QS Regulation 6: Acceptance Activities; Nonconforming Product
<p>The sixth in a series of Quality System (QS) Regulation courses, this course focuses on Acceptance Activities (21 CFR Part 820 Subpart H) and Nonconforming Product (21 CFR Part 820 Subpart I). The QS Regulation provides a framework of basic requirements for manufacturers of finished medical devices.</p>
After this course learners will be able to recognize a manufacturer’s responsibilities relative to the receiving, in-process, and finished device acceptance. identify the acceptance status and nonconforming product requirements of the quality system regulation.