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MCC Clinical Trial Site Data Entry Study
MCC Clinical Trial Site Data Entry Study
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SDE2016
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Description
Customer Reviews
Clinical Trial Site Data Entry Study
Report Length: 32 pages
Non-Member Price: $375
Member Price: $300 (Log into the
MCC Member Site
to access discount pricing)
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
https://metricschampion.org/sitedataentrystudy/
.
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