AI TOOL PROFILE
EvidentIQ: eClinical Software for Clinical Research
- Healthcare
- Clinical Trial Management
- Pharmaceutical companies
- Biotech companies
- Contract Research Organizations (CROs)
- Academic research groups
- Medical device companies
Pricing
Pricing was not clearly available from the provided evidence. Buyers should confirm current pricing on the vendor website.
At a glance
- Best for
- Pharmaceutical companies, Biotech companies, Contract Research Organizations (CROs), Academic research groups, Medical device companies
- Key use cases
- Clinical Trial Data Management, Regulatory Compliance Oversight, Real-World Evidence Collection, Medical Device Study Coordination
- Official website
- Visit evidentiq official website
How AI is used
EvidentIQ offers a portfolio of specialized eClinical platforms designed for different stages of clinical research. The company provides several tools, including Dacima for Electronic Data Capture (EDC), Clindex for integrated trial management (EDC, CTMS, and eTMF), and Carenity for patient engagement and real-world evidence collection.
These tools are designed for organizations in the pharmaceutical, biotech, and medical device sectors, as well as contract research organizations (CROs) and academic research groups. The software supports various study types, from first-in-human trials to post-market surveillance.
Buyers can choose platforms based on their requirements for flexibility, integration, or direct patient access. The solutions are browser-based and can be hosted in either private or public cloud environments in the US or Europe.
Buyers should confirm whether Dacima, Clindex, or Carenity aligns with their specific operational requirements, as each serves a different primary function in the research lifecycle.
Key Features
Electronic Data Capture (EDC)
Digital data collection tools for clinical trials, observational studies, and patient registries.
Clinical Trial Management System (CTMS)
Centralized oversight of study progress and structured reporting.
Electronic Trial Master File (eTMF)
Digital document management for trial files and regulatory documentation.
AI-Assisted Tools
Supports AI drug coding for medication standardization and an AI assistant to help site staff with protocol questions.
Regulatory Compliance
Includes built-in GxP and 21 CFR Part 11 controls for audit trails and data integrity.
Drag-and-Drop Study Builder
Interface designed to support study configuration without the need for programming skills.
Use Cases
Clinical Trial Data Management
Using EDC tools to build and manage electronic case report forms (eCRF) for clinical studies.
Regulatory Compliance Oversight
Maintaining study documentation and audit trails within eTMF and CTMS environments.
Real-World Evidence Collection
Engaging patient communities via the Carenity platform to collect patient-reported outcomes and experiences.
Medical Device Study Coordination
Handling datasets from medical devices through an integrated EDC and CTMS platform.
FAQ
What is EvidentIQ used for?
- EvidentIQ provides software for the clinical research lifecycle, specifically for electronic data capture, trial management, and patient engagement.
Is EvidentIQ compliant with clinical regulations?
- The platforms include built-in GxP and 21 CFR Part 11 controls to support regulatory requirements.
Who is this software designed for?
- It is designed for pharmaceutical companies, biotech firms, CROs, and academic research groups.
Source category: Healthcare
Source subcategory: Clinical Trial Management
More tools in Healthcare
Other published listings in the Healthcare category.
More tools in the Clinical Trial Management software type
Related listings that share the same software type for comparison and shortlisting.
