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Interpretation of 21 CFR Part 11
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7
Interpretation of 21 CFR Part 11
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59.95
Creation of Installation Qualification Protocols
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49.95
Third Party Change Control Oversight
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39.95
Gowning Requirements
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49.95
Batch Record Review
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39.95
Medical Device Reporting
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39.95
Corporate QA Audits
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Master Batch Records and Batch Record Issuance
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