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- Easy Study Build Process: Several users have found the study build process relatively easy to learn and navigate, allowing them to …
Merative Clinical DevelopmentFormerly IBM Clinical Development / Watson Health
Overview
What is Merative Clinical Development?
IBM Clinical Development (formerly eClinicalOS) is a cloud-based electronic data capture (EDC) system.
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What is Merative Clinical Development?
IBM Clinical Development (formerly eClinicalOS) is a cloud-based electronic data capture (EDC) system.
Entry-level set up fee?
- Setup fee optional
For the latest information on pricing, visithttps://www.ibm.com/products/clinical…
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- Free Trial
- Free/Freemium Version
- Premium Consulting/Integration Services
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Product Details
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- Integrations
- Competitors
- Tech Details
- Downloadables
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What is Merative Clinical Development?
Merative® Clinical Development (formerly IBM® Clinical Development) is a unified, cloud-based Clinical Data Management System designed to help reduce the cycle time to start, amend, and manage clinical studies — enabling life sciences organizations to deliver therapies and innovations faster to their patients.
Boasting a proven track record of over 3000+ clinical trials, in 90+ countries, with 1 million+ participants, the vendor states Merative® Clinical Development will help pharmaceutical, medical device, and CROs to shorten study cycle time and reduce costs.
In addition to its core electronic data capture (EDC) functionality, Merative® Clinical Development offers a fully-integrated portfolio of modules that are designed to suit every trial, including:
Medical Coding with AI- Designed to increase efficiency by leveraging AI to build consistency and reduce errors
eConsent - Deliver quick and easy remote participant consenting without additional EDC integration
Open Platform Data Integration - Allows users to build and automate data connectors with minimal coding
Reporting and Analytics - Provide Data Managers to use pre-built or custom reports to derive single and cross-study insights
Electronic Clinical Outcome Assessment (eCOA) - Strengthens Participant Centricity with live, automatic data sync with EDC
Visit https://www.merative.com/clinical-development to learn more.
Boasting a proven track record of over 3000+ clinical trials, in 90+ countries, with 1 million+ participants, the vendor states Merative® Clinical Development will help pharmaceutical, medical device, and CROs to shorten study cycle time and reduce costs.
In addition to its core electronic data capture (EDC) functionality, Merative® Clinical Development offers a fully-integrated portfolio of modules that are designed to suit every trial, including:
Medical Coding with AI- Designed to increase efficiency by leveraging AI to build consistency and reduce errors
eConsent - Deliver quick and easy remote participant consenting without additional EDC integration
Open Platform Data Integration - Allows users to build and automate data connectors with minimal coding
Reporting and Analytics - Provide Data Managers to use pre-built or custom reports to derive single and cross-study insights
Electronic Clinical Outcome Assessment (eCOA) - Strengthens Participant Centricity with live, automatic data sync with EDC
Visit https://www.merative.com/clinical-development to learn more.
Merative Clinical Development Screenshots
Merative Clinical Development Integrations
- BSI CTMS
- Veeva Clinical Platform
- Argus
- Transperfect
- ALMAC
- Fisher
- Medable
- TRI
- CluePoints
- Catalent
- Optum
Merative Clinical Development Competitors
Merative Clinical Development Technical Details
| Deployment Types | Software as a Service (SaaS), Cloud, or Web-Based |
|---|---|
| Operating Systems | Unspecified |
| Mobile Application | Apple iOS, Android, Windows Phone, Blackberry, Mobile Web |
| Supported Countries | Worldwide usage |
| Supported Languages | 50 + languages and dialects |
Merative Clinical Development Downloadables
Frequently Asked Questions
IBM Clinical Development (formerly eClinicalOS) is a cloud-based electronic data capture (EDC) system.
Medidata Rave EDC, Veeva Vault PromoMats, and Medrio are common alternatives for Merative Clinical Development.
Reviewers rate Support Rating highest, with a score of 8.6.
The most common users of Merative Clinical Development are from Mid-sized Companies (51-1,000 employees).
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Reviews and Ratings
(33)
Community Insights
TrustRadius Insights are summaries of user sentiment data from TrustRadius reviews and, when necessary, 3rd-party data sources. Have feedback on this content? Let us know!
- Pros
- Cons
- Easy Study Build Process: Several users have found the study build process relatively easy to learn and navigate, allowing them to quickly create studies. The availability of tools within the system has been praised for assisting builders throughout the process.
- Excellent Support: Many reviewers highly appreciate the outstanding support provided by the technical helpdesk and project management teams, which has been instrumental in their success with the system.
- Dedicated Client Success Manager: Users value having their own Client Success Manager who provides excellent guidance and assistance throughout their experience with the system. The specific mention of a user's Client Success Manager doing an excellent job highlights this positive aspect.
Slow response to suggestions/issues: Some users have expressed frustration with the slow response from the system's support team when it comes to addressing suggestions or issues related to enhancing the system functionalities.
Non-standard functionalities require additional payments: Several reviewers have mentioned that certain functionalities in the system are not included in the standard package and require additional payments, which can be a disadvantage for some users.
Expensive certification in certain modules: The cost of certification in certain modules, such as Data Migrator, has been highlighted by a number of users as being expensive, making it less accessible for individuals or companies on a tight budget.
Attribute Ratings
Reviews
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February 19, 2021
Clinical Database Designing Made Easy
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.
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
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.
- Implemented in-house
No
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.
I do not think so.
No
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.
- eCRF importing
- Study importing
- MSU process
- Inviting users to studies
- User management
Yes
Wonderful. Screen scalability is excellent!