Europe, Middle East & Africa
Compliance orchestration, across the device lifecycle.
IQVIA MEDTECH解决方案是针对医疗设备和诊断行业的专门建造，并考虑到您独特的合规性需求。
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 qualityin your organization that extends quality and compliance maturity and reduces cost of quality (COQ)
- Adverse event reporting and post-market surveillancesolutions that make vigilance easy and sustainable
Our latest thinking about compliance for Medical Technologies
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