Logiciels de gestion d'essais cliniques

IBM Clinical Development from Watson Health is a global SaaS solution that can help the life-sciences transform clinical research and may accelerate the delivery of needed therapies to patients. With a powerful electronic data capture (EDC) system at its core, IBM Clinical Development affords clinical researchers access to hidden insights and visibility into their trial data. Scalable in both feature and function, we offer a robust suite capabilities that can be tailored to all clinical trials. En savoir plus sur IBM Clinical Development

Un système de saisie électronique des données pour les essais cliniques adapté aux mobiles. Conçu par des chercheurs, pour des chercheurs. Les fonctionnalités comprennent la création d'eCFR en libre-service (création de formulaires), la distribution aléatoire, l'ePro (enquêtes auprès des patients), le monitoring, l'importation et l'exportation faciles de données, l'importation de données du dossier médical partagé (basé sur HL7 FHIR), les pistes de vérification, la gestion des utilisateurs et bien d'autres choses encore. Le système est entièrement certifié ISO 27001, BPC et 21 CFR et il a des serveurs aux États-Unis (conformes HIPAA), au Royaume-Uni, aux Pays-Bas et en Allemagne. Les petites études sont gratuites dans Castor EDC ! En savoir plus sur Castor EDC

Clinical Conductor est un système de gestion des essais cliniques (CTMS) conçu pour les sites de recherche, les hôpitaux, les AMC, les réseaux de sites, les systèmes de santé et les CRO. Il aide les organisations menant des recherches cliniques à être plus efficaces et rentables. Le CTMS Clinical Conductor est l'application leader sur le marché, il facilite les procédures d'essai clinique et permet aux organisations de prendre de meilleures décisions commerciales et de relever tous les défis. En savoir plus sur Clinical Conductor CTMS

Les protocoles sont complexes. Obtenir des données ne devrait pas l'être. Avec un concepteur d'études collaboratif par glisser-déposer et des formulaires mobiles pour vos sites et vos sujets, OpenClinica fait bien plus que recueillir des données. Il offre une meilleure expérience. Résultat ? Des données de meilleure qualité pour vos études, à un coût réduit, ce qui facilite également la budgétisation. Chaque déploiement comprend un hébergement cloud sécurisé et performant sur AWS, une validation documentée, et la conformité FDA, EMA, GDPR et HIPAA En savoir plus sur OpenClinica

Medrio fournit des solutions de saisie électronique des données (EDC) efficaces et faciles à utiliser, y compris une gamme de produits équipés de sources électroniques, pour les essais cliniques. Ce logiciel est entièrement hébergé dans le cloud, ne nécessite aucune programmation et coûte 75% de moins que les solutions EDC traditionnelles. Depuis sa création, certaines des plus grosses sociétés pharmaceutiques, de dispositifs médicaux et de CRO du secteur ont utilisé ce système conforme à la norme 21 CFR Part 11 pour réduire de façon drastique leur temps d'élaboration. En savoir plus sur Medrio

Plateforme de prise en charge des études clinique, Longboats crée un environnement dans lequel la conformité aux protocoles est instinctive, les équipes bénéficient d'une aide virtuelle dès qu'elles en ont besoin et tous les intervenants disposent des connaissances et des ressources nécessaires à la bonne marche de l'étude. Les responsables des activités cliniques et de la surveillance, le personnel sur site et les patients ont tous accès à cette plateforme intégrée et cohérente de prise en charge. L'interface et le niveau de prise en charge changent en fonction des besoins spécifiques de chaque utilisateur prenant part à l'étude. En savoir plus sur Longboat

Ethical eAdjudication est un service logiciel cloud GxP d'évaluation des critères cliniques conçu pour accompagner les directeurs de recherches, les membres de comités et les professionnels affectés au contrôle de la qualité dans l'examen central et l'évaluation de critères subjectifs. Il fournit les outils et services indispensables pour mener une procédure indépendante de révision et d'évaluation opportune et efficace dans le respect des normes de qualité. En savoir plus sur eAdjudication

