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Clinical Compliance 2012 - Issue Detection and Escalation in Clinical Trial Settings
Date2012-04-10
Deadline2012-04-10
VenuePalo Alto, USA - United States 
KeywordsClinical Trials; Issue Escalation; Issue Detection; risk mitigation; protocol violations; protocol deviations; IRB qualifications; investigator qualifications; Investigator responsibility
Topics/Call fo Papers
This webinar on issue detection and escalation in clinical trial settings will review the responsibilities of sponsors, investigators, IRB, vendors and CROs in clinical trial setting to maintain compliance.
Why Should You Attend:
In recent years the FDA has increased the number of clinical sites and trials that have been inspected and audited. The number of investigators under investigation or disqualified has increased. IRBs have been inspected and issued with 483 letters.
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Last modified: 2012-02-24 14:44:32