Lokavant

While I was at Lightmatter, I worked with Lokavant, a company that manages and tracks clinical drug trials, with a special focus on Serious Adverse Events (SAEs). The FDA defines SAEs as “An adverse event is any undesirable experience associated with the use of a medical product in a patient. The event is serious and should be reported to FDA when the patient outcome is death, hospitalization, disability, permanent damage, birth defects, [etc..].”

I was tasked with both designing and defining the user interface as well as conducting user research using clickable prototypes to gather feedback on the interfaces I had designed.