FDA 21 CFR 820 cGMP - 2024 Overview
This 1-hour e-course is an annual GMP Overview of the Quality System Regulations (QSR) and FDA 21 CFR 820 GMP requirements for Medical Devices. Includes a certified training Certificate of Competence. 0.1 CEUs.
Course Curriculum
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How to use this course
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FDA 21 CFR 820 cGMP Overview_Lesson-01
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FDA 21 CFR 820 CGMP Overview_Lesson-01-QUIZ
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FDA 21 CFR 820 cGMP Overview_Lesson-02
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FDA 21 CFR 820 CGMP Overview_Lesson-02-QUIZ
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FDA 21 CFR 820 cGMP Overview_Lesson-03
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FDA 21 CFR 820 CGMP Overview_Lesson-03-QUIZ
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Video-Congratulations-Next Steps
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FDA 21 CFR 820 cGMP | 2024 Overview
- $295.00
- On Demand / Student-Paced
- 1 hour / 0.1 CEUs
- English
- Certified Training
Learning Objectives
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Understand key concepts and major requirements of the FDA 21 CFR Part 820 Quality System Regulations
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Know roles and responsibilities to support CGMP compliance
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