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The Ins and Outs of CTMS Data Migration
[Session #]
[Date]
Param Singh
Vice President of
Clinical Trial Management Solutions
BioPharm Systems, Inc.
1
Today’s Agenda
Topic
Welcome and Introductions
Should We Migrate?
What Should We Migrate?
How Should We Migrate?
When Should We Migrate?
Migration Demo
Q&A
Should We Migrate? (Purpose)
• What are the benefits of having historical
study data in the new CTMS?
– Comprehensive reporting
– Complete picture of each study
• What are the benefits of having current
study data in the new CTMS?
– All study team members working in one
system within one set of business processes
– More cost-effective for IT to support and
maintain one system
3
Should We Migrate? (Purpose)
• What are the risks of migrating?
– Loss of Functionality: New CTMS might not
have the same functionality as all combined
legacy systems and tools
– Loss of Data: Data could be lost in the
process of cleaning and/or migrating
– Time Lag: Could be a gap between when the
data is unavailable in the legacy system and
when it is available in the new system
– Time Overlap: One study could be available
in two systems before the legacy system is
decommissioned
4
Examples Scenarios
Growing CRO
• Recently secured a new,
global client
• Several large-scale and long-
term studies planned or
already started
• Limited human resources to
manage studies; need to
operate as efficiently as
possible
• Limited IT department to
support systems and tools
Global Pharma
• For all studies of all sizes,
need to track subject data,
even after officially closed
• New Clinical Director
requires comprehensive
reporting on study, site, and
vendor expenses
• Recently implemented a data
warehouse
What Should We Migrate? (Scope)
• Scoping takes place on two levels:
1. Study: Which studies should be migrated?
2. Data Type: Which types of data should be migrated for all of the studies
chosen?
• Begin with a study-by-study analysis:
– Compare each study timeline to your CTMS implementation timeline,
especially CTMS go-live date and legacy system cutoff date(s)
– For current studies, consider the volume of work that remains, given
available resources
6
Example Studies
EndSoon Study LastLong Study StartSoon Study
Study ends in three
months (before legacy
system cutoff)
Study will continue for at
least one year post CTMS
go-live
Study begins one month
before CTMS go-live
Manageable volume of
work with available staff
Large volume of work Moderate volume of
work, but do not need to
use CTMS for first 2
months
Migrate = No Migrate = Yes Migrate = No
7
What Should We Migrate? (Scope)
• Data Types: Which are available in the new CTMS?
– Contacts – Subject Visits
– Accounts – Adverse Events
– Addresses – Protocol Deviations
– Products – Correspondence
– Programs/Projects – Site Visit Reports
– Studies – Investigator Payments
– Sites – Vendor Expenses
– Subjects – Documents
8
What Should We Migrate? (Scope)
• Which are you currently tracking?
– Contacts – Subject Visits
– Accounts – Adverse Events
– Addresses – Protocol Deviations
– Products – Correspondence
– Programs/Projects – Site Visit Reports
– Studies – Investigator Payments
– Sites – Vendor Expenses
– Subjects – Documents
9
What Should We Migrate? (Scope)
• Which of the remaining data types do you need in the system
going forward? Think:
– Extracting and/or reporting data
• No need for correspondence; no reporting needs
• No need for adverse events; safety system is system of record
– Acceptable workarounds
• Keeping existing vendor payments tool
• Approved site visit reports can be printed and archived
10
How Should We Migrate? (Methods)
• Inventory your source systems: Where
does the data currently live?
– Spreadsheets
– MS Access databases
– Home-grown databases
– Word documents
– Document management system
– Accounts payable system
– Existing CTMS
11
How Should We Migrate? (Methods)
• How many records do you have of each
date type in each source system?
– Use reports or embedded functions that
provide row and column counts
• How closely does the source system
format map to the CTMS format? Think:
– Relationships: one-one, one-many, many-
many
– Attributes: fields
– Data Standards: field contents
12
How Should We Migrate? (Methods)
• Manual migration vs. automated
migration
– Automated options:
• Embedded tools
• Existing external tools
• Custom-built tools
• To choose a method, consider:
– Available tools – Available
staff
– Volume – Complexity
– Budget – Time
13
When Should We Migrate? (Timing)
• Timing depends on your CTMS rollout strategy
– Big Bang: All studies go live at the same time
– Study-by-Study: Begin with a pilot study, roll out subsequent studies one
by one
• Recommendation: Study-by-Study
– Iron out kinks in business processes and training materials during pilot
• Increases user adoption
– Easier to manage training rollout
14
Summary
4 Phases of CTMS Data Migration Analysis
• Purpose: What is the business driver behind the
migration?
• Scope: Which studies do we need? Which data
types do we need for those studies? How will
the data be used?
• Methods: What tools and resources are
available, and how do they fit with our budget
and timeline?
• Timing: What makes the most sense,
considering our CTMS rollout plan?
