Clinical Trial Software
Clinical Trial Software hilft bei der Verwaltung aller Aspekte von klinischen Studien, einschließlich Patientendaten, Terminplanung, Berichterstattung, Analyse und Datenmanagement. Diese Art von Software kann auch Tools zur Patientenregistrierung, Studienplanung, Rekrutierung und Entscheidungsfindung in Reaktion auf Patientendaten bereitstellen. Clinical Trial Software ist mit Software für die Verwaltung von Gesundheitseinrichtungen und Medizinische Laborsoftware eng verbunden.
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- Cloud, SaaS, Web (94)
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- 21 CFR Part 11-Compliance (81)
- Dokumentenmanagement (71)
- Elektronische Datenerfassung (64)
- HIPAA konform (63)
- Patientendatenbank (62)
- Personalbeschaffung-Management (42)
- Registrierungs-Management (60)
- Studienplanung (63)
- Terminplanung (60)
- Überwachung (75)
At ClinCapture our mission is to build software that saves lives. Our technology lowers the cost of clinical trials by streamlining data capture processes while providing a platform that protects patient privacy. ClinCapture advances the evaluation and development of drugs, biologics, and devices that demonstrate promise for the diagnosis and/or treatment of a wide range of diseases or medical conditions. Request a demo today! Erfahre mehr über ClinCapture ClinCapture provides all of its customers with Private Cloud EDC, so your privacy is always protected. Request a demo today! Erfahre mehr über ClinCapture
Clinical Conductor CTMS ist das klinische Trial Management System (CTMS), für Forschungseinrichtungen, Krankenhäuser, AMCs, Objektnetze, Gesundheitssysteme und CROs. Clinical Conductor ermöglicht es Unternehmen, die klinische Forschung der Durchführung effizienter und profitabler zu gestalten. Clinical Conductor CTMS ist die marktführende Anwendung, die Testprozesse einfacher macht und es Unternehmen ermöglicht, bessere Geschäftsentscheidungen zu treffen und für jede Herausforderung bereit zu sein. Erfahre mehr über Clinical Conductor CTMS Clinical Conductor ist das führende CTMS für Forschungsstandorte, Standortvernetzungen, Krankenhäuser, AMCs, CROs und Gesundheitssysteme. Erfahre mehr über Clinical Conductor CTMS
Medrio bietet klinischen Forschern eine effiziente und nutzerfreundliche elektronische Datenerfassungslösung (EDC) sowie eine Suite nativer Tablet-Apps für eSource und ePRO. Die Software wird vollständig in der Cloud gehostet, erfordert keine Programmierung für Studienerstellungen oder Änderungen während der Studie und ermöglicht Sponsoren und CROs von klinischen Studien aller Art, ihre Studienkosten zu senken. Hunderte von Organisationen aus den Bereichen Pharma, Medizinprodukte, Diagnostik und Tiergesundheit haben die Software seit der Gründung eingesetzt. Erfahre mehr über Medrio Medrio bietet schnelle und nutzerfreundliche eClinical-Lösungen ohne Programmieraufwand. Erfahre mehr über Medrio
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. Erfahre mehr über Ripple Ripple facilitates the recruitment and management of patients for clinical and translational studies. Erfahre mehr über Ripple
Ein mobile-freundliches, elektronisches Datenerfassungssystem für klinische Studien, von Forschern für Forscher gebaut. Zur Ausstattung gehören Self-Service ECFR Kreation (Formular-Erstellung), Randomisierung, ePro (Patientenbefragungen), Überwachung, einfacher Import und Export von Daten, EHR Datenimporteur (HL7 Fhir basiert), Audit-Trails, Benutzerverwaltung und vieles mehr. Wir sind vollständig ISO 27001 zertifiziert, GCP und 21 CFR konform und bieten Server in US (HIPAA), UK, NL, DE Kleine Studien sind kostenlos bei Castor EDC! Erfahre mehr über Castor EDC Der einzige GCP & 21 CFR konformes System, das für jeden Forscher erschwinglich ist und über alle Funktionen von teueren Systemen verfügt. Jetzt starten. Erfahre mehr über Castor EDC
Protokolle sind komplex. Das Erhalten von Daten sollte es nicht sein. Mit einem kollaborativen, Drag-and-Drop-Studio-Designer für dich und schönen, mobil-freundlichen Formularen für deine Websites und Themen ist OpenClinica mehr als nur Datenerfassung. Es ist eine bessere Erfahrung. Das Ergebnis? Qualitativ hochwertigere Daten für deine Studie, zu Kosten, die ebenfalls die Budgetierung einfach machen. Erfahre mehr über OpenClinica Studiendesign, EDC, ePRO, IxRS und gehaltreiche Datenvisualisierungen - alles auf einer benutzerfreundlichen Plattform. Hier sind Deine klinischen Daten, verwaltet. Erfahre mehr über OpenClinica
