All our medical device innovations, our inventions and ideas for the future of healthcare come from the research that we carry out on our users needs. Every product extension and next generation device is designed to improve patient comfort, user requirements, safety and ease-of-use.
By integrating human factors into all our product design, the entire journey is consumer-focused and has the supporting in-use data, in addition to clinical data required by 3rd parties such as FDA, MHRA and SGS.
Our human factors engineering and usability engineering confirm that our products are designed with patients and healthcare professionals in mind, making it as easy and as safe as possible for the end-user to adhere to a treatment regime. This is achieved by establishing user requirements early in concept phase using Human Factors best practice, and insights from on market surveillance, formative testing and targeted research. This process is heavily supported by user evaluations on all parts of the device interface to ensure that potential for error and difficulties can be identified and controlled to minimise use risk.
