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.
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In an age of disruption caused by rapid evolution of technology and volatility of supply, products must engage the market with a clear communication of their value.
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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.
By closing the quality loop, you can design, build, deliver, and service high-quality medical products for global markets faster and with more functionality.
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