Research Affairs would like to invite you to the March 14 Noontime Seminar:
ClinicalTrials.gov: An Overview for Principal Investigators and Clinical Research Staff
Human subjects protections training, research conflict of interest training and disclosure, IRB application…
As human subjects researchers, you have come to learn that these are among the few specific, unavoidable regulatory requirements that are just part of getting the job done. If your research includes performing clinical trials (broadly defined!), then one other BIG, non-optional requirement is part of the list: ClinicalTrials.gov.
This public, online registry of clinical trials and their results, hosted by the Federal Government, is the subject of this month’s important presentation. If you:
- Want to publish results of your study
- Secure NIH funding
- Avoid ridiculous potential fines (technically, as high as $10,000 per day! )
then you need to be well-versed in how to assure your study is compliant with existence of, mechanics of, and rules that require your study to be listed on the ClinicalTrials.gov website.
Jerri’s presentation to day will smooth the path for those of you unfamiliar with this, and will substantially broaden the knowledge and skills for those of you who already know about the registration system.
Join us for tasty sandwiches and an hour well-spent. Pre-registration required.
The seminar will be held in the Research Affairs main conference room from 12-1pm. Physicians attending this session will earn CME.
You must register to receive credit and so we can have lunch ready for you.
Please click link to Register
NOTE: If you do register, please make every effort to attend, or contact us in advance, if you can, should your plans change. Seating is limited and we do maintain a waiting list. That will allow us to give you “ticket” to one of your research colleagues.
Thank you for your attention. We look forward to seeing you there.