Full course description
This class will introduce researchers to Adobe Sign including an overview of HIPAA and Part 11 regulatory requirements relating to e-signature platforms used in FDA-regulated research.
- Be able to obtain e-signatures on research records that must be compliant with part 11.
- Learn about regulatory requirements for e-signature platforms.
- Be able to identify key procedures that are in place to protect research participant confidentiality.
- Learn how to establish a new group account on Stanford Adobe Sign that is safe for PHI
Jennifer Brown, RN, Director, Clinical Research Quality, Spectrum
Anthea Buchin, MS, Quality & Regulatory Specialist, Clinical Research Quality, Spectrum
Date: Wednesday, May 26
Time: 12:15 - 1:45 pm
Location: Virtual Class. Please return to the course website to save Zoom information.
Clinical Research Operations Program: Elective
Core Competency: Study and Site Management
Research coordinators, nurses, faculty, staff and post-doctoral scholars working on clinical research projects at Stanford University.