This two-part workshop starts with the research billing compliance basics and addresses progressively more challenging topics as the sessions go on.  Whether you are new to the industry or a “grizzled veteran” you brush up on the origins of research billing compliance, the “how to” of Coverage Analysis, document synchronization, auditing & monitoring, and even delve into the differences between investigational device trials and pharma.  Sponsors and CROs are encouraged to attend and join the discussions too!