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Medical Devices

QS Regulation 7: Corrective and Preventive Action

About the Course

This seventh in a series of Quality System (QS) Regulation elearning courses targets Corrective and Preventive Action (21 CFR Part 820 Subpart J). Topics include: Key Terms, Investigate and Identify, Changes, Information, and Analyzing Data. After completing this online learning course, you will be familiar with a manufacturer’s responsibilities relative to the corrective and preventive action requirements of the QS Regulation. Learners should complete the previous courses in the series before taking this course.