Die Support-Plattform für klinische Studien mit Longboats schafft ein Umfeld, in dem die Einhaltung von Protokollen instinktiv ist, Teams zu jeder Zeit virtuell geführt werden und alle Beteiligten über das Wissen und die Ressourcen verfügen, die sie für die Durchführung der Studie benötigen. Klinische Operationen, Überwacher, Mitarbeiter vor Ort und Patienten greifen auf die eine integrierte und konsistente Support-Plattform zu. Abhängig von der Rolle des Benutzers in der Studie werden die Schnittstelle und die Unterstützung angepasst, um deine spezifischen Anforderungen zu erfüllen. Erfahre mehr über Longboat Eine Managementlösung für klinische Studien mit einer Leistung und Beteiligten-Dashboard, Patientenkalender und Memos und mehr. Erfahre mehr über Longboat
Ethische eAdjudication für klinische Endpunkt Jurierung ist ein GxP-Software-Service, basierend auf einer Cloud-Plattform, um Studienleiter, Ausschussmitglieder und QA-Mitarbeiter bei der zentralen Überprüfung und Beurteilung subjektiver Endpunkte zu unterstützen. Es bietet die richtigen Werkzeuge / Dienstleistungen, um die unabhängigen Untersuchungs- & Jurierungsverfahren in angemessene, wirksame und auf Qualität kontrolliere Art und Weise zu erreichen. Erfahre mehr über eAdjudication Endpoint Adjudication Cloud-Software-Service. Ausgelegt für GxP Compliance & Effektivität Erfahre mehr über 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! Erfahre mehr über RealTime-CTMS Research sites & networks looking to streamline study information and company processes. We guide customers from study start to finish. Erfahre mehr über 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. Erfahre mehr über Clinical Trials Management ClinPlus CTMS - Designed specifically to help organizations overcome the technical challenges associated with managing clinical trials. Erfahre mehr über Clinical Trials Management
Clinical Studio ist ein echtes Cloud-basiertes SaaS (Software-as-a-Service) -Produkt, das aus speziell gebauter Software besteht, die klinische Forschung verwandelt, damit Unternehmen effizient komplette Studien auf einem 21 CFR Part 11-kompatiblen System durchführen können. Clinical Studio definiert klinische Forschungs-Software neu, durch den Einsatz von integrierter Software und nativen mobilen Anwendungen, um Design, Bereitstellung und Verwaltung von klinischen Studien zu optimieren. Erfahre mehr über Clinical Studio Clinical Studio erleichtert die Forschung indem es für eine Pauschalgebühr auf Anfrage Enterprise IT-Infrastruktur liefert. Erfahre mehr über Clinical Studio
Flexible, user-friendly, web-based electronic data capture (EDC) and data management system for clinical trials, epidemiological research, web randomization (IWRS), patient registries, ePRO and web surveys. Our software provides the most easy to use and intuitive interface on the market with features and design options not available in other software products. Erfahre mehr über Dacima Clinical Suite Flexible, user-friendly, web-based electronic data capture (EDC) and data management system for clinical trials and research. Erfahre mehr über Dacima Clinical Suite
Intellect offers the industry's most configurable enterprise Quality Management Software (eQMS) suite and platform. Lower your total cost of ownership, reduce product recalls, and improve operations by easily modifying your applications to meet your exact requirements using Intellect's no-code platform. Learn how you can effectively and efficiently manage your Nonconformance, CAPA, Document Control, Change Management, Audit, Training, Risk Management and many other QMS and business processes. Erfahre mehr über Intellect Intellect eQMS is hyper-adaptive quality management solution that meets your unique needs and lowers your total cost of ownership. Erfahre mehr über Intellect
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. Erfahre mehr über Story Manage, distribute and optimize your content across premium publishers through 25+ social, native and content discovery partners. Erfahre mehr über Story
Pristima ist für das präklinische Datenmanagement eine vollständig integrierte Unternehmenslösung, die eine komplette Lebenszyklus-Automatisierung und Unterstützung für die Pharmakologie und das Studienmanagement von Arzneimittelsicherheitsforschung, Vivarium-Management und tierärztliche Betreuung liefert. Von der Zucht über den Prozess der Forschungsvorlage bis hin zur Bestellung verwaltet die Pristima Suite die Planung und Erfassung von Daten, kontrolliert zugelassene Änderungen und sammelt die Daten zur Vorlage bei den Regulierungsbehörden. Die Pristima® Suite ist eine vollständig integrierte, präklinische Software-Plattform, die eine komplette Lebenszyklus-Automatisierung für die Entdeckung von Arzneimitteln bereitstellt.
