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Learn how to get glowing remarks at YOUR next FDA/ISO audit.
Medical Device Manufacturers are faced with the constant challenge of meeting requirements for various FDA and ISO guidelines.
This case study highlights how a leading manufacturer of innovative technologies for the cardiac and vascular markets leveraged PLM software to create a controlled environment for managing product data and automating engineering change and training processes to successfully meet compliance and improve overall processes.
Be prepared for your next FDA and/or ISO audit! Read this case study.
Offered Free by: Omnify Software
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