We are a specialist Human Factors Engineering organisation assisting medical device manufacturers and pharmaceutical companies in developing medical products.

THAY Medical focuses on the Human Factors (HF) aspects of medical devices as opposed to Clinical Research Organisations (CRO’s) who will focus on the clinical aspects of the medical devices. The human factors of a medical product can be described as the interaction between the user and the device. We believe it is vital to apply the best human factors and usability engineering practices into device developments and post-market surveillance. Good user interaction reduces the occurrence of clinical errors in real life.

We pride ourselves on complying with global regulations that are industry standard for medical devices – such as IEC 62366-1 and ISO 14971.

In addition, we also work to the US-based FDA requirements and European CE regulations. All services are performed to our own ISO 13485 certified quality management system. 

Our core services include usability engineering, human factors testing, medical device design, and much more which can be found on our “services” page. We operate to the highest industry standards globally, with focus on always exceeding regulations and customer expectations. We offer a solution tailored to your needs that always will be compliant, effective, and of great value.