eClinPro CTMS & eSource
Who Is the Company Behind eClinPro CTMS & eSource?
- Seller: eClinPro
- Year Founded: 2020
- HQ Location: Hialeah, US
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LinkedIn® Page: www.linkedin.com
6 employees on LinkedIn®
Total Products under this Category: 220
Last updated: November 01, 2026
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Highlighted products: OnCore CTMS, Viedoc, Clinical Research Suite, Florence eBinders, Rave CTMS, Clario CTMS, Vial EDC + eSource, and TrialKit.
Underlying data: [Grid® JSON](https://www.g2.com/categories/clinical-trial-management-systems/grids.json?focus%5B%5D=oncore-ctms&focus%5B%5D=viedoc&focus%5B%5D=clinical-research-suite&focus%5B%5D=florence-healthcare-florence-ebinders&focus%5B%5D=rave-ctms&focus%5B%5D=clario-ctms&focus%5B%5D=vial-edc-esource&focus%5B%5D=trialkit)
With our strong continuation capabilities, Taimei Technology CTMS (eCooperate) can seamlessly integrate into your existing processes and workflows, allowing you to customize the system to fit your unique needs. Whether you're managing a single-site study or a complex, multi-site trial, our platform can be tailored to your specific requirements.
Connect G2 to Claude or ChatGPT for answers grounded in G2's trusted reviews, comparisons, and pricing from real user insights.
EDGE is an innovative cloud-based research management system created by the Clinical Informatics Research Unit at the University of Southampton.
elsai Clinical Protocol Audit Agent helps sponsors, CROs, regulatory affairs teams, compliance specialists, and medical writers review clinical study documents with greater consistency, traceability, and control. The agent evaluates protocols, informed consent forms, recruitment materials, and other clinical study documents against configurable validation and compliance rules. Instead of returning unsupported findings, every issue must be backed by exact source text from the document. If supporting evidence cannot be verified, the finding is excluded. For each validation rule, the agent identifies the relevant section, verifies the underlying evidence, determines whether the document meets the requirement, explains the reasoning, and provides a confidence score. Where appropriate, it can also recommend corrected or replacement text for human review.
Intelligent Engineering for Clinical Trial Management Improve management and oversight of your clinical trials. Engility® supports rapid implementation and evolution with a highly intuitive user interface to increase adoption. Engineered for change, our continuous validation model enables your agility and journey towards unified trial governance.
A Comprehensive Solution to Capture and Manage Clinical Trial Information. The Ennov Clinical suite consists of Clinical Data Management applications (EDC, RTSM and ePRO) as well as Clinical Trial Management applications (CTMS and eTMF) that are available for deployment in the cloud or on premises
eClinical is the next-generation self-configurable clinical trial workflow management solution site feasibility and selection, study start-up, training/certification, safety alert management, remote monitoring, patient recruitment and eTMF.
Evado OnDemand is a cloud-based clinical trial management platform designed to streamline the setup and execution of clinical trials, studies, and registries. Developed and hosted in Australia, it offers a fully integrated environment that allows sponsors to run multiple trials across various sites efficiently. The platform is accessible via standard web browsers and mobile devices, ensuring flexibility and ease of use. Key Features: - Scalability: Supports an unlimited number of trials and studies simultaneously within a single environment. - Data Collection Tools: Provides online form tools for efficient data collection, including case report forms, questionnaires, and standardized data collection instruments. - Regulatory Compliance: Meets regulatory requirements such as FDA Part 11, HIPAA, and the Code of Good Clinical Practice 6. - Flexible Service Tiers: Offers three tiers of service—Lite, Standard, and Enhanced—to cater to trials of varying sizes, from small studies with up to 200 subjects to large registries exceeding 500 subjects. - Remote Capabilities: Enables remote trial participation and monitoring, facilitating decentralized clinical trials. - Integrated Informed Consent: Features electronic informed consent, which can function as a standalone module or be integrated with electronic data capture . Primary Value: Evado OnDemand addresses the need for rapid deployment and management of clinical trials, especially in scenarios requiring immediate access to clinical software. By offering a cloud-based, scalable, and compliant platform, it simplifies trial record management, accelerates the setup-to-recruitment timeline, and ensures data integrity. This solution is particularly beneficial for sponsors seeking a cost-effective and efficient method to conduct clinical research without the delays associated with traditional trial setups.