Medical devices utilise Omnify PLM technology
An
Omnify Software product story
Edited by the Engineeringtalk editorial team
Jan 15, 2009
Omnify Software has announced that they have seen an increase in the number of medical device manufacturers implementing its PLM technology.
PLM is able to support controlled design processes and manage data for FDA (Food and Drug Administration) compliance.
Many of Omnify's medical device customers are leveraging Omnify Empower PLM to meet requirements set by the FDA regulation Part 11 of Title 21 of the Code of Federal Regulations (21 CFR Part 11), and the FDA 21 CFR Part 820 Quality System regulation.
These customers have also completed the Software Validation process mandated by the FDA for software used to design, develop, or manufacture medical devices.
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