CAREier is a communication tool that acts as a customer relationship management (CRM) platform for medical devices. We make documented data actionable and connect disparate solution data silos to automate Title 21 compliance as a “Final and Multiple Distributor” against the malleable list of medical devices with required tracking orders from the U.S. Food and Drug Administration (FDA).
We leverage documentation standards that are required by the Office of the National Coordinator (ONC) from the 21st Century Cures Act and information blocking provisions (Sec. 3022) which adopted the United States core data for Interoperability (USCDI) as a standard. This standard outlines the ability to document the Unique Device Identifier(s) for a patient’s Implantable Device(s). This consists of documentation associated to the device identifier (DI) and a production identifier (PI).
By CAREier leveraging Certified EHR Technology requirements that your system already meets to submit to the Centers of Medicare and Medicaid Services (CMS), we are able to automate processes that are heavily manual, if done at all. Finally, there is application and automation driven from workflows that no longer have to be just “check the box.”
Contact Redox to learn how your organization can integrate any of the healthcare products listed here today.