Electronic data capture platform that provides the recording of patient-reported outcome data through a centralized database.

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.

IBM Clinical Development von Watson HealthTM ist eine Cloud-basierte Datenmanagement-Lösung, dank der klinische Forscher Studien mit Genauigkeit, Komfort und Vertrauen erstellen und verwalten können. Es hebt ein leistungsstarkes Datenerfassungssystem hervor und bietet End-to-End-Klarheit der Studiendaten, so dass Anwender Erkenntnisse gewinnen, die mit anderen modularen Systemen nicht möglich sind. Innerhalb seiner dynamischen Struktur ist die Grundlage für neue Entwicklungen patientenzentrierte Ansätze und Watson kognitive Technologie.

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 bindet die Erfassung von klinischen Daten (z.B. Patientenberichte (PROMs/PREMs) und Prüfbögen (CRFs)) und die KI-unterstützte Analyse medizinischer Bilder (CT, MRT, Röntgen) in den klinischen Alltag ein und automatisiert Routineaufgaben des Studienmanagements, der Datenerhebung und -analyse. UNITY wurde mit dem Ziel entwickelt, Krankheiten zu erfassen und früher zu erkennen, Komplikationsraten zu senken und die Versorgung von Patienten insgesamt zu verbessern.

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

A comprehensive clinical research management system, OnCore® Enterprise Research supports centralized operations at academic medical centers, cancer centers, and health care systems. The OnCore system includes clinical research management, billing compliance, electronic data capture, biospecimen management, patient registries, and integrations for the research enterprise.

Einfach zuzuschneiden und zu verwenden, vollständig mit IVRS und DSM integriert.

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.

Für Organisationen, die an klinischen Studien teilnehmen, bietet die Verwaltungssoftware BioClinica CTMS für klinische Studien einen natürlichen nächsten Schritt, um Office-Tools, Geschäftsprozess-Workflow und Dokumente zu regulieren.

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.

Klinisches Datenmanagementsystem mit optimiertem Ansatz zur Erstellung von Studien und detaillierter Berichterstattung.

MAISi von Agile Health Computing ist ein benutzerfreundliches und ausgeklügeltes Managementsystem für klinische Studien, das dem Verwaltungsbedarf klinischer Forschungseinrichtungen gerecht wird. Durch die Erfassung und Überwachung geschäftlicher Kennzahlen an den Ausführungsorten klinischer Studien erleichtert MAISi die Implementierung von Protokollen und sorgt für ein verbessertes Zeit- und Finanzmanagement, was in diesem hart umkämpften internationalen Markt eine wichtige Rolle spielt.

MedSciNet is a Stockholm based company specialising in design and development of web applications and on-line database systems for clinical trials and studies, quality registries, medical bio-banks, and other solutions within the medical field. MedSciNet has offices in London (UK), Vilnius (Lithuania), Stockholm (Sweden) and Cork (Ireland).

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 ist eine leistungsstarke, webbasierte Softwarelösung für klinische Studien. Die vollständige Einhaltung der GCP- und FDA 21 CFR Part 11-Vorschriften wird gewährleistet und gleichzeitig werden höchste Qualitätsstandards garantiert. secuTrial bietet ein hohes Maß an konzeptioneller Freiheit in Bezug auf Studiendesign, Flexibilität und Benutzerfreundlichkeit. Es kann daher auf vielfältige Weise für alle Phasen klinischer Studien verwendet werden, beispielsweise für klinische Studien zur Zulassung oder für Phase-IV-Studien.

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 ist eine moderne Webanwendung, die die Funktionen von Datenbanksoftware kombiniert, die in der klinischen Forschung in einem modularen System verwendet werden: PRS (Patientenrekrutierungssystem), CTMS (Clinical Trial Management System) und CDMS (Clinical Data Management System). Dieses unübertroffene Funktionsset unterstützt alle operativen und regulatorischen Anforderungen des klinischen Frontends in der akademischen Forschung in CROs (Contract Research Organizations) und Krankenhäusern, die klinische Studien aller Phasen durchführen.

Das Ziel des CTMS besteht darin, bei der Überwachung und Verwaltung zahlreicher klinischer Studien effizienter zu sein, die notwendig sind, um klinische Forschungsprogramme zu einem erfolgreichen Abschluss zu bringen und gleichzeitig die Einhaltung der regulatorischen Auflagen und Empfehlungen der FDA sicherzustellen. Ennov CTMS bietet sowohl die Überwachung von klinischen Studien als auch die Überwachung mehrerer Studien an. Sichtbarkeit und Entscheidungshilfen helfen dir, effektiver zu werden.

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.

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.

Ein umfassendes Managementinformationssystem für die klinische Forschung.

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!

Mehrkanal-Akquisitionssoftware mit programmierbarer Experimentiersteuerung und -automatisierung mit Lock-In-Verstärker und Photometrie-Erweiterung.

Unternehmen für die klinische Forschung mit umfangreicher Erfahrung in der Durchführung von klinischen Studien.

Kognitive Assessment- und Neurotechnologie-Produkte beschleunigen die klinische Entwicklung vom Proof of Concept bis zum Post-Marketing. Führende Anbieter von validierten kognitiven Touchscreens für klinische Studien zur Entwicklung von Arzneimitteln, die im menschlichen Gehirn sicher und wirksam sind.

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 is an innovative cloud based system offering a complete set of features for streamlining trial monitoring and data entry with e-CRF, automated edit checks and queries resolution, patient and site reporting, real time notifications and reminders and others that are accessible from all trial participants according to their roles. i-CDMS has been built with the latest technology tools and state of art user interface consisting a fully qualified EDC for supporting clinical trials

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. entwickelt Softwarelösungen, die es regulierten Unternehmen ermöglichen, ihre Produkte schneller auf den Markt zu bringen, während gleichzeitig die Gesamtkosten gesenkt und die interne Effizienz gesteigert wird. MasterControl verwaltet die kritischen Informationen eines Unternehmens sicher über den gesamten Produktlebenszyklus. Erfahre, warum sich mehr als 1.000 Unternehmen für MasterControl entschieden haben, um ihre CAPA-, Dokumentenkontroll-, Änderungskontroll-, Schulungs-, Auditmanagement- und andere Qualitätsmanagement- und Regulierungsprozesse zu automatisieren.

Cloud based solution for clinical trial leaders. Features include digital enrollment, engagement of participants, and reporting.

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