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Up one level The Clinical Trials Transformation Initiative (CTTI) will conduct projects that identify practices with the potential to increase the quality and efficiency of clinical trials. Examples of potential projects include research to evaluate methods or strategies to improve the design or operations of clinical trials; consensus panels or expert meetings to assess current practice or develop recommendations for best practice; and development of models for improvement. The CTTI Executive Committee has established four priority areas for research: design principles, data quality and quantity (includes monitoring), study start-up, and adverse event reporting.
Effective and Efficient Monitoring as a Component of Quality — last modified September 09, 2010 03:32 PM - EST
Workshops on Quality-by-Design in Clinical Trials — last modified December 07, 2011 07:20 AM - EST
Improving Unexpected SAE Reporting to IND Investigators — last modified September 09, 2010 03:32 PM - EST
IND Safety Assessment and Communication — last modified November 21, 2011 05:41 PM - EST
(SAE Follow-on Project)
Improving the Public Interface for Use of Aggregate Data in — last modified August 31, 2011 12:53 PM - EST
Site Metrics for Study Start-Up — last modified September 29, 2010 05:29 PM - EST
Use of Central IRBs for Multicenter Clinical Trials — last modified October 25, 2011 11:31 AM - EST
CTTI Recommendations — last modified May 20, 2011 11:50 AM - EST

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