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Mobile CRAs:
Transforming Clinical Monitoring Processes through Mobile
Technology
Xiu Wei LIM
Head, Innovation Asia
Quintiles East Asia Pte. Ltd
Insert Twitter Handle here
2
The views and opinions expressed in the following PowerPoint slides
are those of the individual presenter and should not be attributed to
Drug Information Association, Inc. (“DIA”), its directors, officers,
employees, volunteers, members, chapters, councils, Communities or
affiliates, or any organization with which the presenter is employed or
affiliated.
These PowerPoint slides are the intellectual property of the individual
presenter and are protected under the copyright laws of the United
States of America and other countries. Used by permission. All rights
reserved. Drug Information Association, Drug Information Association
Inc., DIA and DIA logo are registered trademarks. All other trademarks
are the property of their respective owners.
Disclaimer
3
1) Investigate CRA On-Site Processes to Drive Efficiency though
Mobile Technology
2) Explore if Clinical Monitoring Mobile Applications improve CRA’s
Productivity and Delivery Quality
Objectives
4
1) CRA On- Site Monitoring Time- Map
2) Access CRA delivery: Before & After
a) Quantitative: Task completion time (Median rate of time)
b) Qualitative: Feedback on Task Quality/ Process Efficiency
3) 4 Mobile Applications
Methods
5
Methods- 4 Mobile Applications
6
Results
SDV/IC
31%
IP Acc
10%
Lab Kit
5%
Query
Resolution
18%
Recruitment
16%
ISF
Management
10%
SAE
5%
PD
5%
Calculate patient’s drug
intake compliance.
Calculate & keep track
of patient’s acceptable
& actual visit window
range
Displays if a searched
drug allowed,
prohibited or restricted
for a study.
Produces high quality
scanned documents &
print outs
CRA On-Site
Monitoring
Time Map
Fig 1
7
Results
Total time
saved per
CRA/ Year (H)
Fig 2
0
10
20
Reduce Error
& Process
Variation
CRA oversight
prior to Site-
Visit, Reduce
Error &
Process
Variation
High Quality
Document
Acquisition
Reduce Error
& Multiple
Cross-
Referencing
0.97H
0.06%
3.54H
0.21%
7.76H
0.47%
23.06H
1.38%
Subject
Visit
Scheduler
IP
Calculator
Mobile
Camera
Scanner
Prohibited
ConMed
8
Results
Prohibited
ConMed
activities
Savings with
ConMed App
Fig 3
0
10
20
30
40
50
60
Time to keep
track of
1 subject
Per SMV (pre-
randomized)
(min)
Time to keep
track of
1 subject
Per SMV (post-
randomized)
(min)
Time to revert
site staff call
(min)
Time to setup
Prohibited
ConMed (H)
Current Future
Total time saved per CRA/ year: 23.06H (1.38%)
9
 Usage of Mobile tools can be implemented in Clinical Trials
through identifying large processes.
 Compacting several tools into a single mobile device
Save time
Increase quality- streamline process
Summary & Conclusion
10
Xiu Wei LIM
Head, Innovation Asia
Quintiles East Asia Pte. Ltd
Join the conversation #DIA2016
Thank You

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Mobile CRAs: Transforming Clinical Monitoring Processes through Mobile Technology

  • 1. 1 Mobile CRAs: Transforming Clinical Monitoring Processes through Mobile Technology Xiu Wei LIM Head, Innovation Asia Quintiles East Asia Pte. Ltd Insert Twitter Handle here
  • 2. 2 The views and opinions expressed in the following PowerPoint slides are those of the individual presenter and should not be attributed to Drug Information Association, Inc. (“DIA”), its directors, officers, employees, volunteers, members, chapters, councils, Communities or affiliates, or any organization with which the presenter is employed or affiliated. These PowerPoint slides are the intellectual property of the individual presenter and are protected under the copyright laws of the United States of America and other countries. Used by permission. All rights reserved. Drug Information Association, Drug Information Association Inc., DIA and DIA logo are registered trademarks. All other trademarks are the property of their respective owners. Disclaimer
  • 3. 3 1) Investigate CRA On-Site Processes to Drive Efficiency though Mobile Technology 2) Explore if Clinical Monitoring Mobile Applications improve CRA’s Productivity and Delivery Quality Objectives
  • 4. 4 1) CRA On- Site Monitoring Time- Map 2) Access CRA delivery: Before & After a) Quantitative: Task completion time (Median rate of time) b) Qualitative: Feedback on Task Quality/ Process Efficiency 3) 4 Mobile Applications Methods
  • 5. 5 Methods- 4 Mobile Applications
  • 6. 6 Results SDV/IC 31% IP Acc 10% Lab Kit 5% Query Resolution 18% Recruitment 16% ISF Management 10% SAE 5% PD 5% Calculate patient’s drug intake compliance. Calculate & keep track of patient’s acceptable & actual visit window range Displays if a searched drug allowed, prohibited or restricted for a study. Produces high quality scanned documents & print outs CRA On-Site Monitoring Time Map Fig 1
  • 7. 7 Results Total time saved per CRA/ Year (H) Fig 2 0 10 20 Reduce Error & Process Variation CRA oversight prior to Site- Visit, Reduce Error & Process Variation High Quality Document Acquisition Reduce Error & Multiple Cross- Referencing 0.97H 0.06% 3.54H 0.21% 7.76H 0.47% 23.06H 1.38% Subject Visit Scheduler IP Calculator Mobile Camera Scanner Prohibited ConMed
  • 8. 8 Results Prohibited ConMed activities Savings with ConMed App Fig 3 0 10 20 30 40 50 60 Time to keep track of 1 subject Per SMV (pre- randomized) (min) Time to keep track of 1 subject Per SMV (post- randomized) (min) Time to revert site staff call (min) Time to setup Prohibited ConMed (H) Current Future Total time saved per CRA/ year: 23.06H (1.38%)
  • 9. 9  Usage of Mobile tools can be implemented in Clinical Trials through identifying large processes.  Compacting several tools into a single mobile device Save time Increase quality- streamline process Summary & Conclusion
  • 10. 10 Xiu Wei LIM Head, Innovation Asia Quintiles East Asia Pte. Ltd Join the conversation #DIA2016 Thank You