MedTech Resources & Insights
Our dedicated experts across IQVIA MedTech supports studies from trial design and delivery to commercial optimization.
Fact Sheets
MCRA Spine Solutions Overview
Download our brochure to see how MCRA’s team—including 25+ former FDA officials—supports spine devices. Learn about our global regulatory expertise, clinical trial management, market access, reimbursement, and quality assurance. With 1,000+ clinical site relationships, approvals in 30+ countries, and a 100% PMA approval rate, MCRA helps you bring spine technologies to market faster. Download now.
IQVIA MedTech Capabilities Overview
Navigate the complex MedTech R&D landscape with confidence. Download our PDF to explore IQVIA MedTech's comprehensive regulatory and full-service clinical trial outsourcing solutions. With 530+ MedTech trials conducted, we provide the expertise and support you need to manage evolving regulations and streamline your clinical development process. Download now.
MCRA is Now Part of IQVIA MedTech
By bringing together legacy expertise with total lifecycle solutions, MCRA and IQVIA MedTech help clients of every size and footprint move faster and smarter. Learn more.
Spine Success Story
Case Study: MCRA Assists Empirical Spine with Pre-Market Approval of Breakthrough Device, LimiFlex Dynamic Sagittal Tether
MCRA assisted Empirical Spine with all IDE regulatory activities, breakthrough device designation, CEC management, clinical trial support, modular PMA submission, and related FDA interactions, ultimately leading to premarket approval (PMA) of a novel motion-preserving spinal implant.
Our latest thought leadership
Global Market Entry: How to set up medical device clinical trials to meet global regulatory requirements
MedTech Trends Shaping 2026
Recent EUDAMED Requirements Put UDI Strategy Front and Center