Medical Device Packaging, Labeling, and Distribution

Mistakes or mix-ups in the critical areas of product packaging, labeling, and distribution can pose a danger to the consumer. This course provides you with information on current packaging and labeling requirements specified by the Quality System Regulation. A basic understanding of quality system regulations for medical device and equipment manufacturers (21 CFR 820), quality control procedures, and quality principles are prerequisites for this course. Topics in this course include: Importance of Labeling, Packaging, Label Control, and Distribution. After completing this course, learners will be able to recognize the requirements for packaging, labeling, and distribution of medical devices 21 CFR 820.120-160.