RealTime-CTMS is the leading clinical trial management system designed to increase efficiency and profitability for research sites and site networks. With fully-integrated services such as RealTime-TEXT, RealTime-PAY and the first fully-integrated eRegulatory document management system, RealTime-eDOCS, RealTime Software Solutions, LLC has the complete package of tools to help sites excel. No other CTMS can do all that RealTime does! En savoir plus sur RealTime-CTMS

ClinPlus CTMS & eTMF is the core clinical trial data tracking of the ClinPlus suite offering EDC, IWRS in a unified platform, utilizing a single sign-in and a role-based tailored user interface for all functionality. ClinPlus CTMS provides end to end study start up to close out monitoring visit reports, easy navigation for quick, affordable seamless unification to avoid integration costs, and document management for all types of clinical trials delivered in 6 weeks via a secure, private cloud. En savoir plus sur Clinical Trials Management

Clinical Studio est un produit SaaS entièrement basé sur le cloud. Il contient des logiciels spécialement conçus pour révolutionner la recherche clinique, ce qui permet aux entreprises de mener à bien leurs essais de manière efficace à l'aide d'un système conforme à la norme 21 CFR Part 11. Clinical Studio redéfinit les logiciels de recherche clinique en s'appuyant sur des logiciels intégrés et des applications mobiles natives afin de simplifier la conception, le déploiement et la gestion des études cliniques. En savoir plus sur Clinical Studio

Système de saisie électronique des données (EDC) et de gestion des données, flexible et convivial, pour les essais cliniques, la recherche épidémiologique, la randomisation du web (IWRS), les registres des patients, les EPRO (rapports électroniques de patient) et les sondages sur le web. Ce logiciel fournit l'interface la plus facile à utiliser et intuitive sur le marché avec des dispositifs et des options de conception non disponibles dans d'autres produits de logiciel. En savoir plus sur Dacima Clinical Suite

Ripple is a web-based recruitment-focused patient and study management tool for clinical and translational studies. Ripple provides clinical sites with a centralized software to manage all aspects of recruitment and post-enrollment tracking of patients in clinical trials. Ripple helps clinical trial sites enroll more patients, increase retention, simplify reporting, and automate tasks in order to provide an excellent, patient-centered experience to trial participants. En savoir plus sur Ripple

Story by PulsePoint makes content marketing more efficient, more effective and more trackable. We extend your targeted reach across premium social, native, and content discovery channels. Our platform optimizes to your KPIs to maximize engagement and deliver clear ROI. How it works: Upload your content via URL and create multiple headline/image variants for each channel seamlessly, choose your channels you want to advertise on. Story optimizes towards KPIs. En savoir plus sur Story

The Pristima® Suite is a fully integrated, preclinical software platform that delivers full life cycle automation for drug discovery

Pour des projets de recherche clinique : gestion de projet, évaluation de faisabilité, inscription, saisie de données, compilation, archivage.

Self-configurable workflow management tool for clinical trials. Functionality includes patient recruitment and remote monitoring.

Les produits d'évaluation cognitive et de neurotechnologie accélèrent le développement clinique.

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

Un système complet de gestion des données cliniques pour la collecte des données d'essai clinique.

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

A great tool that assists organizations to collect Trial specific data to track study performance, schedule, monitor, and more.

OnCore® Enterprise Research is a comprehensive clinical research management system.

Redefine clinical trial regulatory document and TMF management with an automated, customizable 21 CFR Part 11 compliant solution.

Integrates comprehensive functionalities needed in the clinical trials process into a single, open web platform.

Assurez-vous que les échantillons de laboratoire sont collectés, manipulés et traités avec précision grâce à la solution STARLIMS Clinical Research.