15
Q&A
16
Closing
Thank you for attending!
psingh@biopharm.com
+1 877-654-0033
+44 (0) 1865 910200
17
Presenter Bio
Param Singh
Vice President of
Clinical Trial Management Solutions
• 5+ years with BioPharm
• 13+ years of experience
implementing Siebel Clinical
• 30+ Siebel Clinical implementations
18

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2013 OHSUG - The Ins and Outs of CTMS Data Migration

  • 1. The Ins and Outs of CTMS Data Migration [Session #] [Date] Param Singh Vice President of Clinical Trial Management Solutions BioPharm Systems, Inc. 1
  • 2. Today’s Agenda Topic Welcome and Introductions Should We Migrate? What Should We Migrate? How Should We Migrate? When Should We Migrate? Migration Demo Q&A
  • 3. Should We Migrate? (Purpose) • What are the benefits of having historical study data in the new CTMS? – Comprehensive reporting – Complete picture of each study • What are the benefits of having current study data in the new CTMS? – All study team members working in one system within one set of business processes – More cost-effective for IT to support and maintain one system 3
  • 4. Should We Migrate? (Purpose) • What are the risks of migrating? – Loss of Functionality: New CTMS might not have the same functionality as all combined legacy systems and tools – Loss of Data: Data could be lost in the process of cleaning and/or migrating – Time Lag: Could be a gap between when the data is unavailable in the legacy system and when it is available in the new system – Time Overlap: One study could be available in two systems before the legacy system is decommissioned 4
  • 5. Examples Scenarios Growing CRO • Recently secured a new, global client • Several large-scale and long- term studies planned or already started • Limited human resources to manage studies; need to operate as efficiently as possible • Limited IT department to support systems and tools Global Pharma • For all studies of all sizes, need to track subject data, even after officially closed • New Clinical Director requires comprehensive reporting on study, site, and vendor expenses • Recently implemented a data warehouse
  • 6. What Should We Migrate? (Scope) • Scoping takes place on two levels: 1. Study: Which studies should be migrated? 2. Data Type: Which types of data should be migrated for all of the studies chosen? • Begin with a study-by-study analysis: – Compare each study timeline to your CTMS implementation timeline, especially CTMS go-live date and legacy system cutoff date(s) – For current studies, consider the volume of work that remains, given available resources 6
  • 7. Example Studies EndSoon Study LastLong Study StartSoon Study Study ends in three months (before legacy system cutoff) Study will continue for at least one year post CTMS go-live Study begins one month before CTMS go-live Manageable volume of work with available staff Large volume of work Moderate volume of work, but do not need to use CTMS for first 2 months Migrate = No Migrate = Yes Migrate = No 7
  • 8. What Should We Migrate? (Scope) • Data Types: Which are available in the new CTMS? – Contacts – Subject Visits – Accounts – Adverse Events – Addresses – Protocol Deviations – Products – Correspondence – Programs/Projects – Site Visit Reports – Studies – Investigator Payments – Sites – Vendor Expenses – Subjects – Documents 8
  • 9. What Should We Migrate? (Scope) • Which are you currently tracking? – Contacts – Subject Visits – Accounts – Adverse Events – Addresses – Protocol Deviations – Products – Correspondence – Programs/Projects – Site Visit Reports – Studies – Investigator Payments – Sites – Vendor Expenses – Subjects – Documents 9
  • 10. What Should We Migrate? (Scope) • Which of the remaining data types do you need in the system going forward? Think: – Extracting and/or reporting data • No need for correspondence; no reporting needs • No need for adverse events; safety system is system of record – Acceptable workarounds • Keeping existing vendor payments tool • Approved site visit reports can be printed and archived 10
  • 11. How Should We Migrate? (Methods) • Inventory your source systems: Where does the data currently live? – Spreadsheets – MS Access databases – Home-grown databases – Word documents – Document management system – Accounts payable system – Existing CTMS 11
  • 12. How Should We Migrate? (Methods) • How many records do you have of each date type in each source system? – Use reports or embedded functions that provide row and column counts • How closely does the source system format map to the CTMS format? Think: – Relationships: one-one, one-many, many- many – Attributes: fields – Data Standards: field contents 12
  • 13. How Should We Migrate? (Methods) • Manual migration vs. automated migration – Automated options: • Embedded tools • Existing external tools • Custom-built tools • To choose a method, consider: – Available tools – Available staff – Volume – Complexity – Budget – Time 13
  • 14. When Should We Migrate? (Timing) • Timing depends on your CTMS rollout strategy – Big Bang: All studies go live at the same time – Study-by-Study: Begin with a pilot study, roll out subsequent studies one by one • Recommendation: Study-by-Study – Iron out kinks in business processes and training materials during pilot • Increases user adoption – Easier to manage training rollout 14
  • 15. Summary 4 Phases of CTMS Data Migration Analysis • Purpose: What is the business driver behind the migration? • Scope: Which studies do we need? Which data types do we need for those studies? How will the data be used? • Methods: What tools and resources are available, and how do they fit with our budget and timeline? • Timing: What makes the most sense, considering our CTMS rollout plan? 15
  • 17. Closing Thank you for attending! psingh@biopharm.com +1 877-654-0033 +44 (0) 1865 910200 17
  • 18. Presenter Bio Param Singh Vice President of Clinical Trial Management Solutions • 5+ years with BioPharm • 13+ years of experience implementing Siebel Clinical • 30+ Siebel Clinical implementations 18