I would like to quantify my risk.

Required if you anticipate billing routine care costs to Medicare.

Should I bill the office visit to the study or to the patient?

Required for Category B IDEs, some Category A IDEs, Carotid Artery Stenting (CAS) Post-Approval/Post-Approval Extension Studies, and Post-Approval Extension Studies Using 510k-Cleared Embolic Protection Devices (EPDs).

We offer a variety of services and tools to keep you in compliance.

Research Billing Compliance

NEWS

Mandatory Reporting of Clinical Trial Number on Claims


Are your clinical research facilities ready? "Mandatory Reporting of an 8-Digit Clinical Trial Number on Claims" begins effective January 1, 2014. See the attached MLN Matters article 8401 for further details... 
Includes Coverage Analyses, review of claims, and process implementation recommendations.  Customized to your needs.

Should I apply research codes to our study participants' claims?

What is required in order to submit this claim to Medicare?

Delineates who to bill for each test and service at each visit.