Discover how Propel’s capabilities for eIFU enable you to:
Electronic Instructions for Use allows medical device manufacturers to remain compliant with the EU Medical Device Regulation by automatically publishing and managing medical device instructions on publicly-available websites. Learn more about Propel’s capabilities for eIFU.
The lack of an efficient digital product thread significantly hinders company growth. Learn how to exceed revenue goals and customer expectations by better connecting your team and processes through a central technology solution.
Learn about what this integration does for you, and the associated capabilities and benefits.
Implement company-wide quality management processes that are tailored to your specific needs.
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