IQVIA (NYSE:IQV) is a leading global provider of information, innovative technology solutions and contract research services dedicated to using analytics and science to help healthcare stakeholders find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA has approximately 58,000 employees worldwide employees worldwide.

Clinical Ink, a global clinical technology company, offers data certainty from source to submission. Our Lunexis eSource clinical technology and configurable direct data capture, eCOA, ePRO, and eConsent modules a suite of solutions for capturing and integrating electronic data from sites, clinicians, and patients at its source naturally enhance your clinical trial workflow by reducing manual labor, providing anytime, anywhere data access, and saving resources as your trials progress.

UNITY is a web-based platform that integrates the collection of clinical data, of patient-reported outcome measures and the AI-supported extraction of radiographic data into the clinical routine. With UNITY, the planning, monitoring and analysis of clinical trials or post-market monitoring studies can be performed in a cost-effective, transparent and efficient manner while involving all stakeholders via the same platform.

Clinical trial management software that allows businesses to reduce clinical trial time, improve accuracy, drive down costs, and more.

OnCore® Enterprise Research, système complet de gestion de la recherche clinique, prend en charge les opérations centralisées dans les centres médicaux universitaires, les centres de cancérologie et les systèmes de soins de santé. Le système OnCore comprend la gestion de la recherche clinique, la conformité de la facturation, la saisie électronique des données, la gestion des échantillons biologiques, les registres de patients et les intégrations pour l'entreprise de recherche.

Facile à personnaliser et à utiliser, entièrement intégré à IVRS et DSM.

SimpleTrials is a Clinical Trial Management System for Sponsors, CROs and Sites. Plans start at $124/month with no long term commitment! SimpleTrials is a validated CTMS and eTMF, including features to support site and contact management, study startup, study planning, contracts and payments, subjects, monitoring and electronic visit reports. SimpleTrials is brought to you by Trial By Fire Solutions, the clinical software provider who has been focused on CTMS and eTMF since 2008.

Le logiciel de gestion des essais cliniques BioClinica CTMS intègre naturellement les outils, flux de travail de processus métier et documents Office dans votre environnement réglementé.

User-friendly software designed for recording and analysing animal tracking within an IR actimeter.

Catchtrial is a simple, cloud-based platform for capturing clinical trial data and images. Accessible anytime, anywhere, Catchtrial puts key information at your fingertips, resulting in shorter response times, improved compliance, and reduced costs.

Système de gestion de données cliniques avec une création d'études simplifiée et de reporting détaillé.

MAISi, l'application d'Agile Health Computing, est un système de gestion d'essais cliniques convivial et sophistiqué, conçu pour répondre aux besoins de gestion des sites de recherche clinique. En collectant et en surveillant les métriques commerciales des sites de recherche, MAISi facilite une meilleure mise en œuvre des protocoles et une meilleure gestion du temps et des finances, ce qui est essentiel dans ce marché international concurrentiel.

MedSciNet est une entreprise basée à Stockholm spécialisée dans la conception et le développement d'applications web et de systèmes de bases de données en ligne pour les essais et études cliniques, les registres de qualité, les biobanques médicales et d'autres solutions dans le domaine médical. Ses bureaux se situent à Londres (Royaume-Uni), Vilnius (Lituanie), Stockholm (Suède) et Cork (Irlande).

Data MATRIX is a company providing full-service data management services based on the in-house developed EDC/IWRS software. Our EDC/IWRS has been used in more than 150 international trials and data were successfully submitted to EMA and FDA. Our user-friendly software are fully validated and meet all the industry standards (CDISC, 21 CFR Part 11).

secuTrial est une puissante solution logicielle web pour les essais cliniques. La conformité totale aux normes BPC et FDA 21 CFR Part 11 est assurée tout en garantissant les normes de qualité les plus élevées. secuTrial offre une grande liberté de conception en matière de conception d'étude, de flexibilité et de convivialité. Il peut donc être utilisé de différentes manières pour toutes les phases d'essais cliniques, comme ceux pour la licence d'homologation ou les études de phase IV.

myClin provides you with the best documented, data-driven clinical trial oversight. It lets your clinical study team collaborate and communicate accessing training, distributing essential documents and tracking study milestones in a central, secure, and private environment.

