Human Ability Designs

Human Ability Designs helps our clients optimize user interfaces and achieve human factors regulatory approvals through a systematic engineering approach during the pre- and post-market development process. Human Ability Designs brings extensive experience, commitment to safety, scalable solutions, and regulatory ready deliverables to help you improve the success of your human factors regulatory submissions, processes, in house team expertise, and medical device user interfaces. Led by a biomedical engineer expertly trained in human factors engineering, we join each client team to help your organization develop and bring to market medical products that are safe, effective, usable, and accessible for end users of all abilities. What We Do Through authentic and systematic human factors engineering methods, we help our clients optimize user interfaces and exceed human factors regulatory requirements to obtain human factors regulatory approvals and minimize post-market issues. * HFE/UE Protocol, Report, and Submission reviews * HFE Training for Teams and Organizations * Threshold Analysis * Task and Use-related Risk Analyses * Heuristic and Expert Reviews * Strategic planning and development of HFE processes * and more.