The IQVIA MedTech Consulting brochure presents services that help medical device and IVD companies navigate access, regulation, and growth. Expertise includes clinical strategy, trial design, real-world evidence, and post-market surveillance. Market access support spans coding, reimbursement, and payer engagement. The team also tracks regulations like EU MDR, FDA pathways, and China’s VBP, while guiding supply chain, pricing, and localization. With 2,500+ domain experts, 600+ device studies, and presence in 80+ countries, IQVIA delivers tailored support across 15+ therapeutic areas, including orthopedics, cardiovascular, and digital health.

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