Product Overview
EvidentIQ’s CTMS platform streamlines and centralizes the conduct and management of clinical studies in a single, cost-effective system. With its inherent integration with EDC, eCOA, and eTMF, our CTMS offers an enterprise solution to help you make informed and timely decisions.
The comprehensive feature set includes study, site and vendor management, eMonitoring, investigator payments, product management, safety management and a powerful reporting tool.
With the integrated functions to support all the steps in the clinical trial process, an intuitive user interface, and an open architecture to allow users and study administrators to customize their forms and modules, EvidentIQ’s CTMS is the perfect solution to meet your study and business goals.
CTMS software features include IRB/EC, regulatory, and protocol tracking; visit scheduling and compliance; enrollment tracking; product management; comprehensive e-monitoring; site payments; document management system; plus the ability to add features unique to your needs.
Unlike some clinical trial management systems that are created by connecting existing CTMS and EDC systems, Clindex is a single system that offers you all the functionality you need in a single eClinical solution.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Get More Insight Into Your Clinical Trial Management
EvidentIQ’s CTMS facilitates the end-to-end management of clinical trials. The software allows sponsors to be more efficient, make better decisions, ensure compliance, select investigators, monitor patient recruitment and manage finances. Our CTMS includes comprehensive directories to manage site personnel (investigators, sub-investigators, study coordinators, pharmacists) and entities (sites, competent authorities, CROs, suppliers).
Improve site payment cycle time
- Payments are stored and tracked in our payment module
- Support multiple currencies for your global trials
- Payment Requests and Payment Letters to the Investigators can be printed and submitted.
- A detailed history of what was paid is stored for easy reference
- Support tracking accruals
- Identify the amount of payment for each eligible eCRF
- Track what was paid before ensure no double payments
About the company
Leveraging more than 50 years of combined experience providing innovative and creative ways to conduct clinical trials. End-to-end eClinical Solution
Meeting increasing customer demand across clinical operations and clinical data management needs with a suite of applications within a single integrated cloud platform, including EDC, CTMS, eTMF, eCOA, coding, remote monitoring, RBM, RTSM, Payments and eFeasibility. Geographical Reach
In-country patient communities platform in North America and Western Europe (EU5) and ability to conduct studies at a broader scale (LatAM, Asia…). Regulatory expertise to support broader geographical studies.