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      Courses #21 CFR


      3 Hours Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries

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      The US FDA QMSR Transition - 21 CFR 820 And ISO 13485

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      21 CFR PART 11 COMPLIANCE FOR ELECTRONIC RECORDS AND SIGNATURES

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      Effective Design Control (21 CFR Part 820.30)

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