Movement is a Usability Engineering and Biomedical Design resource headquartered in Dublin, Ireland with a subsidiary in Cleveland, Ohio, USA. Usability and Human Factors Engineering are of paramount importance in the medical device industry due to the statutory regulatory requirements from standards such as ISO/IEC 62366:2007, ISO/IEC 14971:2007 and the ANSI/AAMI HE75: 2009. Movement manage and deliver the Usability Engineering File (UEF) for inclusion into QC documentation relating to the HFE Plan & Product Realization for ISO 13485:2003. For Class II or Class III special controls the Title 21 CFR requirements will be adhered to. Movement also manages and conducts comprehensive Formative Prototype Verification Tests and Summative Human Factors Validation Tests.
“Movement deliver the Human Factor through Biomedical Usability Design”
In the past 5 years Movement has collaborated across the globe on over 100 different med tech devices. No other medical design service company can boast such a comprehensive CV. Above you can see four general areas which list some of the vast array of biomedical projects Movement have been involved in. Movement’s dedicated experience and skillset is unique and unparalleled in the design service industry.
The metrics for measuring our success are the sales figures for our client companies’ related product lines. Collectively the products we have collaborated on currently gross an annual sales figure in excess of €500m, and this is growing each year.
Our business is built on delivering world class results to our clients in the med tech and pharma sector in a highly confidential manner. We are NOT a ‘Product Design’ consultancy, we ARE a Biomedical Usability Design consultancy. We are different, come and meet us to discuss your project and understand how and why.