End-to-End Medical Device Consulting
Services designed to build on one another seamlessly. Our process is built on a foundation of speed, transparency, and trust, ensuring your project momentum never stalls.
Redefining Medical Device Consulting with Integrated Expertise
Veranex provides comprehensive medical device consulting that unites strategy, development, and execution under one roof. Our clients face a difficult market with pressures to innovate while reducing R&D budgets and navigating complex regulations. Traditional consulting models, which rely on a fragmented network of vendors for design, testing, and regulatory affairs, create friction and risk at every handoff. We eliminate those silos.
35
+
Years of product development experience
800
+
Cross Functional Disciplines
1500
+
FDA submissions and Amendments
2500
+
Preclinical and Clinical Projects Completed
Integrated Medical Device Consulting: From Concept to Commercialization
The only partner that combines world-class product design and engineering with an international medical CRO and deep regulatory, quality, and market access expertise. This unified approach delivers unparalleled value and impact for our clients to effectively navigate all phases of the medical device lifecycle.
Early-Stage Strategy & Opportunity Assessment
Have you identified all pathways to growth?
Successful medical device consulting begins with a robust commercial strategy. We help innovators assess market opportunities, which includes sizing the market, forecasting adoption, and analyzing the competitive landscape to define a clear value proposition. For clients seeking inorganic growth, our teams are well-positioned to bring external reimbursement and development expertise to support M&A and due diligence efforts.
Integrated Medical Device Design
Are your design inputs aligned with your stakeholder needs and regulatory requirements?
We engage our development teams with regulatory and quality experts from the very beginning. This critical, early integration ensures your product's design inputs are directly informed by regulatory requirements and clinical needs, creating a streamlined development strategy. This proactive approach to medical device design mitigates risk and ensures the final product is primed for both user adoption and successful submission.
Clinical & Regulatory Execution with a Medical CRO
Is your evidence strategy built for both regulators and the market?
As a strong, international medical CRO, we provide comprehensive services to prove your device is safe and effective. We support all phases of clinical investigation, from First-in-Human and feasibility studies to pivotal trials designed to support market submissions to the FDA and EU regulatory bodies. We finalize development by supporting the creation of all submission deliverables and ensuring a seamless transfer to manufacturing, making us the one-stop shop for market readiness.
What Clients Say
"Since we launched our redesigned TAVR delivery system, which was led by Veranex’s design and engineering teams, we’ve seen that the performance of the valve itself has improved."
By R&D Director, Large Medtech
What Clients Say
"Together, we've successfully transformed two groundbreaking concepts from napkin sketches into viable products"
CEO, Medical Device Company
What Clients Say
"This is terrific. First of all, I am so impressed with how quickly you turned this around. This has been a big question that our team has been grappling with for a while so this is amazing to see this come together so quickly and give us a very thorough and thoughtful response.”
By Jennifer Fried, CEO at Flow Medical
The Innovation Contract Research Organization to Reach Your Medical Device Goals
Integrated cross functional teams that aid in streamlining development and accelerating success.
Streamline Your Project with Integrated Medical Device Consulting
Our experts unite medical device design and CRO services to de-risk your project and ensure a seamless submission and successful launch.
