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Medical Device QSIT Manual with 11, 803, 806, 820 and 821
Medical Device QSIT Manual with 11, 803, 806, 820 and 821
SKU:978-1-935131-10-6
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US FDA Title 21 CFR Parts
Part 11 - Electronic Records/Electronic Signatures (ERES)
Part 803 - Medical Device Reporting
Part 806 - Medical Devices; Reports of Corrections & Removals
Part 820 - Quality Systems Regulations
Part 821 - Medical Device Tracking Requirements
Quality System Inspection Technique (QSIT) - Guide to Inspections of Quality Systems August 1999
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