On-Demand Webinar: Clinical Trial Agreements - Addressing Frequently Asked Questions
Presented by Ryan Meade
As a follow up to the popular Clinical Trial Agreement (CTA) webinar, Ryan Meade, from Aegis Compliance & Ethics Center will return to answer some of the viewers' questions from that webinar in this FAQ format webinar. In his first webinar, Ryan discussed language used in CTAs that can cause billing problems, what happens when the study team misinterprets the sponsor's budget, and how sponsor payments for subject stipends can have a ripple effect on billing.
A lot of great content resulted in many questions that we didn't have time to address. Join us for this webinar to learn more about CTAs and what you can do to avoid any financial implications at your site.
Some sample questions include:
- What are the OIG Advisory Opinions addressing waiving a research subject’s co-pays?
- Where do subject stipends stand under federal law?
- How do we establish what is fair market value for research work we are doing for a sponsor?
- Is there a problem with different sponsors paying different rates for the same service?
Previously Recorded: May 27, 2015
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