Are you in compliance with the growing demands of European Union drug and device directives? 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 biologics, drugs and their delivery systems.

Use our MIB Custom LitSearches™ to:

  • support New Drug Application (NDA) filing
  • add new indications for use
  • support combination drug and new labeling claims
  • document safety issues, adverse events and hazards
  • analyze specific patient populations
  • establish substantial equivalence to predicate devices integral to drug delivery systems

You benefit from:

  • Thorough, professional searches in compliance with EU & FDA regulations
  • 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
  • Option for periodic updates to build your online literature archives

Special Offer

Acquire an introductory MedIntelliBase LitSearch of up to 100 targeted abstracts for only $1,995 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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