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MCC Clinical Trial Site Data Entry Study
MCC Clinical Trial Site Data Entry Study

MCC Clinical Trial Site Data Entry Study

Price:$375.00
Member Price (code required): $300
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MCC Item #:SDE2016

Clinical Trial Site Data Entry Study 


Report Length:  32 pages
Non-Member Price: $375
Member Price: $300 (see MCC Member Page or contact MCC)

With the adoption of the ICH E6 (R2) Addendum and the increasing focus on risk management in clinical trials, the timely data entry by sites following subject visits is becoming more important. Delayed data entry can lead to increased risk both to subjects and the trial. The Metrics Champion Consortium (MCC) conducted an online survey to elicit industry’s perspective on the critical process of data entry by investigative sites after a subject visit. To accomplish this goal, the survey gathered detailed data about the following data entry topics:

  • Importance of Rapid Data Entry
  • Data Entry Cycle Time Calculation
  • Data Entry Cycle Time Expectations
  • Data Entry Cycle Time Experience 
  • Reasons for Data Entry Delays
  • Data Entry Cycle Time Management Strategies
  • Utilization of eSource Systems
  • Relationship Between Data Entry Cycle Times and Data Quality
  • Relationship Between Data Entry Cycle Times and Overall Site Performance
  • Relationship Between Data Entry Cycle Times and LPLV to DBL Cycle Times
The survey contained 28 questions and represents the experiences of 35 respondents at large and small organizations from across the industry. Results should be taken as indicative if not necessarily fully representative of practices across the industry. The rich data gathered in the survey are presented in 20 tables, charts and graphs.

To view additional information visit http://metricschampion.org/sitedataentrystudy/.

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