Home > Support > FDA Resource Center : Welcome
Content Authors: Please type in your comments below on what was changed or added.
Please keep existing comments that may be there for future recordkeeping, and include a date with your
comment.
Page Content
Please type in or update your page content below.
Wonderware FDA Resource Center
Wonderware is committed to meeting the needs of regulated industries that must comply with U.S. Food & Drug Administration (FDA) requirements, specifically 21 CFR Part 11.
To achieve this goal, we offer a full-fledged FDA resource center to show you how Wonderware products can be applied and deployed in implementing and maintaining 21 CFR Part 11-validated applications, third-party supporting tools and general FDA links to validation companies serving the market.
One of the key elements to working in the FDA-audited environment is that producers want to maximize their project lifecycles. If you can enhance and improve your applications while reducing the amount of new validation work, then you can save a significant amount of money.
The product improvements that Wonderware has been working on focus on lowering the implementation and maintenance costs of FDA-validated applications. Read our press release on Wonderware's Response To FDA 21 CFR Part 11.
