1/26/2016
Date: Jan 28, 2016
Time: 1pm - 2:30pm EDT
Duration: 90 Minutes - Online
Sponsored by Life Science Training Institute
Description:
After the release of the updated guidances and regulatory requirements in the past 6 months. New expectations have been placed on clinical research stakeholders, particularly in the realm of Risk Management. This new focus puts greater responsibility on CROs to improve their vendor selection and oversight processes.
This interactive live session is designed to help you understand how to outline clear responsibilities between CRO and the different stakeholders in order to design, implement and execute effective risk-based vendor strategies. You will be able to build a risk-based assessment tool for CRO management and much more!
For more info contact SAM at samsather@clinicalpathwaysresearch.com.
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