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 ...
SAN FRANCISCO--(BUSINESS WIRE)--Morf Media Inc., shaping the future of enterprise talent development and compliance training, today announced an interactive FDA compliance training course, 21 CFR 11 - ...
Dublin, Jan. 07, 2026 (GLOBE NEWSWIRE) -- The "FDA's 21 CFR Part 11 Add-on Inspections (Jan 12, 2026)" training has been added to ResearchAndMarkets.com's offering. The verification and validation of ...
Dublin, Dec. 04, 2024 (GLOBE NEWSWIRE) -- The "21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries" webinar has been added to ResearchAndMarkets.com's ...
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 ...
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 ...
TORONTO, May 7 - Axela Inc., is pleased to announce the release of a software package for the dotLab(R) System that provides technical controls to support compliance with 21 CFR Part 11 regulations.
The purpose of this paper is to present an approach to assist the user in meeting 21 CFR Part 11 compliance with Analyst® LC/MS Software version 1.2 and above, including Analyst Software 1.4.1, when ...
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