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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.

Medical Device Case Study: Ensure Successful FDA/ISO Audits with PLM Software, Omnify Software, Omnify Software Complimentary Case Study, Medical Device Manufacturers, innovative technologies, cardiac and vascular markets
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Medical Device Case Study: Ensure Successful FDA/ISO Audits with PLM Software
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