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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)
Rodd Schlerf
Business Development, Phlexglobal, United States
Digital Signatures 2.0: Current Usage and Landscape in Clinical Operations
Sukh Chugh, MBA
Director, R&D Informatics Services, Allergan, Inc., United States
Building an Investigator Portal from the Ground Up: The Decisions, The Pitfalls, and The Lessons Learned
Kate Trainor
Corp VP, Client Delivery, PAREXEL, United States
Using Technology and Processes to Effectively Manage Regulatory Documentation Requirements for Late-Phase Clinical Research
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