Brochure
IQVIA MedTech Consulting Capabilities
Your trusted medical device partner with deep therapeutic expertise, unmatched data assets, and healthcare-grade technology
Aug 26, 2025
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The MedTech industry is evolving faster than ever. Market access pathways, regulatory expectations, and global trade challenges can quickly complicate your growth journey.

That’s where IQVIA MedTech Consulting comes in. With deep therapeutic expertise, unmatched data assets, and healthcare-grade technology, we help innovators cut through complexity and deliver meaningful solutions to patients worldwide.

We bring together 2,500+ dedicated MedTech domain experts, and access to the world’s most comprehensive healthcare data ecosystem. Our proven methodology, powered by real-world insights and an extensive network of industry experts, ensures your decisions are founded on robust evidence and tailored for impact.

Trusted by 1,600+ MedTech companies in 80+ countries, our consulting team is built around your purpose—so innovation thrives where it matters most.

Ready to take the next step? Download our brochure and click the CONTACT US button to start a conversation about how we can partner with you to accelerate your MedTech journey.

Built to help you thrive in MedTech.

Clinical strategy and evidence generation

Strengthen clinical strategy with expertise in trial design, evidence generation, and post-market surveillance—powered by real-world data and advanced analytics.

End-to-end market access expertise

From coding strategy to payer engagement and reimbursement optimization, we guide MedTech innovators through every phase of product access—globally and locally.

Track evolving regulations with confidence

Stay ahead of dynamic compliance requirements with real-time insights into policy, pricing reform, and procedural updates—including China’s VBP, EU MDR, and FDA pathways.

Navigate global trade challenges

We help you assess the impact of tariffs and other trade barriers, enabling informed decision-making for supply chain planning, localization, and pricing strategy.

Elevate quality & safety systems

Our consulting integrates our technology, automation, digital quality frameworks, and real-world evidence to support robust, compliant quality and safety management programs.

Data-driven commercial strategy

Leverage IQVIA’s unmatched data ecosystem—over 1.7B medical claims, 800K+ data feeds, and global research infrastructure—to shape winning go-to-market plans.
2,500+

MedTech domain experts matched to device category for tailored support

15+

therapeutic areas have an IQVIA MedTech clinical and commercial team structured around them including orthopedics, cardiovascular, neurology, diagnostics and digital health

600+

device studies have been conducted by IQVIA MedTech across 300+ sites with 200,000+ patients enrolled

MedTech is a completely unique space within the life science industry. Our experts have decades of experience with MedTech Market Access, Primary Intelligence, Strategy and Data – we translate our breadth of resources into specific solutions for medical device companies.
We work side by side with MedTech innovators, combining expertise and data-driven insights to turn complexity into confident, strategic decisions.
With over five decades of IVD expertise, IQVIA MedTech combines a time-tested approach and unmatched access to industry experts to create the most robust market models—providing the insights clients need to drive decisions and deliver on their objectives.
At IQVIA MedTech we bring hands-on experience, strong data, and a clear understanding of how the MedTech market works. Our focus is on solving real problems—whether it's opportunity assessment, navigating regulatory pathways, or driving market access.
Michelle Edwards
VP, Consulting and RWE, IQVIA MedTech
ZhenNie
Head of Med Devices, Global Consulting, IQVIA MedTech
Vladimir Nozinic
Associate Director, Diagnostics & Diabetes Consulting, IQVIA MedTech
Megha Maheshwari
Engagement Manager, Consulting, IQVIA MedTech
Ready to take the next step?
Purpose-built for MedTech, we are fully aligned with your mission to improve lives. Start a conversation about how we can partner with you to accelerate your MedTech journey
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IQVIA MedTech combines 50+ years of MedTech expertise with the industry’s most comprehensive healthcare data ecosystem and 2,500+ domain experts worldwide. Our unique blend of data-driven insights, regulatory knowledge, and commercial strategy helps MedTech innovators cut through complexity and accelerate growth.
IQVIA MedTech’s consulting integrates with purpose-built Compliance Solutions to help MedTech companies align strategy with execution. From enterprise QMS development to regulatory intelligence and adverse event reporting, we ensure compliance strategies are embedded into broader business planning—reducing risk while supporting long-term growth.
Our consulting teams help design and optimize clinical strategies that accelerate speed-to-market and strengthen evidence generation. Leveraging IQVIA MedTech’s global data, real-world evidence expertise, and advanced technology, we guide MedTech innovators through PMA clinical performance studies, post-approval surveillance, and evidence planning—ensuring robust support from early development through commercialization.
Evidence is central to IQVIA MedTech consulting work. We help clients build value messaging, design evidence plans, and leverage real-world data to demonstrate safety, performance, and cost-effectiveness. This evidence not only supports regulatory submissions but also strengthens reimbursement, payer engagement, and commercial adoption.

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