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Supporting the full MedTech clinical development cycle
Clinical
Technology
Regulatory
Add-On Services
Real World Evidence
Feasibility and Site Selection Clinical Project Management Monitoring and Site Management Data Management & Programming Biostatistics Safety Management DSMB & CEC
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IQVIA Research Management Platform EDC PROM CEC Module Image tracking
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Strategic consultancy Device and IVD Classification EU MDR and IVDR readiness FDA, Notified Body and agency filings and meetings Study design and documentation
Post-Market Safety Device Registries In Vitro Diagnostics Non Interventional Studies Digital Health Outcomes Studies
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IVD development process services Laboratory Developed Tests (LDT) Predicate device access Central lab in close vicinity Biorepository services Genomic Lab
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Strategy Consulting
Contract Performance Solutions
Patient Services
Analytics Solutions
Patient Access & Affordability Solutions
