Rating
5.0
1 reviews
Categories
1
Founded
2011
Employees
67
Flex CTMS is a compliant Clinical Trial Management System designed for life sciences organizations to manage studies from start-up through close-out. Key Features: Study & Site Management: Plan studies, track milestones, manage sites and investigators. Subject & Visit Tracking: Monitor enrollment, visits, and participant data. Financial Management: Budgeting, invoicing, and cost tracking. Real-Time Reporting: Dashboards and reports for study progress, timelines, and finances. Compliance & Security: Role-based access, full audit trails, 21 CFR Part 11 and GxP validated. Integrated Platform: Shares data with EDC, eTMF, QMS, and PV modules for a single source of truth. Benefits: Streamlines trial operations, reduces manual work, improves data integrity, ensures regulatory compliance, and scales across studies and portfolios for CROs, pharma, biotech, and academic research.
Ad spend / mo
$8K
44 paid keywords
Paid visits / mo
983
Organic keywords
673
Organic visits / mo
285
Authority
25
449 ref domains
Creatives run
25
as Flex Databases s.r.o.
Active now
6
last 14 days
Advertising since
Dec 2021
4+ yrs running
Last seen
2d ago
still active
(1 reviews)
We found FDB to be a very intuitive and user-friendly system. Compared to our previous solution, FDB saves us time and makes it much easier for the CRAs to efficiently handle all tracking and reporting tasks.
Pros: The system offers data import tools that allow users to update certain reports simply by uploading an updated Excel file, and you can build your own transversal reports easily. Video tutorials are also available within the system, enabling users to train themselves on their specific tasks at their own pace. We would rate FDB's customer service as exceptional, and this was one of the main reasons we chose FDB over other providers. In addition, a support email is available to address any daily issues, and any incidents are always resolved quickly.
Cons: Although the system doesn't require a dedicated administrator role, configuring certain reports and tracking templates can take some time, as you need to apply the necessary updates. The configuration is generally quite flexible, but it doesn't allow changes to templates that have already been published. However, keeping track of template updates is simple and straightforward.
Jaume C. · Clinical Trial Manager · Research · December 16, 2025
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Domain confidence 95%
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Clinical Research Software
Flex Databases — eClinical system for Sponsors, CROs, Academic companies. CTMS, EDC, eTMF. Manage studies, sites, documents and data in one platform.
https://www.flexdatabases.com
Clinical Trial Management
All in One CTMS — CRA Activity Management. Subject Tracking & Invoicing. Investigators & Sites Management. Modern CTMS for CROs & Sponsors. Manage sites, subjects, monitoring and TMF in one system.
https://www.flexdatabases.com
Clinical Research Software
CTMS, EDC and eTMF integrated — Organize All Information on Investigators and Sites with Investigators & Sites Management. eClinical system for Sponsors, CROs, Academic companies. CTMS, EDC, eTMF. EudraLex compliant.
https://www.flexdatabases.com
Clinical Trial Management
Evidence-Based Decisions — CRA Activity Management. Subject Tracking & Invoicing. Investigators & Sites Management. Evidence-based decisions. More information – less efforts. Build in eTMF. EudraLex compliant.
https://www.flexdatabases.com
Clinical Trial Management
Flex Databases — CRA Activity Management. Subject Tracking & Invoicing. Investigators & Sites Management.
https://www.flexdatabases.com
