Press Releases
Clinical Trial Risk Management Seminar
SAN FRANCISCO, CA, UNITED STATES - May 21, 2019 - ExL Events extends its well-known and established clinical quality series of events to the West Coast with the Clinical Trial Risk Management Seminar. Click here to view the detailed program.
To register, click here and use Priority Code 783819CRN. Budget-friendly, two-day and one-day rates are available.
The event features four half-day sessions, each exploring a specific topic through an interactive session, providing you with a solid understanding of critical elements, followed by a panel of industry experts sharing their experiences on the subject.
The four topics include:
THE IMPACT OF ICH E6 R2
Break Down the Critical Elements of ICH E6 R2 and Their Impact on Clinical Operations
Pam Dellea-Giltner, B.D., MBA, CCRA, President, PDG CLINICAL CONSULTING, LLC
CLINICAL RISK MANAGEMENT
Unlock the Secrets of a Successful Clinical Risk Management Process
Todd Johnson, Principal Consultant, Organizational Solutions, HALLORAN CONSULTING GROUP
Sheila Gwizdak, Principal Consultant, Quality, HALLORAN CONSULTING GROUP
CRO OVERSIGHT
Understand the Impact of ICH E6 R2 on the Requirements for Sponsors and CROs Related to Oversight
Liz Wool, President, WOOL CONSULTING GROUP, INC.
CLINICAL INSPECTION READINESS
Create a Preparation Plan That Guides All Stakeholders to Achieve a Constant and Confident State of Inspection Readiness
Michele Weitz, Senior Director, GCP Compliance Operations, CLOVIS ONCOLOGY
For more information on available sponsorship and exhibition opportunities, please contact Arthur Butler at 917-932-0429 or abutler@exlevents.com.
For all other questions and comments, please contact Kristen Hunter at khunter@exlevents.com or 212-400-6241.
