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Effective and Efficient Monitoring as a Component of Quality
Workshops on Quality-by-Design in Clinical Trials
Improving Unexpected SAE Reporting to IND Investigators
IND Safety Assessment and Communication
Improving the Public Interface for Use of Aggregate Data in ClinicalTrials.gov
Site Metrics for Study Start-Up
Use of Central IRBs for Multicenter Clinical Trials
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News
Summaries Available - Workshop on Quality-by-Design in Clinical Trials
February 28, 2012 - EST
CTTI Executive Director Authors Paper on Impediments to Clinical Research
February 21, 2012 - EST
New FDA Guidance on Collection of Safety Data
February 10, 2012 - EST
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