Whitepaper: Implementing 21 CFR Part 11 in epMotion® software
Posted: 30 November 2021 | Eppendorf | No comments yet
Electronic records and electronic signatures in the regulated environment of the pharmaceutical and medical device industries.
This whitepaper compares the legal requirements of 21 CFR Part 11 with the technical specifications of the hardware and software product epMotion® in combination with the epBlue GxP software.
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Biopharmaceuticals, Good Manufacturing Practice (GMP), Lab Automation, Manufacturing, Medical Devices