Choosing the right technology is key for medical devices; it needs to perform both for functionality and safety. Whether you are looking at which MCU to choose, which sensors to select, or just to review the current state-of-art to include in your latest product, our expert engineers can provide key guidance on the assessment of technology from both a technical and compliance angle. 

We provide flexible programs of work to perform technology reviews, feasibility assessments, off-the-shelf product testing, viability reports and can generate proof of concepts. 

Are you looking to turn your idea into reality? We help companies of all sizes create market ready designs, ensuring that your product is fully tested, designed for manufacture and ready for launch. Using our c2 platform and over 40 years experience, our expert hardware and software engineers know the do’s and don’ts – making sure you get it right first time.

We provide software and electronics design, PCB layouts, software and analytics implementation, and product testing – everything you need to create a full prototype.

Medical products, especially electronics or software based products, must meet stringent regulatory requirements before release into the market. We are experts in designing products to match these regulatory frameworks, and testing products to prove it. This makes us the one stop shop for all your technical compliance needs.

We provide safety assessments, compliance reports to the harmonized standards such as 14971, 24971, 62304, 60601 and 62366. We undertake gap analysis assessments, so you know what you have to do standards. We can author and deliver technical document for you design history file generation.