Please note: All required training modules have not yet been posted to this webpage. Upon availability of the additional required training modules (Regulatory, SAE Reporting, Administration, and Auditing) an RTOG Broadcast notification email will be sent out. An RTOG certification of this training will be awarded when all of the required training modules have been completed.
Please contact RTOGQ&A@acr.org for questions related to module content or if you encounter technical difficulty.
Data Submission (part 1)
Data Submission (part 2)
Study Types/Case Status
Quality of Life/Neurocognitive
RTOG Biospecimen Resource Presentation (no quiz)
RA Session June 2012
Other Presentations (no quiz)
Electronic Data Submission
RTOG Clinical Trials Administration
Serious Adverse Event Reporting