Electronic Instructions for Use (eIFU)

Key Takeaways

Discover how Propel’s capabilities for eIFU enable you to:

• Manage eIFU within your Bill of Materials and New Product Development processes
• Eliminate errors due to content being spread across disparate systems
• Provide seamless access to your eIFU via a Community portal and Propel’s common platform

About This Resource

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.