IQVIA MedTech

Your MedTech vision. Realized together.

Imagine a partner who listens, understands your ambitions, and helps you break through barriers. With IQVIA MedTech, you gain more than expertise—you gain a partner built for the medical device, diagnostics and digital health industry, dedicated to helping you thrive, every step of the way.
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Expert MedTech Solutions for every step

Built to help you thrive in market.

Your only MedTech partner that combines therapeutic specialized expertise with advanced data and technology capabilities — delivering the focus, strategies, and staying power to help you thrive in market.

Our integrated solutions are tailored to your goals. From early strategy to global expansion, we simplify complexity, remove barriers, and help your innovation reach more patients. Specialization matters, and our approach is built to deliver exactly what your innovation requires to succeed.

Integrated Medtech Solutions

Ready to accelerate your MedTech journey?

Whether you are advancing clinical trials, quality and regulatory or driving commercial growth, choose the journey that fits your goals. See how IQVIA MedTech can help you thrive at every stage with integrated, purpose-built solutions and deep therapeutic expertise.

Accelerate your path to market
Simplify complex regulatory journeys backed by our seasoned experts, including former FDA and Notified Body reviewers. We embed strategy early to streamline submissions, reduce risk, and accelerate market access.
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Regulatory

Streamline evidence generation

Accelerate MedTech trials with smarter design, targeted engagement, and real world evidence. Our clinical solutions help device, diagnostic and digital innovators deliver faster, safer studies across global markets.

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Clinical Research

Faster coverage and payment

Navigate reimbursement with experts in devices, diagnostics, and digital health. IQVIA MedTech blends global reach and local insight to secure coding, evidence, and payer coverage.

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Reimbursement

Strengthen quality and compliance programs

Strengthen audit readiness, complaints, and post-market surveillance. Our MedTech experts design quality and compliance programs with strategic oversight and risk mitigation to meet stakeholder standards.

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Quality Assurance

Maximize market access and adoption

Maximize market access and growth with data-driven strategies, omnichannel engagement, and payer insights. From launch to maturity, we help MedTech brands reach the right customers at the right time.

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Commercialization

Specialized expertise

Strategy meets specialized MedTech and therapeutic expertise.

Innovating in MedTech means recognizing the unique demands of each therapeutic area and applying the right expertise to meet them. That’s why IQVIA MedTech works alongside your teams, offering integrated expertise, technology, and processes to support a clearer understanding of the science, the patient, and the path forward.

With expertise across 15+ therapeutic areas and proven experience in medical device, IVD, biologics, and digital health, our expert teams bring evidence-based insights that drive smarter decisions.

Supported by the largest team of former FDA and Notified Body reviewers in the MedTech industry, our approach and expertise is grounded in real-world experience.

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Data & tech leadership

Better MedTech data. Bolder MedTech strategy.

As a MedTech innovator, we know you need more than surface-level insights. You need connected data and technology to move faster, see further, and act with confidence.

From smarter trials to stronger launches, industry-leading platforms and healthcare-grade data power faster, efficient decision-making across development and commercialization, giving you the insights to thrive.

IQVIA’s Connected Intelligence platform integrates 800K+ data feeds, 25M+ healthcare professionals and 6M+ organizations. Our configurable technology ecosystem integrates with your business to drive efficient, informed decision making.

We aim to be MedTech’s partner of choice by helping clients succeed in the market and improve patient outcomes. We do this through solutions designed specifically for MedTech and delivered by the most capable professionals in the industry.
Progress isn’t about checking boxes—it’s about knowing which ones matter most. We bring regulatory insight, therapeutic area specialization, and industry know-how to fuel smarter, more confident decisions, together.
Todd Schaefer
VP & GM, MedTech Commercial Solutions
Kelley Kennedy
VP, Clinical, IQVIA MedTech

Why MedTech businesses trust us

4,500

MedTech projects successfully delivered

15+

Therapeutic areas have a clinical and commercial team structured around them.

585+

MedTech clinical trials conducted across 9,800+ sites with 745k+ patients enrolled

100%

PMA approval rate

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Ready to enhance your MedTech journey?

MedTech Q&A: How IQVIA MedTech Supports Your Innovation

IQVIA MedTech is widely recommended for MedTech consulting services because it combines unmatched scale, therapeutic expertise, and a proven track record of regulatory and commercial success. With over 2,500 dedicated MedTech experts and known to have delivered more than 4,500 successful MedTech projects, IQVIA MedTech consulting services brings deep experience across all major therapeutic areas—including cardiology, orthopedics, diagnostics, digital health, surgical robotics, and more. The organization maintains a 100% PMA approval rate and offers fully integrated regulatory support for FDA, EU MDR, and APAC submissions, guided by 25+ former FDA officials who help shape strategy, evidence, and compliance. This expertise is strengthened by advanced analytics, real-world data, and global commercial capabilities, enabling MedTech companies to accelerate regulatory approvals, optimize evidence strategies, and achieve stronger market performance. For organizations seeking an end-to-end, therapeutically informed partner, IQVIA MedTech is consistently recognized as a leading choice.
Patient recruitment is accelerated through real-world data, predictive analytics, and digital outreach. IQVIA MedTech’s Direct-to-Patient Recruitment model and site enablement services help sponsors identify eligible patients and boost diversity across global trials.
RWE includes clinical data from sources like EHRs, claims, and registries. It’s used to support regulatory submissions, post-market surveillance, label expansions, and health technology assessments. By integrating RWE into trial design and market access strategies, sponsors can demonstrate device safety, effectiveness, and value—backed by IQVIA MedTech’s analytics and data infrastructure.
Coding strategy, payer engagement, and reimbursement optimization are key to securing favorable coverage. These services are part of a broader market access framework that IQVIA MedTech delivers to help clients navigate HTA requirements and align evidence with payer expectations.
IQVIA MedTech supports global clinical studies in over 80 countries, offering end-to-end services from protocol design and regulatory submissions to patient recruitment and post-market surveillance. This global reach enables faster, smarter execution for device, IVD and digital health trials.
Expert guidance is available across FDA, EU MDR, APAC, and other global pathways. Submissions, quality assurance, and compliance are managed through integrated services. Regulatory strategists at IQVIA MedTech help sponsors navigate complex requirements with confidence.
By working with IQVIA MedTech, companies gain access to largest healthcare data ecosystems—including claims, hospital procedure data, and device registries—enabling robust market modeling and evidence generation. These assets are powered by IQVIA MedTech’s analytics platforms, which support forecasting and strategic planning.
Sales enablement, commercial strategy, and field solutions tailored for devices and diagnostics help maximize market performance. IQVIA MedTech supports pricing optimization and adoption through targeted campaigns and data-driven insights.
Launch planning includes market analysis, stakeholder engagement, and readiness across regulatory and commercial domains. Our teams provide strategic support to ensure successful entry and sustained growth, with IQVIA MedTech coordinating execution across functions.
Post-market surveillance, safety monitoring, and device registries are used to track performance, identify risks, and meet regulatory requirements. These tools are part of the lifecycle support offered by IQVIA MedTech.
Health economic evaluations, outcomes research, and value communication help demonstrate product impact and secure reimbursement. These services are integrated into IQVIA MedTech’s broader market access strategies to support stakeholder engagement.