Median Technologies
Who Is the Company Behind Median Technologies?
- Seller: Median Technologies
- Year Founded: 2002
- HQ Location: Valbonne, FR
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LinkedIn® Page: www.linkedin.com
203 employees on LinkedIn®
Total Products under this Category: 222
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)
Medigen Suite is Meditrial's eClinical platform for streamlined global clinical operations. Designed as a modular clinical trial software, it supports medical device companies, biotechnology firms, pharmaceutical sponsors, CROs, and academic research institutions across all study phases. - Catchtrial EDC delivers comprehensive electronic data capture with ePRO, eDiary, eConsent, and decentralized trial (DCT) capabilities for seamless patient engagement and remote data collection. - Maptrial CTMS provides full clinical trial management, including site monitoring, study tracking, and operational oversight for efficient trial execution. - Mastertrial LMS+ delivers scalable digital training for investigators and research teams to accelerate site activation and ensure regulatory compliance. Medigen Suite also offers a lightweight, cost-effective configuration for rapid study startup and feasibility assessments, making it accessible for organizations of any size.
CDISC-based fast eCRF production with AI technology. Provides customized EDCs. GAMP5 certification as an integrated platform for clinical trial data management. 21 CFR Part 11, Annex 11 Certification ISO900:2015 Certification 24/7 Global Service Support Team Quick trial start and affordability compared to other systems
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Streamline trial operations and maintain total oversight with an intuitive, audit-ready CTMS built specifically for growing teams. Medrio CTMS gives you a single source of truth for managing key operations. Oversee study startup, site readiness, monitoring visits, and enrollment progress without enterprise cost, added complexity, or burdensome programming.
Patient pre-screening AI assistant for clinical trial recruitment.
An innovative, no-code platform for conducting participant-centric digital clinical trials in record time. Collect eConsent, ePROs, and wearable device data from Fitbit, Garmin, Oura, Apple Watch, Google Fit and more. Connect to EHR and claims records for a more robust longitudinal record of each participant. All data is stored in the HIPAA-compliant, Meaningful Use Certified EDC HIEBus™ platform, and is then exported to researchers in an easy-to-use format, allowing scientists to focus on science.
myLaminin is an enterprise sovereign Clinical Trial Management System (CTMS), Research Data Management (RDM), and Verifiable Credentials platform. Backed by dual USPTO and CIPO patents, AWS Partnership status, and SOC 2 Type II compliance, myLaminin provides full lifecycle trial operations aligned with ICH E6(R3) and 21 CFR Part 11, alongside secure federated data management and institution-agnostic verifiable credentials.
Neuratrial is an advanced clinical intelligence platform designed to streamline and enhance the clinical research process. By integrating a sophisticated reasoning engine with comprehensive biomedical databases, Neuratrial enables researchers to eliminate errors, accelerate compliance, and derive faster insights from complex data. Its enterprise-grade security ensures that sensitive information remains protected throughout the research lifecycle. Key Features and Functionality: - Advanced Reasoning Engine: Facilitates context-aware clinical reasoning by processing multi-modal data and integrating biomedical literature, leading to evidence-based insights and faster decision-making. - Biomedical Databases: Provides access to a centralized knowledge base, allowing researchers to efficiently retrieve and analyze relevant biomedical information. - Enterprise Security: Ensures data privacy through strict data isolation and user-specific encryption keys, preventing data leakage and maintaining compliance with regulatory standards. - Flexible Deployment Models: Offers both self-service subscriptions for individuals and small teams, and custom enterprise deployments for larger organizations, catering to diverse operational needs. Primary Value and User Solutions: Neuratrial addresses the challenges of managing and interpreting vast amounts of clinical data by providing a purpose-built platform that enhances productivity and accuracy in clinical research. It supports faster decision-making, ensures regulatory compliance, and offers scalable solutions tailored to the size and needs of the research team. By leveraging Neuratrial, organizations can accelerate their research timelines, reduce errors, and improve overall outcomes in clinical trials.
OmniStar Ethics is cloud-based research ethics and governance management software for universities and research institutes worldwide, and the hospitals and health services they work with. It runs human, animal, biosafety and gene technology ethics review and research governance in one ready-to-use, flexible platform, from a single application through committee review, approval, amendments, safety reports and final reports. It integrates with HR systems, animal management systems and other corporate systems, so researchers and committees aren’t retyping data. Institutions use OmniStar to replace dated standalone systems and cut the time staff spend re-entering data. Clients include NHMRC, the University of Sydney and Sunway University. OmniStar is ISO 27001 certified, hosts each client’s data in their own region and is assessed to the Australian Government’s IRAP PROTECTED level.