MedTech
Medical Technology Device Development
Tailored consulting for high-impact medical technology device development
Developing innovative, high-impact medical technology devices requires prioritizing speed without sacrificing quality, compliance, or return on investment. CDP provides tailored, targeted support for the entire lifecycle of developing a new product, from early feasibility all the way to verification, validation, and regulatory submission.
Whether you need support throughout the entire development process or in a specific stage, CDP acts as an extension of your team and works within your parameters. Our cross-functional teams have expertise in design, engineering, testing, and regulatory matters, enabling us to deliver usable, compliant, and manufacturable devices.
Accurately Estimating Blood Loss. Navigating Design Challenges and Pioneering Future Solutions
In this article, we will explore the challenges of estimating blood loss (EBL), evaluate the advantages and disadvantages of various novel solutions, and discuss the key factors necessary for achieving more accurate, timely, and insightful monitoring.
Capabilities
Positioned for Innovation
Located at the heart of innovation in Cambridge, UK, and Raleigh, North Carolina, our bases are strategically positioned to tap into the world’s leading research and development communities.
ISO-Certified Management System
To support our product development and prototype manufacturing services, CDP’s Quality Management System is certified to ISO 13485:2016 by Intertek Medical Notified Body and ISO 9001:2015 by Intertek Certification Ltd. We are also certified to ISO 27001:2022 by Intertek Certification Ltd to support the maintenance of the confidentiality, availability and integrity of our clients data.
Client-Centric Intellectual Property Approach
Our clients fully own all intellectual property we help create. We equip them with the tools and knowledge to enable lasting independence.
Meet The Team
Corey Smigelski
Wajeeh Chaudhry
Tom Brittain
Jack Hornsby
James Boonzaier
Featured Insights
How fast can you bring new Surgical Robotics tech to market? Know the 3Cs to rapid development.
CDP advances surgical robotic technology
Single-Use Endoscopes: A Greener Solution?
FAQs
Explore our FAQs to find out more about how our expert team can help turn Medtech challenges into medical devices that are safe, reliable, and ready for clinical use.
What does “medical device development consulting” include?
It typically includes user research, concept development, engineering, prototyping, human factors, design controls, risk management, verification and validation, and transfer to manufacture.
When should we bring in an external development partner?
When you need additional capacity, specialized expertise, faster iteration, independent human factors rigor, or help accelerating V&V and regulatory readiness
Can you support regulatory submissions?
Yes. We support design controls, risk management, usability engineering documentation, and V&V evidence packages that teams use within their submission workflows.
Do you work with both startups and large MedTech companies?
Yes. We flex from focused feasibility sprints to multi-year programs that scale with your pipeline and internal teams.
What Medtech segments do you specialize in?
Surgical robotics and MIS, cardiovascular and structural heart, renal and blood filtration, wound/ostomy/continence care, and ICU/acute care systems.