Real world evidence solutions designed for MedTech.

IQVIA MedTech teams develop robust, flexible approaches for real world data as well as evidence collection, analysis, and application.
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The right data, the right expertise

IQVIA has an experienced MedTech team that understand clinical trial design strategy across the entire spectrum of medical devices, diagnostics, and combination products. Our solutions are focused on safety, effectiveness and value generation, and can support

  • Clinical trial design strategy
  • Long term surveillance and data collection
  • U.S., EU and Asia-Pacific regulatory insights and recommendations

Our strengths in real world data collection and analysis, coupled with domain-specific knowledge enable informed RWE generation from clinical trials to post-launch surveillance.

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