US FDA CFR Pt 11RSS

Designed with the healthcare industry in mind, the US FDA 21 CFR Part 11 regulations outline criteria for accepting electronic records and electronic signatures as equivalent to paper-based records and handwritten signatures. FDA 21 CFR Part 11 also provides guidelines for documenting and validating authorized change processes to systems and software involved in the creation of electronic documents.
Tripwire Enterprise

Tripwire Enterprise is the configuration control solution that combines best-of-breed file integrity monitoring with comprehensive compliance policy management to protect, detect and correct IT systems throughout the modern enterprise. As a part of the Tr ...

VendorTripwire, Inc.
Pricing ModelCommercial
Modified

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