Are you in compliance with the new European Union Medical Device Directive requirements in effect as of March 21, 2010? MedIntelliBase can help. We perform quick, thorough literature reviews and provide comprehensive reports to support your medical devices.

  • Obtain a thorough, professional review in compliance with the EU MDD
  • Comprehensive view of the literature route
  • Verified findings with objective evaluations by medical literature and regulatory experts
  • Fully documented and referenced point-in-time literature review
  • Establish substantial equivalence to predicate devices
  • Fully referenced & qualified analysis

The details

  • Obtain a no-obligation, free custom quotation for LitReview service by completing this form

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