The Medicare Coverage Analysis (The Big Picture)
Carrie A. Hanger, Senior Associate
Smith Moore Leatherwood LLP
View Event Flyer.
Registration Cost: Attendance to meetings is free.
Program Description: The presentation will provide an overview of the why, when, and how of a Medicare Care coverage analysis for clinical research.
Upon completion of the conference, attendees should be able to:
- Understand the why and when of a Medicare coverage analysis
- Understand the general rules for Medicare coverage in the clinical trial context
- Identify when an item or service is covered by Medicare
- Conduct a Medicare coverage analysis
Target Audience: Clinical Research Professionals including: Clinical Research Coordinators, Clinical Research Associates, Investigators, Auditors, Project Managers, Regulatory, Data Managers, Quality Assurance and Clinical Research Administrators
Contact Hours: 1 Contact Hours have been approved for through ACRP. Membership is not required for online registration of contact hours.
Contact Hour Cost:
- $0 Chapter Members
- $15 ACRP Members
- $30 Non-Members
To receive contact hours: Purchase the contact hours separately through ACRP, sign in at the registration desk and attend the program. Log on the ACRP website then “ACRP Learning Portal” to complete the evaluation no later than 30 days following the event and obtain the online certificate. To secure the contact hours the attendee must do all three things – sign in during the conference, purchase the contact hours and complete the evaluations.
Refund Policy: There are no refunds unless the program is cancelled by the chapter before the start of the program.
Level: Intermediate
Speaker Information: Healthcare and biosciences attorney Carrie Hanger focuses on the needs of healthcare providers and entities engaged in clinical and pre-clinical research throughout the U.S. With ten years of experience representing and counseling clients, Carrie provides solutions for issues relating to enrollment and reimbursement, licensure and certification, regulatory and corporate compliance, risk management, and business disputes. She regularly analyzes issues related to clinical and preclinical research and drafts and negotiates clinical research related documents, such as clinical trial agreements and confidentiality agreements.