"Through human research, intelligent design thinking and exemplary realisation, movement intend to create human focused solutions which exceed our client’s and their customer’s expectations."
We are a Human Centred Design resource based in Dublin, Ireland. Human Factors Engineering (aka Ergonomics) is of paramount importance in the medical device industry. This is due to the increasing regulatory pressures from standards such as;
ISO/IEC 62366:2007 Medical Devices - Application of Usability Engineering to Medical Devices
ANSI/AAMI HE75: 2009 Human Factors Engineering – Design of Medical Devices
CLIA Certificate Of Waiver (Clinical Laboratory Improvement Amendments)
Movement support our outputs with documentation which adheres to the above and other related standards. This is used by our clients for inclusion into their QC documentation relating to their HFE Plan & Product Realisation for ISO 13485:2003. For Class II or Class III special controls the Title 21 CFR requirements for the device solution will also be adhered to.