Designed and developed with the latest technologies Clinicubes CTMS is a robust cloud-based Software as a Service (SaaS) platform for managing clinical trials. Its unique architecture based on a modular system makes it 100% customizable. This ensures you can select the modules you need and remove the ones you do not in order to optimize your workflows, speed up procedures and space unnecessary expenses.

Phoenix CTMS est une application web moderne regroupant les fonctionnalités d'un logiciel de base de données en recherche clinique dans un système modulaire : PRS (Système de recrutement des patients), CTMS (Système de gestion des essais cliniques), CDMS (Système de gestion des données cliniques). Cet ensemble de fonctionnalités inégalées est conçu pour prendre en charge toutes les exigences opérationnelles et réglementaires du front-end clinique dans la recherche universitaire, les organismes de recherche sous contrat (CRO) et les hôpitaux menant des études cliniques, quelle que soit leur phase.

Contrôlez et gérez les essais cliniques et menez à bien les programmes de recherche clinique, tout en assurant le respect des contraintes réglementaires et des recommandations de la FDA. Ennov CTMS offre à la fois la surveillance des essais cliniques et la supervision multiétude. La visibilité et l'aide à la décision vous rendent plus efficace.

QMENTA Reader handles and streamlines the medical imaging workflow in clinical trials, ensuring quality and success all over the trial: - Create your personalized imaging workflow with our experts - Upload, anonymize and classify large amounts of data from multiple sites within seconds - Use AI & data to accurately select patients based on imaging endpoints - Create collaboration teams located in multiple spaces - Ensure quality of data and analysis anytime in the workflow with automated QC

eTMF Connect helps life sciences companies better manage their clinical trial documentation. Designed using the TMF Reference Model, eTMF Connect centralizes and standardizes your essential documents, enabling sponsors and CROs to contribute and access important clinical records and information in real-time. The solution's clinical eTMF functionality, advanced collaboration features including inspector view, and scalability, create a dynamic, intuitive, and powerful experience for users.

eClinPro is the most affordable integrated multi-functional system for all sizes of Clinical Research Sites. CTMS/ eSource/ eDocs/ Text SMS/ Recruitment Automation/ Integrated Calendar and many more powerful tools providing the perfect solution for Clinical Research Sites. The system was designed by CRCs, CRAs, Managers, PIs, facilitating the entire process since the recruitment starts to the closeout.

Data management software for clinical trials that is based on GCP and regulatory compliance, user friendliness, and affordability.

Cloud-based platform that enables clinical research professionals to manage study data, prepare reports and design workflows.

Study management for post-approval research and registries conducted by bio pharmaceutical companies, and research organizations.

Cloud-based solution that allows life science companies to manage clinical trial process providing clinical trial activities planning, tracking and control.

Comprehensive SAS based clinical data management, EDC, and clinical trials reporting system

Entrypoint is a complete web-based system for creating, deploying, and administering custom data entry applications, providing data entry access anywhere you are. Entrypoint architecture relies on a modular plug-in framework for maximum flexibility. The product consists of a web application for data entry and administration and three Desktop applications: Application Studio, Desktop Workstation and Desktop System Manager. All desktop applications communicate with the server.

A web-based data management solution that can be used for recruiting patients and managing all aspects of data associated with clinical research.

A comprehensive clinical research management information system.

Electronic pen and paper technology for clinical research / CRO.

Bring order to the complex world of human studies. Phase out disjointed legacy applications and paper-based processes and replace them with a single, browser-based application that facilitates collaboration between the research personnel that support the various aspects of a trial. Features include online trial design tool, eCRF builder, participant management, robust trial financials, automated event based billing, and a single point of reference for industry and investigator-initiated trials.

