Overview: Participants will learn what constitutes a qualified clinical trial and how to conduct a billing risk assessment on a clinical trial study. A sample tool will be provided. Our discussion will also teach participants how to conduct a Medicare coverage analysis and also develop an associated billing spreadsheet.
Why should you Attend: Clinical trials may involve routine and non-routine items and services. Since these may part of a clinical trial, billing rules are different and you need to determine how the costs for treatment/services will be reimbursed. There may be multiple payors, including the sponsor and the patient’s insurer. If you conduct & bill for clinical trials, you must be familiar with billing risks and understand how to conduct a coverage analysis; to ensure that the items and services provided as part of a clinical trial are billed and reimbursed properly.
Areas Covered in the Session:
- Clinical trials routine and non-routine items and services
- Determining billing risk of a clinical trial
- Conducting a billing risk assessment
- Conducting a Medicare coverage analysis
- Developing a billing spreadsheet to ensure proper billing of identified services
Who Will Benefit:
- Clinical trial research team members
- Coders and billers involved with coding/billing clinical trials
- Principal Investigators
- Individuals responsible for ensuring proper billing assignment for clinical trials
- Including Clinical Trials office personnel.
Gail Madison Brown is a registered nurse and an attorney with over 25 years of experience in health care. For the last 15 years she has focused on health care compliance and revenue cycle management operations. Gail’s experience ranges from starting new compliance programs and making improvements to existing programs for physician practices to large health care organizations. Gail also has provided numerous lectures to healthcare providers, executives and professional colleagues.
Gail Madison Brown will develop, implement, and oversee processes, systems, educational programs, and other activities necessary to support and grow clinical trials activities at the UT Health Science Center. The Chief Clinical Trails Officer (CCTO) provides overall strategic leadership in this area including planning, goal setting, and monitoring organizational performance to ensure cost effectiveness and high quality programs.]
Price : $139.00
Phone No: 1-800-385-1607
Event Link: http://bit.ly/Clinical-Trials-may-be-at-Risk-for-Potential
Contact the event managers listed below for more information about how you can participate at the Webinar on Clinical Trials may be at Risk for Potential Fraudulent Billing by Gail Madison Brown (Chief Clinical Trials Officer).
|Conference/Event Dates:||08/17/2016 - 08/17/2016|
|Primary Industry:||Medical Coding & Billing|
|Other Industries:||Clinical Pharmacology, Medical Coding & Billing, Professional Healthcare|
|Audience:||Clinical trial research team members
Coders and billers involved with coding/billing clinical trials
Individuals responsible for ensuring proper billing assignment for clinical trials
Including Clinical Trials office personnel.
|Booth Size||Booth Cost||Available Amenities|
|Marketing Vehicles Allowed:||n/a|
|Other Booth Sizes Available: n/a|
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