Compliance orchestration, across the device lifecycle.

IQVIA MedTech solutions are purpose-built for the medical device and diagnostics industry, and designed with your unique compliance needs in mind.

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Delivering the rigor you need

As regulations governing medical devices and technology continue to evolve around the world, rigor and reproducibility in non-clinical, pre-clinical and clinical data - as well as the subsequent documentation - are essential.

From advice on strategies and portfolio analysis, to geographic-specific insights on regulatory authorities and revisions of post-market procedures, IQVIA's solutions span the entire product lifecycle. We can support

  • A robust, yet agile, quality management system (QMS) that enables you to respond to auditor or management requests swiftly and accurately with quality data and insights
  • A culture of quality in your organization that extends quality and compliance maturity and reduces cost of quality (COQ)
  • Adverse event reporting and post-market surveillance solutions that make vigilance easy and sustainable
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