The spring of 1997 was a significant time for theFood and Drug Administration (FDA). An overhaul of the Agency’s Good Manufacturing Processes (GMP) brought changes that had not been seen for a quarter ...
The FDA established the Electronic Records and Electronic Signatures Rule (21 CFR Part 11) in order to outline the necessities for electronic form records and the accepted electronic signatures ...
REDWOOD CITY, Calif.--(BUSINESS WIRE)-- Box, Inc. (NYSE:BOX), the leading Content Cloud, today announced that its native e-signature product, Box Sign, has achieved support for compliance with FDA 21 ...
The regulations for food and drugs in the United States, described in Title 21 of the Code of Federal Regulations (CFR), are critical in ensuring safe and ethical drug administration. Whether you are ...
Agilent Technologies Inc (NYSE: A) today announced the release of a new 21 CFR Part 11 compliance software for the Agilent xCELLigence Real-Time Cell Analysis (RTCA) eSight system. The software ...
Web-enabled and Ethernet-ready, this liquid filler makes it easier for drug makers to generate FDA-recommended electronic record-keeping. The Micrologix controller (top) on board the liquid filler ...
You’re under pressure to innovate quickly and improve patient outcomes. Don’t let paper-based processes, legacy GxP technology, and app sprawl slow you down. Speed up R&D, maintain GxP compliance, and ...
DeNovix Inc. announces the launch of EasyApps Secure, a 21 CFR Part 11 Compliance Ready software option for CellDrop Automated Cell Counters. The new suite of controls for EasyApps software enables ...
SANTA CLARA, Calif.--(BUSINESS WIRE)-- Agilent Technologies Inc (A) (NYSE: A) today announced the release of a new 21 CFR Part 11 compliance software for the Agilent xCELLigence Real-Time Cell ...
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