Neuromodulation
Neuromodulation Device Design and Development
An ISO 13485-certified partner for neuromodulation and neurotech devices, from initial concept through to production.
Cambridge Design Partnership (CDP) is a medical device design and development consultancy for neuromodulation and neurotech companies. We develop implantable neurostimulation systems, implant delivery systems and external devices, for therapies such as spinal cord stimulation. Whether we start with your initial concept or join at a later stage of development, we work flexibly with your team to make sure your innovation is feasible, usable, commercially viable, compliant, manufacturable and wanted by users.
Our collaborative expert team can address a wide variety of your needs such as to:
- Gain further insights on user and stakeholder needs to refine your innovation
- Develop and test technical solutions for implantable devices, delivery systems, or external devices
- Design engaging, usable solutions for patients and clinicians
- Conduct formative and summative human factors (usability) studies
- Transform proof-of-concept prototypes into production solutions
- Build digital and data science strategies
Navigating Neuromodulation Innovation Trends
Neuromodulation is changing fast. Companies are pursuing less invasive implant procedures, longer-lasting power through efficient through-body charging, MRI conditionality, closed-loop therapies driven by data analytics, new stimulation waveforms, and companion apps that help patients stay engaged with their therapy. Each trend brings technical, usability, regulatory and commercial challenges.
CDP applies innovation methods built for these challenges and tailors the approach to your therapy and commercial goals.
Neurotech Trends
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 Development and Manufacturing
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.