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.
With smart factories on the rise, it's more important than ever to stay up to speed with the changing manufacturing jargon. Here's a handy list to keep around wherever you go.
Implement company-wide quality management processes that are tailored to your specific needs.
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