IQVIA MedTech integrates the latest insights, expertise and technology to design and optimize protocols, recruit clinicians and patients, and drive transparent communication. Combined with expertise in budgets, sites, and study management, our approach ensures each solution is optimized for device research, so you stay on time and on budget.
Data-driven, highly integrated solutions create a truly connected offering, from pre-market development to post-market lifecycle support.
IQVIA MedTech can provide you with strategic insights into changing regulations, data, and technology requirements for medical device and diagnostics. We leverage our data-driven intelligence solutions and experts to design the right research for your product, information by our insights.
IQVIA MedTech's concept to market solutions and services help you orchestrate efficient research and development processes and decisions. Our comprehensive, integrated solutions and services create a connected offering from pre-market development to post-market life cycle support.
IQVIA MedTech maintains industry-leading medical device training and consulting programs. We hire and train technology, clinical, and regulatory experts that are fully dedicated to medical devices. In turn, they receive ongoing operational support from project managers and study monitors dedicated to medical device and diagnostics projects.
Tap into information from past trials, patient reported outcomes, and other sources to accelerate your research and build the necessary evidence for approval and access.
Quality, regulatory, safety and compliance solutions across the device lifecycle.