BizNET, A clinical trials management software offers an integrated suite of software products for CROs, Pharmaceutical, Biotech Industries and Medical device industries. Our solution blends various integrated modules that prominently support clinical trial activities like EDC/DDC data collection, IWRS & drug randomization management, CDISC SDTM. It is a validated software, compliant with 21 CFR part 11 and GCP guidelines which provide a transparent and smooth process to regulatory For clinical research projects - project management, feasibility assessment, enrollment, data capture, compilation, archiving.
Self-configurable workflow management tool for clinical trials. Functionality includes patient recruitment and remote monitoring. Self-configurable workflow management tool for clinical trials. Functionality includes patient recruitment and remote monitoring.
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. Kognitive Beurteilung und neurotechnologische Produkte beschleunigen die klinische Entwicklung.
Cloud based solution for clinical trial leaders. Features include digital enrollment, engagement of participants, and reporting. Cloud based solution for clinical trial leaders. Features include digital enrollment, engagement of participants, and reporting.
Delve is a cloud based solution providing a search engine allowing users to look at data across multiple streams identifying what they need. The most popular use cases that our clients have used Delve for are: 1. Automating Literature Review. 2. Pre-qualify Investigators and Sites based on the work they have done in regards to Clinical Trials and publications conducted. 3. Gather insights in regards to the different trials conducted, where they happened and so forth. A great tool that assists organizations to collect Trial specific data to track study performance, schedule, monitor, 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. OnCore® Enterprise Research is a comprehensive clinical research management system.
Verwalte Dokumente, Signaturen und Fristen mit Leichtigkeit. Teile Dokumente überall und jederzeit sicher. RDMS bietet Dashboards für Test- und Dokumentenverwaltung, elektronische Signaturerfassung nach 21 CFR Part 11, dynamische Datenaktualisierungen, automatisches Ausfüllen von Formularen, Termintrigger und Änderungsverlauf. Flexible und skalierbare VACAVA-Lösungen werden über die Cloud bereitgestellt, sodass du dich nie um Technologiedetails kümmern musst. Definiere regulatorische Dokumente für klinische Studien und das TMF-Management neu mit einer automatisierten, anpassbaren Lösung nach 21 CFR Part 11.
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. MAISi ist ein benutzerfreundliches und ausgeklügeltes Verwaltungssystem für klinische Studien, das für klinische Forschungseinrichtungen entwickelt wurde.
Since 1992, DataFax has been in use by CROs, Pharmaceuticals/Medical Device companies, and Global Health Organizations for the past 23 years. DataFax is an EDC system with a hybrid approach that allows our user the flexibility of designing a study/trial by EDC, paper, or both. We provide a cloud/hosted solution or clients can host the database in-house. Users will have the option of selecting from a single study fee structure or a full license, which will allow 100 plus studies. 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. Comprehensive system that allows to securely keep specimen data from multiple studies and supports various data mining tools.
Patient Profiles is software that reads clinical trial datasets and creates individual reports (PDF, Word, HTML) for each patient. It provides both easy access to the most common tasks - reading data and creating standard profiles, for example, as well as the flexibility to adapt to the specifics of each trial and set of datasets - changing data types and formats, deriving new variables, and transposing long, skinny data structures. Perfect for clinical data managers. 30-day demo available. Clinicians can view live clinical trial patient data in real-time, in a colorful, graphical presentation on their own desktop computer.
A clinical trial management solution connecting protocol, study training, videos, study contact, visit schedule, and more. A clinical trial management solution connecting protocol, study training, videos, study contact, visit schedule, and more.
iDiary is ideal for a wide range studies from low to high complexity, providing sponsors with flexibility to capture patient information from early clinical development through commercialization (phase IV and health outcomes studies). 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. Web based SaaS EDC solution for clinical trial management. Features include compliance, data export, and medical coding.
