We design products and devices with usability at the heart so that they are safer, easier to use and enjoyed by their users; from patients, to clinicians, to carers.
To meet the requirements of a highly regulated industry, we consider human factors from the offset of each project. Human Factors Engineering (HFE) focuses on the interactions between people and devices and ultimately aims to enhance safety by minimising use-related hazards.
Our human factors service helps you understand your end-users’ capabilities, needs and desires, to improve overall user experience thus also adding commercial value to your product or device.
We are advocates for user centred design. Whilst we have a network of specialists, healthcare professionals, and users in a number of sectors, we also harness your network throughout the design and development process.
Beyond grave scenarios, there are many wider benefits to incorporating HFE into device design & development including;
In addition to our multi-disciplinary in-house team, we utilise our network of industry experts to ensure impartiality and provide services to support you with;
HD provided the design & development of an innovative urinary drainage device with a number of novel features drawn from user needs....
In light of World Diabetes Day, we spoke to Chris Harrison, who has been living with Type One Diabetes for over 40 years to learn about his experiences of Diabetes Care....
Human Factors Engineering (HFE), focuses on the interactions between people and devices to minimise use-related hazards and enhance patient safety. Senior Design Engineer, John, and Human Centred Desi...
Next in our user series, we chat to Tayla Collinson, a 27-year-old who manages a number of chronic conditions and is currently living with a suprapubic catheter. ...
Despite regularly working on a variety of product and medical device projects, there are always improvements to be made and taking the time to really understand user needs is often a crucial piece to ...
User experience and human centred considerations can, and should, be applied to the design and features of all medical devices – it’s just that they sometimes aren’t. While its paramount that a...
It is no secret that risk management isn’t the most exciting subject to speak about, but it is an essential part of all design and engineering, particularly for medical devices. Whether you’re new...
Although they differ in finer detail, both the European and U.S. regulatory laws discuss Design Controls. Failure to comply with these laws can result in a series of penalties including your device be...