FDA 21 CFR Part 11

Electronic Records and Signatures for CGMP Compliance

If electronic records are used for submission to FDA (as opposed to paper records of data) they must be secured through multilevel password and duplicate record maintenance protection schemes. Must not be alterable and must have some assurance that access is limited and controlled.

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Ultra Vision Online Ultra Vision Online
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HIAC PharmSpec 2
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  • USP<788>, EP, JP, or KP compendial tests
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