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. The leading Clinical Trial Knowledge Platform, offering a transformative collaboration channel and clinical trial oversight.
Multi-channel acquisition software with programmable experiment control and automation with lock-In amplifier and photometry extension. Multi-channel acquisition software with programmable experiment control and automation with lock-In amplifier and photometry extension.
Elektronische Datensammlung für alle Studien, von Phase I bis IV, Skalierung von einem einzelnen Standort zu großen internationalen Studien. Elektronische Datensammlung für alle Studien, von Phase I bis IV, Skalierung von einem einzelnen Standort zu großen internationalen Studien.
Enables clinical research professionals to collect and manage study data nearly twice as fast as the industry average. Enables clinical research professionals to collect and manage study data nearly twice as fast as the industry average.
Snappii offers many mobile apps for the Pharma-Bio Industry as a convenient and easy-to-use mobile solution that will save time and avoid unnecessary procedure, make it easy to share pharmacy information among pharmacists, eliminate mistakes caused by human factor, enable rapid and accurate data collection. App users can upload their own PDFs, edit them and share. Choose from 400+ ready-made apps or we can create the app for you. Snappii offers 400+ live business apps in 30 industries for every business. Get the mobile app for your business in days, not months.
Robust, flexible, SaaS-based Clinical Trial Management Solution (CTMS) delivered to Sponsors or CROs. Functionality includes: * Project Management * Supplies * CRF and DCF Tracking * Sponsor and Investigator Portal * Clinical Payments * Timesheet & expenses * Monitoring reports * SAE tracking * Offline Client Broad, flexible and modular CTMS solution delivered to small to mid sized sponsors or CROs.
EasyTrial is an online Clinical Trial Management System for handling and administration of all tasks (operational and logistical) in clinical studies, so healthcare professionals can use their time efficiently. The system has been developed by Danish doctors experienced in conducting clinical trials. EasyTrial is compliant with Good Clinical Practice (GCP) and legislation applicable to database security and it provides maximum security, study overview and resource handling. 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. Study management for post-approval research and registries conducted by biopharmaceutical companies, and research organizations.
Schütze wichtige Informationen mit umfassender Sicherheit, verwalte Daten und analysiere Dokumente, um Berichte zu erstellen. Schütze wichtige Informationen mit umfassender Sicherheit, verwalte Daten und analysiere Dokumente, um Berichte zu erstellen.
Allegro CTMS is a cloud-based clinical trial management system that efficiently manages the operational data of clinical trials for dedicated research sites, physician practices, and community hospitals. Its superior usability, coupled with the right amount of functionality is what makes Allegro CTMS the ideal system for sites who wish to gain better visibility and control of their studies, while pursuing clinical research operations excellence. Allegro CTMS is a cloud-based clinical trial management system that manages the operational data of small to mid-sized research sites.
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. IBM Clinical Development ist eine einzige, skalierbare Cloud-basierte Plattform, die es klinischen Forschungsprofis ermöglicht, Studien zu erstellen und zu verwalten.
Allows for the collection and management of a wide variety of different types of data for applied behavior analysts. Allows for the collection and management of a wide variety of different types of data for applied behavior analysts.
For organizations engaged in conducting clinical trials, BioClinica CTMS clinical trial management software create a natural next step to bring Office tools, business process workflow, and documents into the regulated world. CTMS used to create a natural next step to bring Office tools, business process workflow, and documents into the regulated world.
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). Intuitive web-based platforms and on-line database applications for the design and management of clinical trials and registries.
Entrypoint i4 is a complete web-based system for creating, deploying, and administering custom data entry applications, providing data entry access anywhere you are. Entrypoint i4 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 complete system for creating, deploying, and administering custom data entry applications .
Our CTMS software is easy to operate, thereby saving you time and costs. The software adapts to your requirements, and not the other way around. BSI CTMS seamlessly integrates into your system environment, interfacing all necessary peripheral systems as a cloud or on-premise solution. This makes BSI CTMS the central hub for all aspects of your clinical trials. BSI CTMS covers all aspects of clinical trial management. It is the most intuitive and flexible system on the market. Test us out.
