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21 CFR 820s New Terminology Country-Specific Terms For Medical Device Quality
The proposed revision to the U.S. Quality System Regulation (aka 21 CFR Part 820) takes a giant leap toward harmonization with other major global.
Stephanie gaulding
Pharmatech associates
Device single audit program
System regulation
Cosmetic act
Quality systems regulation
Quality management system regulation
Non powdered surgeon
Medical devices
Quality system regulation amendments
Quality systems inspection technique
Medical device single audit program
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