BEC and its associates provide engineering services to start-up entities who seek to develop, validate, test and obtain regulatory clearance/approval for commercialization of new medical product.

Translation of an idea into a safe and effective marketed product requires integrated knowledge from several areas. BEC’s strong vision, engineering experience, knowledge of use factors, and practice in the regulatory compliance landscape ensure that the progression from early stage to marketed product is appropriately planned and executed with high quality and financially cost effective goals.