Nucleus is a platform that combines all aspects of clinical development into one convenient location, allowing you and your team to manage documents, communicate with one another and access your clinical information from the same application. Nucleus provides a cost-effective hub for clinical information (documents, communication, and technologies) to enhance collaboration.
Progeny Clinical simplifies the process of managing pedigree and family history data, used by genetic counselors, clinicians and research institutions worldwide. Use online family history questionnaires to collect patient data before the clinic visit. Assess risk for hereditary cancers, order/track genetic testing and results, run custom reports, generate patient letters, integrate with your EMR and much more. Plans include pre-configured free version to fully customizable premium options. Pedigree, family history and risk assessment software used by genetic counselors, clinicians and researchers.
Since 1993, Seattle-based StudyManager has been an industry-leading provider of Clinical Trial Management Software (CTMS) solutions to organizations who conduct clinical trial research. StudyManager Reveal, our Site CTMS solution, helps Sites and Hospitals organize and centralize clinical research through groundbreaking ease-of-use, power, and flexibility. Solution for research sites, universities, and hospitals streamlines clinical research, providing real-time access to key metrics.
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. 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. A solution that enables bio-pharma and clinical research organisations to capture critical patient related details for clinical trials.
Cloudbyz offers Clinical Trial Management on Salesforce 1 cloud platform for sponsors, clinical research organizations (CRO), hospitals and medical centers. CTM on Salesforce 1 cloud platform for sponsors, clinical research organizations (CRO), hospitals and medical centers.
Axiom Real-Time Metrics, is a leading eClinical technology and data management services provider offering cost-effective, unified EDC/DM tools focused around the unique needs and budgets of small-to-mid size device and biotech companies, CROs, Universities and Institutions. Axiom is unique to the marketplace in that we offer more functionality and tools in one easy-to-use unified platform, at a cost-competitive price, than any other EDC provider in the space. 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. QlikView puts information at your fingertips and frees you to make quick decisions, giving you intelligence you need to act faster.
MasterControl Inc. produces software solutions that enable regulated companies to get their products to market faster, while reducing overall costs and increasing internal efficiency. MasterControl securely manages a company's critical information throughout the entire product lifecycle. Learn why over 1000 companies have chosen MasterControl to automate their CAPA, document control, change control, training, audit management, and other quality management and regulatory processes. Software to help manage all tasks and documentation within clinical trials.
Flex Databases is a company providing e-solutions for clinical trials. We offer a unique platform which allows combining traditional features related to management of clinical trials (CTMS, EDC&IWRS) with the functionality for running internal pharma companies and CRO processes as well as a capability to manage financial data, invoicing and expenses. All modules developed by Flex Databases are validated and 21 CFR Part 11 compliant. Flex Databases is a company providing e-solutions for clinical trials.
iMedNet eClinical delivers an innovative, cost-effective, and easy-to-use technology platform that allows non-technical research personnel to quickly build their own clinical studies...in just a matter of days, not months. And iMedNet's low Software-as-a-Service (SaaS) pricing makes it affordable for ALL study types. iMedNet eclininical has been built from the ground up based on MedNet Solution's proven, decade-long experience developing practical eClinical solutions for sponsors and CROs. 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. Enable researchers to collect, interpret and distribute cardiac safety and clinical data accurately and efficiently.
Web based LIS platform enabling automated sequencing genotyping in a molecular diagnostic, clinical research environment. Web based LIS platform enabling automated sequencing genotyping in a molecular diagnostic, clinical research environment.
The premier EDC clinical trial software, eCaseLink combines novel technology and unmatched industry experience to help reduce clinical trial time, improve accuracy, drive down costs/improve ROI, prevent risk, and use clinical trial data more effectively. The most successful clinical trials begin and end with the highest quality, clean data. Data that is collected in the most streamlined and efficient way possible. An EDC system is a computerized system designed for t DSGs award-winning eCaseLink software is the most advanced Electronic Data Capture (EDC) solution in the industry.
Data management software for clinical trials that is based on GCP and regulatory compliance, user friendliness, and affordability. 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. Helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development.
Cloud-based solution that allows life science companies to manage clinical trial process providing clinical trial activities planning, tracking and control. Cloud-based solution with clinical trial activities planning, tracking and control for life science organizations.
A web-based data management solution that can be used for recruiting patients and managing all aspects of data associated with clinical research. A web-based solution that can be used for recruiting patients and managing all aspects of data associated with clinical research.
