Signed, Sealed, Delivered: Streamlining Regulatory Processes with eSignatures 

A Complion Feature Article

Streamlining Regulatory with eSignatures - Image

There are many research documents, forms, and agreements that require signature. But when time is spent compiling paperwork and chasing down signatures, Physicians and Coordinators lose precious time.

In this article, Jeremy Rigby of Advanced Clinical Research and Neal Surasky of Chesapeake Research Group share their experience on adopting electronic signatures in the Complion eRegulatory platform. 

Access this article and learn:
  • What are the eSignature adoption trends in clinical research?
  • What does Part 11 say about eSignatures and how do we comply?
  • Are clinical research sites already using e-signatures and how?
  • What are some best practices and lessons learned for staff, physician, and sponsor/CRO adoption?
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