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Sustainable Solutions for Global Clinical Research Site Documentation
Session Chair(s)
Betsy Fallen, RN
Consultant
BAFallen Consulting LLC, United States
Building an Investigator Portal from the Ground Up: The Decisions, The Pitfalls, and The Lessons Learned
Learning Objective : Define the changing landscape for process and technology options with insight from independent analysis and leading life science companies; Identify potential risks associated with managing documentation requirements on large global late phase programs; Recognize the special considerations for implementing and integrating digital signatures and investigator portals.
Speaker(s)
Digital Signatures 2.0: Current Usage and Landscape in Clinical Operations
Rodd Schlerf
Phlexglobal, United States
Business Development
Building an Investigator Portal from the Ground Up: The Decisions, The Pitfalls, and The Lessons Learned
Sukh Chugh, MBA
Allergan, Inc., United States
Director, R&D Informatics Services
Using Technology and Processes to Effectively Manage Regulatory Documentation Requirements for Late-Phase Clinical Research
Kate Trainor
PAREXEL, United States
Corp VP, Client Delivery
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