Information Session on Availability of the FDA-compliant (“Part 11 compliant”) version of DocuSign: Tuesday March 23rd
What is happening?
The UCSF IT Cloud Content Application group will host an information session to introduce UCSF’s new version of DocuSign which is compliant with the FDA’s privacy rules at 21 CFR Part 11 for electronic signatures. Topics to be covered include:
- Differences between the “regular” version of DocuSign and the new FDA-compliant version of DocuSign
- Determining whether you need to use the FDA-compliant version of DocuSign for obtaining electronic consent
- How to request access to the FDA-compliant version
- Best practices when using the FDA-compliant version
When and where?
Tuesday, March 23rd from 1:00-2:00.
Join the Zoom here at the time of the session, or view a recording of the session at https://it.ucsf.edu/service/electronic-signature-docusign. Please allow a few days for the recording to be posted online.
Who should attend?
- Research personnel of FDA-regulated studies conducting/needing to conduct remote signed consent
- Research personnel conducting/needing to conduct remote consent who are unsure whether their study is subject to the FDA’s privacy rules at 21 CFR Part 11 and/or whether signed consent is required
For more information about this session, please contact the UCSF IT Cloud Content Application group at [email protected].