MedIntelliBase® Custom Literature Searches Fall Promotion Sign-up for Medical Device Companies

Are you in compliance with the new European Union Medical Device Directive requirements in effect as of October 15, 2013? Do you have the references you need for FDA submissions?

MedIntelliBase can help. We perform quick, thorough literature searches and reviews, providing comprehensive reports to support your medical devices.

Use our MIB Custom LitSearches™ to:

  • establish substantial equivalence to predicate devices
  • add new indications for use
  • support product improvements and new labeling claims
  • document adverse events
  • analyze specific patient populations

You benefit from:

  • Thorough, professional searches in compliance with FDA & EU MDD standards
  • Comprehensive view of the literature route
  • Verified findings with objective evaluations by medical literature experts
  • Fully documented and referenced point-in-time literature searches
  • Easy to access online summary reports & quickly searchable literature archives
  • Fully referenced & qualified results

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