Specifying, buying and assessing healthcare products presents one of the best opportunities to control risks to patients (and staff) safety.

2019 to 2020 saw 54,812 patient safety incidents identified as being related to medical devices and equipment.

This figure is likely to be more.

In 2017, for example, 260,000 diabetics experienced a hospital based medication error in the UK sparking a national investigation by the Healthcare Safety Investigation Branch (HSIB) into the use of insulin pen devices.

It’s widely recognised that using Human Factors increases the likelihood that a medical device or equipment will be safe, easy to use, effective, efficient and satisfying when people use it.

Regulations and Standards mandate that designers must use Human Factors during the design of medical devices. But this is not enough. Use-errors still occur, when designs, for example, confuse the user or are inconsistent, fail to meet users’ needs and expectations, do not do what is needed or are used in an inappropriate situation.

We produced a document in 2020 Selecting safe & easy to use products – using Human Factors Specification & Checklists which we have now made editable for you to use.