Updated April 13, 2021
The original links broke.
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An Introduction to FDA's Regulation of Medical Devices - FDA.gov
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According to the FDA, the quality system regulation includes requirements related to the methods used in and the facilities and controls used for: designing, purchasing, manufacturing, packaging, labeling, storing, installing and servicing of medical devices. Manufacturing facilities undergo FDA inspections to assure compliance with the QS requirements.
Checkout this free training offering by the FDA, Quality System Regulation 21 CFR Part 820 Basic Introduction (video).
Here's what you get with the complete course offering:
- Quality System Regulation 21 CFR Part 820 Basic Introduction - Online Video Presentation (with Captioning)
- Quality System Regulation 21 CFR Part 820 Basic Introduction - Printable Slide Presentation
You might also be interested in:
Essentials for Medical Device Manufacturers - a training class by SkillsPlus International Inc.
Teaches employees the essential elements of QSR for beginning work in the medical device industry
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If you are looking for live, onsite, in-person delivered courses or classes, then consider the following popular courses:
SkillsPlus Intl Inc. - The best GMP training, best QSR training, best instructors
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