DIA 48th Annual Meeting
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What Should You Put in a Clinical Quality Assurance (CQA) Agreement
Track
:
Track 11: Compliance to Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Quality Assurance (QA)
Program Code:
253
Date:
Tuesday, June 26, 2012
Time:
1:30 PM to 3:00 PM
EST
CHAIR
:
Neil McCullough, PPD, United States
PRESENTER
(S):
JoAnna Brodie, GlaxoSmithKline, United States
Lisa McKay, The Avoca Group Inc., United States Cassandra Kennedy, Quintiles, United States
Description
This session will focus on how to properly develop, organize, and initiate a Clinical Quality Assurance (CQA). Discussions will include examples of content categories, content, and experiences from speakers who have developed and implemented a CQA.
Learning Objectives:
Discuss what a Clinical Quality Assurance agreement (CQA) can and cannot do for the maintenance of regulatory compliance of a clinical trial and high quality clinical data
Identify what information should go into a CQA
Describe experiences and lessons learned by people who have developed and work under a CQA.
Learning Objectives:
Discuss what a Clinical Quality Assurance agreement (CQA) can and cannot do for the maintenance of regulatory compliance of a clinical trial and high quality clinical data
Identify what information should go into a CQA
Describe experiences and lessons learned by people who have developed and work under a CQA.
This session is a part of:
Handout Online
