QS Regulation 7: Corrective and Preventive Action
The seventh in a series of Quality System (QS) Regulation courses, this course focuses on Corrective and Preventive Action (21 CFR Part 820 Subpart J). The QS Regulation provides a framework of basic requirements for manufacturers of finished medical devices. Topics include: Key Terms, Investigate and Identify, Changes, Information, and Analyzing Data. After completing this 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.
After this course learners will be able to identify a manufacturer’s responsibilities relative to the corrective and preventive action requirements of the qs regulation.