Dedicated to provide leading edge solutions and equipment purpose designed for clinical trial materials packaging. 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! SimpleTrials is a Clinical Trial Management System for Sponsors, CROs and Sites. Plans start at $35/month with no long term commitment
Siebel Clinical Trial Management System accelerator designed to help life sciences organizations manage all aspects of clinical trials efficiently and effectively. Solution designed to help life sciences organizations manage all aspects of clinical trials efficiently and effectively.
Octalsoft Clinical Trails Management System provides a single, centralized system to manage sponsor and CRO study management activities. Clinical trail management system that provides a single, centralized system to manage sponsor and CRO study management activities.
Software that provides document routing, submission tracking, protocol deviation review, and strict data access control, Software that provides document routing, submission tracking, protocol deviation review, and strict data access control,
Clinical data management solution with data queries generation, audit trails, electronic signatures, and data reconciliation tools. Clinical data management solution with data queries generation, audit trails, electronic signatures, and data reconciliation tools.
The DATATRAK ONE Unified Experience removes clinical research complexities, accelerating the ultimate outcome of every trial. The inherent strength of DATATRAK solutions is the intrinsic connection to the DATATRAK ONE platform, with all products powered by a single data source, providing unsurpassed system reliability, eliminating integration and downtime, and delivering an unsurpassed easy-to-use interface. These attributes deliver better site compliance, better data, and a safer trial. The DATATRAK ONE Unified Experience removes complexities, activating better site compliance, better data, and safer 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. Cronos has a complete solution for a clinical research organization conducting clinical trials and EDC solution for BA-BE studies.
Catalyst is a secure, cloud based Clinical Trials Management solution that enables clinical researchers to increase engagement with study participants while minimizing time spent managing bloated technology. Built with simplicity in mind, Catalyst can either be used as a standalone solution or it can easily integrate with other systems allowing researchers to continue using complimentary web based software they value. Secure, web based CTMS for research teams who want to easily interact with patients. Features include onboarding and study management.
Designed specifically for the communication needs and compliance requirements of life sciences and research facilities, Path Clinical reduces costs and maximizes efficiency by quickly connecting trial investigators in any location to improve retention and increase compliance. 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 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. A disruptive big data SaaS platform, that accelerates new drug launches,lowers clinical trial costs, and enables RBM.
The "Astracore Clinical Trials System" is a cloud-based solution for your CRF or eCRF needs. Very quick to set up for your specific needs with many features, and readily customizable for any unique or specific features. Able to store supporting documents, images, audio and video. Can upload existing CRFs or data collection templates or start from scratch. Free and non-obligation custom configuration and trial available - just contact us for details. Cloud based computer system for entering, storing, extracting, analysing and reporting of Clinical Trials Data (eCRF)..
Are you tired of using a CTMS that is overcomplicated, has a poor user interface and costs way too much money? At Intrinsic, we solved these problems by developing an easy to use practical CTMS that is cloud based. Intrinsic has 4 key clinical software productsCTMS, eTMF, study portals, and investigator portalsthat help pharma companies more easily manage their trials and CROs. Each module can be purchased separately, or users can enjoy the benefits of an integrated suite of clinical systems. Are you tired of using a CTMS that is overcomplicated, has a poor interface and costs too much? Contact us to learn more.
Data+ is a revolutionary data management solution for clinical research. We deliver an all-in-one solution for research organizations - connecting the organization, researchers, and patients together. Our focus is on insights - to improve care, team and time management, and patient engagement as well as compliance using informative feedback. 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 An interactive environment for multimodal biosignal data processing and analysis in the fields of clinical research and life sciences
An intuitive eSource, lab routing, and CTMS solution for research sites. Using CRIO, sites can save favorite procedures; build own source templates; capture source data quickly and accurately; mark up labs; and share visits with their monitors for review. Recruiting helps manage patients and campaigns, and enables one-click calling and texting. Finances calculates receivables and invoiceables as the visits are being completed. We are a premium service at an affordable price. An electronic source data, lab routing and CTMS system built for clinical research sites.
Target Health eSource EDC is aimed at helping organizations of all sizes with all their clinical trials software needs. As "Champions of the Paperless Clinical Trial", our patented eSource EDC software suite goes beyond direct data entry and electronic data capture (EDC), to include a clinical trial management system (CTMS), eInformed Consent, ePRO (patient reported outcomes), and includes integrated RBM reports. Backed by a CRO, we are the one-stop-shop for your EDC needs. As "Champions of the Paperless Clinical Trial", the Target Health eSource EDC software suite facilitates clinical trials of all sizes!
