Accelerating Medical Device Innovation
Our vision
Have a great medical device idea, but need cost-effective design expertise to move it forward?
We specialise in turning early-stage concepts into production-ready designs, complete with CAD models, technical drawings, material specifications, and prototypes.
Whether you’re sketching on a napkin or refining a proof of concept, we’ll help you:
Develop precise CAD models & engineering drawings
Select components & materials
Coordinate rapid prototyping & testing
Liaise with manufacturers for a smooth handover
Optimise costs without sacrificing quality
Our services
Our services are designed to support every stage of your medical device journey, from early concept to market readiness. Whether you are entering the medical device sector for the first time or bringing years of industry experience, our expertise is structured to deliver meaningful value.
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We support the full product design journey, turning early concepts into well-engineered, functional devices.
Our capabilities span mechanical, electronic, and embedded system design, including electronics development, PCB design, and programming. By considering the complete system from the start, we ensure all elements work together seamlessly.
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Great design doesn’t stop at functionality, it must also be practical to produce. We apply Design for Manufacture principles throughout development to reduce complexity, control costs, and improve reliability.
This includes selecting suitable manufacturing processes, designing for efficient assembly, and minimising part counts where possible. The result is a product that not only works well, but can be produced consistently and economically at scale.
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Device development must align with regulatory expectations from day one. Our work is guided by in-depth knowledge of risk management (ISO 14971) and QMS standards (ISO 13485), ensuring regulatory thinking is built into the design process, not added as an afterthought. We design with global markets in mind, incorporating awareness of the regulatory frameworks in the EU, UK, and US. This approach helps streamline later verification and validation activities, saving time and reducing costs.
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Bringing a medical device to market requires more than good design, it requires a clear, well-timed development plan. We help you map the journey from idea to final product with practical, experience-based guidance at each stage.
We provide targeted advice on prototyping timelines, standards-based bench testing, clinical evaluation pathways, and the documentation needed to build a strong technical file.
Client testimonials
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[Med Design] approached the build with regulatory foresight, allowing us to align early design decisions with ISO 13485 and IEC 60601 requirements rather than retrofitting compliance later. I would not hesitate to recommend Med Design to founders developing early-stage medical devices, particularly those requiring optical, electronic, and firmware integration within a compliance-aware framework.
— Adail Islam (BioPhotonix Ltd)
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Med Design created the product design drawings for my device and I truly can’t recommend them highly enough. They were professional throughout the entire process, delivered everything I asked for, and consistently went above and beyond expectations. What really set them apart was their medical device expertise. Having someone with a strong med-tech background — not just product design experience — made a huge difference when developing the device plan. The whole experience felt seamless, collaborative and highly professional, and I’m incredibly pleased with the final outcome.
— Rachel MacKay (Tily Blooms Ltd)
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Med Design was outstanding in producing our bespoke phone cases, especially designed to fit clinical use. Throughout the process from design to production, Med Design had been friendly, patient and professional with us. We thoroughly enjoyed working with Med Design and look forward to any further collaborations.
— Alupha Chan (NHS Tayside)
Contact Us
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