Quality Systems Explained
Medical Device Quality Systems made simple in everyday language. This content is for anyone working in the medical device space. While the main focus may be medical device quality systems; the lessons, examples, and principals are useful in any regulated industry.Subscribe if Medical Devices Quality Systems information is useful to you!
Helping you learn more and understand Quality Systems better! 😊 Medical Device Quality Systems made simple! Compliance made easier to understand. Real Life stories from the Industry!
We will cover the following topics: CAPA, Corrective and Preventive Action ,Corrective Action Preventive Action, Quality Audit, Internal Audit, FDA, FDA 483, Process Validation, Change Control, Design Controls, Management Controls, Risk Management, Purchasing Controls, Supplier Quality, and much more.
About:
Wayne "Aaron" Snyder has been working in the medical device industry for the last 16 years. Check out my Linkedin page for more information.
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Plumbing 21 CFR § 211.48 (Pharma Executive Series #19)
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Ventilation, air filtration, air heating and cooling 21 CFR § 211.46 (Pharma Executive Series #18)
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Lighting § 211.44 (Pharma Executive Series #17)
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Consultants § 211.34 (Pharma Executive Series #14)
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Scope § 211.1 (Pharma Executive Series #10)
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Applicability of current good manufacturing practice regulations 210.2 (Pharma Executive Series #03)
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Current Good Manufacturing Practices (cGMPs) 21 CFR § 21 CFR Part 210 & 211 (Pharma ES #01)
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