Dedicated to provide leading edge solutions and equipment purpose designed for clinical trial materials packaging.

TrialPoint modules are intuitive, flexible and powerful tools to manage all aspects of clinical trial lifecycle

Clindex is a state of the art product that offers integrated clinical data management, trial management and EDC functions in a single easy to use package. Offered both as web hosted or self-hosted Clindex is one of the most flexible and complete clinical solutions on the market!

Multi-channel acquisition software with programmable experiment control and automation with lock-In amplifier and photometry extension.

Clinical Research Organization with extensive experience in conducting Clinical Trials.

Les produits d'évaluation cognitive et de neurotechnologie accélèrent le développement clinique de la validation du concept au post-marketing. Ces outils se placent parmi les principaux en matière de tests cognitifs tactiles validés pour les essais cliniques de développement de médicaments qui sont sûrs et efficaces dans le cerveau humain.

Octalsoft Clinical Trails Management System provides a single, centralized system to manage sponsor and CRO study management activities.

Comprehensive and secure randomization software for clinical trials run entirely on the Internet. Features include accrual reports, verification of entry criteria, multiple treatment arms, stratification. random block sizes. email confirmations, optional collection subject data

Regulatory Management System that manages and monitors the regulatory side of a clinical trial.

Clinical data management solution with data queries generation, audit trails, electronic signatures, and data reconciliation tools.

SyMetric C6 - IWRS is unique in addressing the most diverse and demanding customer scenarios and web experiences, regardless of complexity, scale and duration of a study. With SyMetric C6 - IWRS you no longer have to worry about paying for expensive infrastructure. All our products and services are hosted on our virtual servers and are made available 24x7. Fully validated, 21 CFR Part 11 compliant System that allows you to automate many aspects of the trials with added flexibility.

Set of modules that help all stakeholders effectively manage all areas of clinical and research management.

i-CDMS est un système innovant basé sur le cloud offrant un ensemble complet de fonctionnalités permettant de simplifier la surveillance des essais et la saisie de données avec e-CRF, la résolution automatisée des vérifications de montage et des requêtes, le reporting sur les patients et les sites, les notifications et rappels en temps réel, etc. tous les participants à l'essai en fonction de leurs rôles. i-CDMS a été construit avec les outils technologiques les plus récents et une interface utilisateur ultramoderne consistant en un CDE entièrement qualifié pour la prise en charge des essais cliniques.

Cronos provides end-to-end e-clinical solutions, for clinical trials, BA-BE studies, Screening and volunteer management. It has complete solution starting from subject registration till report compilation. Cronos is fully compliant to the guidelines of 21 CFR part 11 and other regulatory authorities. Customization is possible in the system as per the organization's requirements. All the modules of the system can run as a standalone and can also run on a integrated platform.

MasterControl Inc. développe des solutions logicielles qui permettent aux entreprises réglementées de commercialiser leurs produits plus rapidement, tout en réduisant les coûts globaux et en augmentant l'efficacité interne. MasterControl gère en toute sécurité les informations stratégiques sur l'ensemble du cycle de vie des produits. Découvrez pourquoi plus de 1 000 entreprises ont choisi MasterControl pour automatiser leurs mesures préventives et correctives, le contrôle des documents, le contrôle des modifications, la formation, la gestion des audits et d'autres processus réglementaires et de gestion de la qualité.

Solution Cloud pour les leaders des essais cliniques. Les fonctionnalités comprennent l'inscription numérique, l'engagement des participants et le reporting.

Electronic Data Capture (EDC) solution streamlines the initiation and management of clinical trials.

Unified clinical trial management solution built on Salesforce.com platform with end-to-end capabilities covering planning, start-up, conduct, and close out. Capabilities include: Account Management, Site Performance Metrics, Feasibility Reports, Start-up & Study Management, Project & Milestone Management, Budget Management, Site Management,Essential,Document Checklist, Subject Management, Adverse Events, Protocol Deviation, eCRF, Payments & Invoices, Virtual Trial, Patient Recruitment