Innovative solutions for MedTech orchestration from concept-to-market

The MedTech landscape is shifting, with challenges in the form of ever-changing regulatory requirements, market forces driving the need to introduce new medical device and diagnostic products, and innovative combination products, under difficult pricing and profitability conditions, and increasingly complex buying environments. This means that companies working in MedTech need specialist guidance and solutions as they move through and orchestrate the entire product lifecycle, from concept-to-market.

At IQVIA, our extensive understanding and our investment in MedTech solutions for medical device, in vitro diagnostics, and combination products companies allows us to operate within MedTech cost structures, and our deep domain expertise means that we will support you as you develop and execute clinical trials, enter into new markets, comply with regulatory processes, help you to find the resources and suppliers you need, orchestrating from concept to market.

IQVIA's MedTech solutions are tailored specifically to the medical devices and diagnostics industry:

  • End-to-end solutions provider that can break down silos across the product lifecycle
  • Geographic scale enabling support of an expanding number of markets
  • Trusted partner with deep regulatory and quality expertise
  • Access to cutting edge technology with advisory expertise and resourcing

 

MedTech Concept to Market Solutions

Our Solution

Clinical Solutions
Accelerate your clinical trials with our specialized full-service medical device and diagnostic CRO solutions, leveraging our comprehensive suite of data and laboratory solutions, supporting traditional, predictive and adaptive trials.
Commercial Solutions
Confirming product value and increasing return on investment based on product branding and positioning, launch support, commercial execution, and improved market measurement, with a technology-driven salesforce.
Quality, Regulatory, Safety and Compliance Solutions
Providing support during quality, regulatory, safety and compliance processes with validation and auditing services; and if things go wrong, providing back up through vigilance, safety and remediation services.
Real-World Evidence
Supporting faster, more precise decision-making and better product value and differentiation through real-world data, including outcomes research, health economics evaluation, market access strategy development and epidemiology and safety data generation.
Technology Solutions
Support all your MedTech activities with the latest in cutting-edge technology solutions. Ensure you have access to the right information, at the right time -- compliantly and efficiently.