Are you in compliance with the new European Union Medical Device Directive requirements in effect as of March 21, 2010? 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

Special Offer

Acquire an introductory MedIntelliBase LitSearch of up to 50 targeted abstracts for only $995 AND receive a 25% discount off our list price for any other MedIntelliBase LitSearch service.

Learn more about MedIntelliBase Custom LitReview services. Please contact me.

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