MAISi est un système de gestion d'essais cliniques convivial et sophistiqué qui a été conçu pour aider les sites de recherche clinique.

A comprehensive clinical research management information system.

DataFax is a mature and stable Clinical Trial System, that is a true hybrid system.

Comprehensive system that allows to securely keep specimen data from multiple studies and supports various data mining tools.

Clinicians can view live clinical trial patient data in real-time, in a colorful, graphical presentation on their own desktop computer.

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

Web and telephone-enabled electronic data capture of patient reported outcomes.

Web based SaaS EDC solution for clinical trial management. Features include compliance, data export, and medical coding.

A clinical trial management solution connecting protocol, study training, videos, study contact, visit schedule, and more.

The leading Clinical Trial Knowledge Platform, offering a transformative collaboration channel and clinical trial oversight.

Streamlines paper-based clinical data entry, and provides real-time data access and enhanced data quality.

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

Collecte électronique de données pour tous les essais, de la phase I à IV, pouvant évoluer d'un site unique à de grands essais internationaux.

Enables clinical research professionals to collect and manage study data nearly twice as fast as the industry average.

Snappii offers 400+ live business apps in 30 industries for every business. Get the mobile app for your business in days, not months.

Clinical Research Organization with extensive experience in conducting Clinical Trials.

21 CFR Part 11 Compliant, Web-Enabled eClinical Suite with integrated Clinical Trial Management.

Broad, flexible and modular CTMS solution delivered to small to mid sized sponsors or CROs.

Clinion is a user friendly 21 CFR Part 11 validated Intuitive EDC and CDM software.

Cloud based platform with unified apps to optimize workflow processes, site engagement and training for global clinical trials.

Online Clinical Trial Management System for handling and administration of all tasks (operational and logistical).

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

Protect important information with extensive security, manage data and analyze documents to create reports

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

Coordinates complex trial processes and manages enterprise-level data.

Allegro CTMS is a cloud-based clinical trial management system that manages the operational data of small to mid-sized research sites.

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

Allows for the collection and management of a wide variety of different types of data for applied behavior analysts.

For automating environmental, public health, clinical/toxicology, utility, process control and related laboratories.

Intuitive web-based platforms and on-line database applications for the design and management of clinical trials and registries.

CTMS used to create a natural next step to bring Office tools, business process workflow, and documents into the regulated world.

A complete system for creating, deploying, and administering custom data entry applications .

BSI CTMS covers all aspects of clinical trial management. It is the most intuitive and flexible system on the market. Test us out.

Pedigree, family history and risk assessment software used by genetic counselors, clinicians and researchers.

Solution for research sites, universities, and hospitals streamlines clinical research, providing real-time access to key metrics.

A software-based environment for running large-scale, time-critical applications on commodity-grade computers.

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

Comprehensive software solutions for research administration and compliance.

A solution that enables bio-pharma and clinical research organisations to capture critical patient related details for clinical trials.

CTM on Salesforce 1 cloud platform for sponsors, clinical research organizations (CRO), hospitals and medical centers.

Unified eClinical technology (EDC/DM plus 15 integrated modules plus reporting) for small-to-mid size life sciences companies.

QlikView puts information at your fingertips and frees you to make quick decisions, giving you intelligence you need to act faster.

Software to help manage all tasks and documentation within clinical trials.

Flex Databases is a company providing e-solutions for clinical trials.

Web based LIS platform enabling automated sequencing genotyping in a molecular diagnostic, clinical research environment.

An innovative, next-generation EDC/eClinical solution that allows non-technical research personnel to easily build their own studies.

Enable researchers to collect, interpret and distribute cardiac safety and clinical data accurately and efficiently.

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

Helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development.

Cloud-based solution with clinical trial activities planning, tracking and control for life science organizations.

DSGs award-winning eCaseLink software is the most advanced Electronic Data Capture (EDC) solution in the industry.

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

Electronic pen and paper technology for clinical research / CRO.

