QSIT 4 -- The Corrective and Preventive Actions Subsystem

This is the fourth in a series of courses designed to instruct on the Quality System Inspection Technique (QSIT). The series provides guidance for inspecting medical device manufacturers against the Quality System Regulation, 21 CFR Part 820. Topics in this course include: Procedures, Problems, Received Data, Failure Investigations, Actions, and Documentation and Communications. After completing this course, learners will be able to identify the ten inspectional objectives associated with the CAPA subsystem and recognize the ways to accomplish those inspectional objectives.

After this course learners will be able to identify the ten inspectional objectives associated with the capa subsystem and recognize the ways to accomplish those inspectional objectives.