Laboratories Implementing IQCPs
Module 3: Introduction to Risk Assessment
Module 4: US CLIA Requirements for the Risk Assessment
Module 5: Performing the Risk Assessment
Module 6: Assembling the Quality Control Plan
Module 7: The Quality Assessment
Module 8: Summarizing IQCP
Intermediate: Refresher course. Some basic knowledge required, for the experienced staff technologist with some years of experience.
CLSI is approved as a provider of continuing education programs in the clinical laboratory sciences by the ASCLS P.A.C.E.® Program.
Learning Objectives
After participating in this course, learners will be able to:
- Review the CLIA IQCP requirements.
- Provide an overview of risk management.
- Apply risk management to laboratory testing.
- Create a quality control plan (QCP).
Course Modules
Module 1: Introduction to EP23 and IQCP
Module 2: CMS and CLIA Requirements for Laboratories Implementing IQCPs
Module 3: Introduction to Risk Assessment
Module 4: US CLIA Requirements for the Risk Assessment
Module 5: Performing the Risk Assessment
Module 6: Assembling the Quality Control Plan
Module 7: The Quality Assessment
Module 8: Summarizing IQCP
Intermediate: Refresher course. Some basic knowledge required, for the experienced staff technologist with some years of experience.
CLSI is approved as a provider of continuing education programs in the clinical laboratory sciences by the ASCLS P.A.C.E.® Program.