Overall Satisfaction with IBM Clinical Development (ICD)
IBM Clinical Development is being used by the Data Management department to build protocol-specific study databases for capturing clinical trial data. Several DM employees use the platform to build studies. Our clinical department uses the platform to review the data which is entered by the research sites. Our Statistical Programming department uses the data extracted from the platform to develop the standardized data tabulation model to be included for generating tables, listings and figures for inclusion in Clinical Study Reports, which are submitted to the FDA. The platform also helps us manage clinical supplies being shipped from supply depots to clinical sites.
- Study Database design.
- Randomization and trial supply management.
- Electronic data capture.
- Electronic patient reported outcomes.
- eConsent capabilities.
- Advanced data validation logics.
- Design error identification.
- Time savings regarding how long it takes to make an EDC Live.
- Reduced EDC Go Live time by at least half (from 60 days to 30).
- Was able to take an EDC live in 14 days on a few occasions.
- Seamless RTSM IRT integration without adding time to Go Live.
IBM Clinical Development has an easier set-up, maintenance and modifiability. Also, there is a cost saving when using IBM CD for a study as Medidata is very expensive.
Do you think Merative Clinical Development delivers good value for the price?
Yes
Are you happy with Merative Clinical Development's feature set?
Yes
Did Merative Clinical Development live up to sales and marketing promises?
Yes
Did implementation of Merative Clinical Development go as expected?
Yes
Would you buy Merative Clinical Development again?
Yes
Using IBM Clinical Development (ICD)
ICD is used by several branches in my company as follows:
- Data Management: Build EDCs and clean data.
- Statistical Programming: Extract and analyze data.
- IT: Extract data and generate dashboards
- Project Management: View ongoing data collection progress.
- Clinical Team: Source document verify
- Safety Department: Monitor safety aspects of ongoing studies.
9 - We have several team members certified in the Designer, Inventory Dispense, and Data Migration. We also have team members who know how to operate the ePRO and API modules.
- Fast EDC Builds
- ePRO studies
- Migrating data from a separate, rescued database.
- Deploying ePRO on our own purchased devices
- Allowing subjects to bring their own devices for ePRO studies
- Adapting from ePRO only to eCOA
- for eConsent
Evaluating IBM Clinical Development (ICD) and Competitors
Yes - ICD is our preferred EDC platform. Previously we used Medidata Rave and Medrio, We still use Rave and Medrio, but much less.
- Price
- Product Features
- Product Usability
- Product Reputation
- Prior Experience with the Product
ICD helps us win study bids because it is affordable while being incredibly dynamic and adjustable to any size study or design.
I would not.
IBM Clinical Development (ICD) Implementation
- Implemented in-house
Change management was a minor issue with the implementation - Demo of system functionality was a big selling point for us.
- None I was privy to.
IBM Clinical Development (ICD) Support
Pros | Cons |
---|---|
Quick Resolution Good followup Knowledgeable team Problems get solved Kept well informed No escalation required Immediate help available Support understands my problem Support cares about my success Quick Initial Response | None |
I do not think so.
Each time I have an issue, I am helped quickly and professionally. I can tell the support team really cares and is very knowledgeable on the product offerings.
Using IBM Clinical Development (ICD)
Pros | Cons |
---|---|
Like to use Relatively simple Easy to use Technical support not required Well integrated Consistent Quick to learn Convenient Feel confident using Familiar | None |
- eCRF importing
- Study importing
- MSU process
- Inviting users to studies
- User management
Yes - Wonderful. Screen scalability is excellent!