Planned reimbursement pathway
How MARKABLE's monthly routine is designed to fit RTM.
Phase 2, not today. MARKABLE is currently a general-wellness platform, not an FDA medical device. RTM billing requires the monitoring tool to legally be an FDA-defined device. What follows illustrates the routine and the running requirements a clinic would meet once MARKABLE is registered as a Class I Software as a Medical Device. It is not billable today, and it is investor and partner material only.