Awarded The Most Innovative Fully Comprehensive Software Solution for Clinics, Salons and Spas! Clinic Software .com gives your entire company a 360-degree view of your customers, appointments and facilitates collaboration across your organization, helping you build strong customer relationships to run and grow your business. Grow Sales. Save Time. Get Organized. Start today! Businesses of all sizes succeed with ClinicSoftware .com Advanced Features. Everything you need, all in one place. ClinicSoftware.com provides 360-degree view of your customers to help you build a strong relationship with your customers and grow!
Clinical Assay Management Software is a unique system that provides a consistent approach to the collection, management, and integrity of all clinical research study data. Along with including a full documentation management solution, the Clinical Assay Management Software tracks and manages all data generated and ensures a single verifiable version for all clinical and analytical data sets. Clinical Assay Management provides a consistent approach to the collection & management of clinical research study data.
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. Centralized software which provides ways to manage, track, and document throughout the clinical trials process.
Clinion CTMS is new age Clinical Trial Management System developed by Clinion. CTMS has all the features required for the complete management of Clinical Trial, Post Marketing Studies and Public Health Studies. Clinion CTMS is new age Clinical Trial Management System developed by Clinion.
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! Offers integrated clinical data management, trial management and EDC functions in a single easy to use package.
Clinical trial management software has never been easier to use. Clinical Trial Administrator (CTA) is clinical trial management software that assists clinical research sites conducting research studies. It is also 21 CFR Part 11 compliant. If you are trying to manage a study, patients, recruitment, or finances, CTA helps you get it done. Clinical Trial Administrator assists you in making well-informed decisions. Think of it as your decision-making assistant. 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. Features include accrual reports, verification of entry criteria, multiple treatment arms, stratification. random block sizes. email confirmations, optional collection subject data Comprehensive and secure randomization software for clinical trials run entirely on the Internet.
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. Address diverse and demanding customer scenarios and web experiences, regardless of complexity, scale, and duration of a study.
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 Investigator's first choise EDC - eCRF for all types of clinical trials
Cloud based platform with unified apps to optimize workflow processes, site engagement and training for global clinical trials. Cloud based platform with unified apps to optimize workflow processes, site engagement and training for global clinical trials.
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). Data MATRIX is a company providing full-service data management services based on the in-house developed EDC/IWRS software.
KLINDAT is a next-generation electronic Case Report Form (eCRF) for the pharmaceutical, biotech & medical device industries. KLINDAT is a next-generation electronic Case Report Form (eCRF) for the pharmaceutical, biotech & medical device industries.
Software made with an objective. Using technology we wanted to provide better care for patients and increase the revenue of the service providers. We started looking for products do just that. Since we couldn't find one, we made SimplexHIMES. SimplexHIMES is a cloud-enabled Clinic management software that is highly configurable to suit any type of customer. The regional plugin provides local requirements and regulatory needs of any region. Enterprise level product that can scale up on demand. 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. Comprehensive eSource system for all the source data for clinical trials with source, regulation, and drug accountability.
Configurable CTMS that helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases. Configurable CTMS that helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases.
Phoenix CTMS is a modern web application combining capabilities of database software used in clinical research in one modular system: PRS (Patient Recruitment System), CTMS (Clinical Trial Management System), CDMS (Clinical Data Management System). This unmatched feature set is geared to support all operational and regulatory requirements of the clinical front end in academic research, at CROs (Contract Research Organisations) and hospitals conducting clinical studies of any phase. Powerful open source (LGPL) CTMS/CDMS/subject registry database system, created at Medical University of Graz.
The comprehensive AssessRx solution is designed to assess a clinicians ability to consistently and safely apply clinical knowledge, skills, and judgment through the use of multiple valid and reliable assessments. This solution helps organizations quickly identify a clinician's ability to recognize and respond to urgent patient situations as well as effectively communicate with others within the healthcare team. HealthStream Competency Center is competency-driven, healthcare specific, and a HealthStream-integrated competency management system.
Teamscope is an Electronic Data Capture (EDC) platform available on iOS and Android for clinical and field research. Build your studies using our point&click interface, generate real-time reports and keep your data secure and protected at all moments. Use Teamscope to collect data for clinical studies, even when you are offline or in remote areas.