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

SimpleTrials is a Clinical Trial Management System for Sponsors, CROs and Sites. Plans start at $35/month with no long term commitment

Solution designed to help life sciences organizations manage all aspects of clinical trials efficiently and effectively.

Clinical trail management system that provides a single, centralized system to manage sponsor and CRO study management activities.

Create the patient's clinical story and assign appropriate clinical terminology through computer-assisted coding.

Software that provides document routing, submission tracking, protocol deviation review, and strict data access control,

Fully-integrated, web-based solution 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.

Cloud based EDC system with online safety, compliance monitor, real time analyses.

The DATATRAK ONE Unified Experience removes complexities, activating better site compliance, better data, and safer trials.

Cronos has a complete solution for a clinical research organization conducting clinical trials and EDC solution for BA-BE studies.

A comprehensive end-to-end clinical trials management solution for pharmaceutical and life sciences organizations.

Secure, web based CTMS for research teams who want to easily interact with patients. Features include onboarding and study management.

Blue Skys Path Clinical Training Portal is a powerful tool to support the training of clinical site personnel.

Help your Clinical Operations team continuously improve speed, efficiency and data quality across your portfolio of clinical trials

A disruptive big data SaaS platform, that accelerates new drug launches,lowers clinical trial costs, and enables RBM.

Cloud based computer system for entering, storing, extracting, analysing and reporting of Clinical Trials Data.

A powerful Clinical Management System with end to end modules such as appointment scheduling, billing, EMR, and more.

Trials.ai leverages artificial intelligence to manage clinical trials.

Are you tired of using a CTMS that is overcomplicated, has a poor interface and costs too much? Contact us to learn more.

Data+ was designed by researchers and for researchers. We focus on Simplicity, Database Enrichment and Patient Engagement.

An interactive environment for multimodal biosignal data processing and analysis in the fields of clinical research and life sciences

Document management system designed for handing documents dealing with clinical trials management.

An electronic source data, lab routing and CTMS system built for clinical research sites.

As "Champions of the Paperless Clinical Trial", the Target Health eSource EDC software suite facilitates clinical trials of all sizes!

ClinicSoftware.com provides 360-degree view of your customers to help you build a strong relationship with your customers and grow!

Clinical Assay Management provides a consistent approach to the collection & management of clinical research study data.

Easy to custom and to use, fully integrated with IVRS and DSM.

Centralized software which provides ways to manage, track, and document throughout the clinical trials process.

Offers integrated clinical data management, trial management and EDC functions in a single easy to use package.

An easy-to-use affordable clinical trial data mangement system specifically designed for clinical research sites.

Comprehensive and secure randomization software for clinical trials run entirely on the Internet.

Address diverse and demanding customer scenarios and web experiences, regardless of complexity, scale, and duration of a study.

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

Investigator's first choise EDC - eCRF for all types of clinical trials

Data MATRIX is a company providing full-service data management services based on the in-house developed EDC/IWRS software.

Provides integrated solutions to automate Electronic Data Capture, Data Management, and Project Management needs.

KLINDAT is a next-generation electronic Case Report Form (eCRF) for the pharmaceutical, biotech & medical device industries.

A new breed of cloud-based, patient-centric data capture solutions designed to handle both ePRO and EDC on BYOD.

An advanced clinical trial management system (CTMS) allowing multiple studies across different sites to be supported.

A cloud base software solution developed to speed the startup of clinical trials to impact patient enrollment.

Practice management software that is highly configurable for any customer requirements.

Comprehensive eSource system for all the source data for clinical trials with source, regulation, and drug accountability.

Ready to use clinical trials management platform that helps govern all parts of the research process.

Configurable CTMS that helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases.

Powerful open source (LGPL) CTMS/CDMS/subject registry database system, created at Medical University of Graz.

HealthStream Competency Center is competency-driven, healthcare specific, and a HealthStream-integrated competency management system.