SECTORS
LabTech & BioTech Equipment
Accelerating your product development
Developing laboratory testing equipment is a long, complicated process due to heavy legislation, strict market requirements and complex assay processes. The wrong product specifications early on can slow development and cause costly mistakes later.
Pharmaceutical companies, hospitals, and universities depend on our experience of developing LabTech equipment; R&D organisations also rely on us to help them develop BioTech platforms that further their research objectives.
Our team of experts start by developing early-stage laboratory test equipment and then move on to complete automation equipment. We’ve spent more than two decades creating marketable devices and development platforms, drawing on our knowledge and expertise in MedTech design and development as an ISO 13485 accredited consultancy.
This means we know how to formulate the right specifications for your product to guide compliance and seamless integration into clinical pathways. It also means we can help you to optimise and accelerate your product development, from concept through to transfer to manufacture.
A multi-disciplinary solution for your product challenges
Our engineers have vast expertise across five disciplines: industrial design, mechanical engineering, electronics engineering, software development, and usability engineering. They work on everything from sensor calibration rigs and in-vitro diagnostic (IVD) devices to microfluidics platforms.
This varied skillset allows us to tackle complex challenges and deliver innovative, customised solutions that take your LabTech and BioTech devices from concept to use in the lab.
Some clients come to us with a product that needs further development, for example to improve reliability or gain a new regulatory approval. Others need to identify user requirements for a new use case. To see how businesses work with us at the various stages of the development pathway, you can read more case studies here.
Whatever your product challenge, we can help you transform innovative processes, technologies and prototypes into certified devices and automated platforms.
LabTech and BioTech product compliance
Operating as an ISO 13485 accredited development consultancy, we have extensive understanding of the unique challenges and regulatory requirements of the LabTech and BioTech industries, including FDA compliance, CE marking, and UKCA.
We can help you navigate this complex regulatory landscape with a meticulous approach to compliance.
A user-focused approach for creating marketable devices
The discipline of usability engineering and human factors is fundamental to the success of every LabTech and BioTech product development pathway.
By tailoring different user studies to each stage of your project and incorporating other defined criteria – such as risk levels, use environment and workflow – we can craft the right questions and create the most suitable user interview sample.
With the results from this research, we can help you transform conceptual and lab-scale set-ups, processes and technologies into robust, marketable products.
Get in touch to discover how we can help you transform innovative concepts into certified, marketable devices and automated platforms.
What Our Clients Say…
”When we were creating the CN Bio PhysioMimix platform, eg technology provided us with access to the key skills and labour we needed. They worked well with our in-house team to transfer knowledge and provide ongoing support to sustain and extend the platform to meet the needs of our growing markets. We value our relationship with them.
Peter TempletonDirector - Product Development
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