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Dec
7
Adobe Sign and Part 11 Compliance
By Jessica Meyer, MBA, Assistant Manager, Workforce Development, Spectrum

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.  

 

By attending this workshop, you will: 

  • 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

Speaker(s): 

  • Jennifer Brown, RN, Director, Clinical Research Quality, Spectrum (Mar. 17)
  • Anthea Buchin, MS, Manager, IT Research Systems, Technology and Digital Solutions, Stanford Health Care and School of Medicine (Mar. 17, Dec. 7)
  • Todd Ferris, MD, Chief Technology Officer, Technology and Digital Services (Dec. 7) 

Target Audience

Research coordinators, nurses, faculty, staff and post-doctoral scholars working on clinical research projects at Stanford University.