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Wonderware FDA White Papers
Listed below are Wonderware white papers for regulated industries that must comply with FDA's 21 CFR Part 11 requirement.
Applying Wonderware in 21 CFR 11 Compliant Applications
This white paper provides a brief explanation of the Federal Drug Administration's "Title 21- Code of Federal Regulations-Part 11" and defines which Wonderware FactorySuite components are deployable under 21 CFR Part 11. Additionally, it defines Wonderware’s continued commitment to a software development strategy that reduces the cost of building and supporting 21 CFR Part 11 applications.
View the white paper (pdf)
Wonderware to Enhance Support for FDA Validated Applications
Throughout Wonderware's 16-year history, its R&D and product development strategies have been targeted at providing tools that facilitate automation application development and long-term maintainability at the lowest possible cost. This has been true for all industrial automation applications, but nowhere has it been more beneficial to users than in the production of food, drug and cosmetic products whose manufacturing processes are subject to regulation by the U.S. Food & Drug Administration (FDA).
View the white paper (pdf)
21 CFR Part 11 InTouch & IndustrialSQL Server Deployment Guide
This deployment guide offers information on InTouch and IndustrialSQL Server features relevant to the 21 CFR Part 11 requirements of the U.S. Food and Drug Adminstration ("FDA").
View the white paper (pdf)
