SECTORS
MedTech
Medical Device Design & Development
Maximise device usability, minimise development risk
In MedTech, patient safety is the top priority. Taking a medical device from concept to manufacture in such a heavily regulated industry presents many challenges, and these are amplified if you lack sufficient domain knowledge, technical expertise or product development experience.
As an ISO 13485 accredited consultancy, we’ve been designing and developing medical devices for over two decades. This includes hospital and surgical equipment, point-of-care diagnostics and consumer healthcare products, including technology for drug delivery.
Healthcare organisations, medical professionals and researchers trust us to deliver products which are not only compliant, reliable and functional, but also integrate into existing clinical pathways.
Our engineers have deep expertise across the range of diagnostic and surgical technologies in every MedTech domain, including the emerging fields of FemTech and SportsTech.
A solution for every medical device challenge
Whether you are a start-up looking to bring a groundbreaking medical device to market, or an established company seeking to evolve your product offerings – or gain that crucial FDA compliance, CE marking, or UKCA marking – we can help.
Our engineers and designers can leverage their experience from a broad range of healthcare, consumer and industrial sectors to solve your medical device problem.
Healthcare companies call on our knowledge of MedTech, our expertise in designing medical devices, and our experience in providing an end-to-end development process.
Some of our clients work with us to improve their device usability, reduce production costs, and allow manufacture at scale. We’ve helped other companies unlock funding and take their innovation closer to commercialisation. Read our MedTech case studies to discover more.
Solving your problems with a multi-disciplinary approach
Our engineers have extensive experience across disciplines, developing customised solutions to take devices from concept to transfer for manufacture. We bring together expertise in industrial design, mechanical engineering, electronics, software development, and usability engineering.
This diverse skillset allows us to tackle complex challenges and deliver innovative solutions across a wide range of MedTech areas, including diagnostic devices, drug delivery, wearable technology, and digital health solutions.
Compliance for your medical device
As an ISO 13485 accredited medical device development consultancy, we have a deep understanding of the unique challenges and regulatory requirements of the MedTech industry, including FDA compliance, CE marking, and UKCA marking.
We can help you navigate this complex regulatory landscape with a meticulous approach to compliance.
Five successful outcomes for your device development
The benefits of an accredited medical device development consultancy with over two decades’ experience include:
Minimised
risk
thanks to proven risk management and quality frameworks, and comprehensive testing procedures to validate functionality, performance and reliability.
Compliance
experience
maximising the chances of your product obtaining regulatory approval.
Optimum user satisfaction
with products designed with usability engineering and human factors in mind from the outset.
Tough problems solved
because of our engineering expertise in software, electronics and mechanics.
Reduced manufacturing costs
enhanced production efficiency and improved scalability, thanks to efficient design iteration and our network of partners – from test houses and regulatory experts to suppliers and manufacturers.
Get in touch to discover how we can help you create safe, compliant and reliable medical devices to maximise commercial viability.
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