Software de Gestión de Ensayos Clínicos

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Clinical Conductor CTMS es el sistema de gestión de ensayos clínicos (CTMS) diseñado para sitios de investigación, hospitales, AMC, redes de sitios, sistemas de salud y CRO. Clinical Conductor CTMS permite a las organizaciones que realizan investigación clínica ser más eficientes y rentables. Clinical Conductor CTMS es la aplicación líder en el mercado, ya que facilita el proceso de los ensayos clínicos y permite a las organizaciones tomar mejores decisiones comerciales y enfrentar cada desafío. Descubre más sobre Clinical Conductor CTMS Clinical Conductor es el sistema de gestión de ensayos clínicos (CTMS) líder diseñado para sitios de investigación, redes de sitios, hospitales, AMC, CRO y sistemas de salud. Descubre más sobre Clinical Conductor CTMS
MACRO es una solución de captura electrónica de datos basada en la nube que permite a los investigadores recopilar rápidamente información precisa y confiable para su análisis. MACRO se ajusta a las normas de calidad científica y ética para el diseño, la realización, el registro y la creación de informes de ensayos clínicos con sujetos humanos. Las funciones incluyen la creación de eCRF de autoservicio (creación de formularios), fácil exportación de datos, pistas de auditoría, gestión de usuarios y mucho más. Tiene certificación ISO 27001, cumple con las buenas prácticas clínicas (GCP) y la norma 21 CFR, cumple con las normas de accesibilidad WCAG2-AA. Descubre más sobre MACRO Captura electrónica de datos de Elsevier: potenciar la investigación clínica. Descubre más sobre MACRO
Un sistema de captura electrónica de datos, apto para dispositivos móviles, para ensayos clínicos, construido por investigadores para investigadores. Las características incluyen la creación de eCRF de autoservicio, aleatorización, ePro (encuestas de pacientes), supervisión, fácil importación y exportación de datos, importador de los datos de EHR (basado en HL7 FHIR), rastros de la auditoría, gestión de usuarios y mucho más. Cuenta con plena certificación ISO 27001, es conforme con las buenas prácticas clínicas (GCP) y el título 21 de CFR y proporciona servidores en EE. UU. (de conformidad con HIPAA), el Reino Unido, Holanda y Alemania. Descubre más sobre Castor EDC El único sistema compatible con GCP y 21 CFR que es accesible para todos los investigadores y tiene todas las características de los sistemas caros. Empieza ahora. Descubre más sobre Castor EDC
Los protocolos son complejos. Obtener datos no debería serlo. Con un diseñador de estudios colaborativo, con función de arrastrar y soltar, y formularios compatibles con dispositivos móviles para tus sitios y asuntos, OpenClinica es más que solo captura de datos. Es una mejor experiencia. ¿El resultado? Datos de mayor calidad para tu estudio, a un bajo costo que también facilita la generación de presupuestos. Con cada implementación: alojamiento en la nube seguro y de alto rendimiento en AWS | Validación documentada | Cumplimiento con FDA, EMA, GDPR e HIPAA Descubre más sobre OpenClinica Diseño de estudios, EDC, ePRO, IxRS y visualizaciones de datos enriquecidos, todo en una única plataforma fácil de usar. Es tu información clínica, administrada. Descubre más sobre OpenClinica
Smartsheet, an online work execution platform, empowers pharmaceutical companies and clinical research organizations to track, manage, and report on clinical tests and trials. With its familiar spreadsheet format, Smartsheet enables teams to easily get started and effectively collaborate. Securely share, store, and access PHI while meeting HIPAA's regulatory requirements. Plus, real-time dashboards allow you to spend less time on the process and more time delivering results. Descubre más sobre Smartsheet Smartsheet is an online work execution platform empowering organizations of all sizes to plan, manage, automate, and report on work. Descubre más sobre Smartsheet
Data+ es una plataforma totalmente compatible y personalizable para aplicaciones de salud y ciencias de la vida. Amplía las capacidades de tus sistemas principales a través de una amplia gama de aplicaciones para la gestión de datos clínicos, el desarrollo de medicamentos, la gestión de laboratorios y mucho más. Elige una aplicación preparada para configurar o crea una nueva desde cero con el diseñador visual intuitivo. Capacita a los usuarios no tecnológicos para que creen soluciones sobre la marcha y resuelvan los problemas en el momento en que surjan, aliviando la carga del área de TI. Descubre más sobre Data+ Platform Data+ es una plataforma totalmente compatible y personalizable para aplicaciones de salud y ciencias de la vida. Descubre más sobre Data+ Platform
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. produce soluciones de software que permiten a las empresas reguladas comercializar sus productos más rápidamente, al tiempo que reducen los costos generales y aumentan la eficiencia interna. MasterControl administra de forma segura la información crítica de una empresa a lo largo de todo el ciclo de vida del producto. Descubre por qué más de 1000 compañías han elegido MasterControl para automatizar su proceso CAPA, control de documentos, control de cambios, capacitación, gestión de auditoría y otros procesos regulatorios y de gestión de la calidad. Software para ayudar a gestionar todas las tareas y documentación dentro de los ensayos clínicos.
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.
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! Research sites & networks looking to streamline study information and company processes. We guide customers from study start to finish.
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. Manage, distribute and optimize your content across premium publishers through 25+ social, native and content discovery partners.
Medrio ofrece a los investigadores clínicos una solución de captura electrónica de datos (EDC) eficiente y fácil de usar, así como un conjunto de aplicaciones nativas para tabletas para fuentes electrónicas y resultados informados por pacientes por vía electrónica (ePRO). Este software está completamente alojado en la nube, no requiere programación para la compilación del estudio o cambios a mitad del estudio, y permite a los patrocinadores de ensayos clínicos y CRO de todo tipo reducir los costos de sus estudios. Desde la fundación de esta solución, la han utilizado cientos de organizaciones de las áreas farmacéutica, dispositivos médicos, diagnóstico y salud animal. Medrio proporciona soluciones clínicas electrónicas que son rápidas y fáciles de usar y no requieren programación.
Clinical Studio es un verdadero producto SaaS (Software-as-a-Service) basado en la nube, compuesto por un software diseñado específicamente para transformar la investigación clínica, lo que permite a las empresas completar los ensayos de forma eficiente en un sistema compatible con 21 CFR Parte 11. Clinical redefine el software de investigación clínica mediante el aprovechamiento de software integrado y aplicaciones móviles nativas para agilizar el diseño, el despliegue y la gestión de los estudios clínicos. Clinical Studio facilita la investigación mediante la entrega de infraestructura empresarial a pedido, por una tarifa fija.
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. Ripple facilitates the recruitment and management of patients for clinical and translational studies.
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.
La misión del equipo de ClinCapture es construir software que salve vidas. Su tecnología reduce el costo de los ensayos clínicos al simplificar los procesos de captura de datos al tiempo que proporciona una plataforma que protege la privacidad del paciente. ClinCapture avanza en la evaluación y el desarrollo de medicamentos, productos biológicos y dispositivos que son prometedores para el diagnóstico y/o tratamiento de una amplia gama de enfermedades o afecciones médicas. ¡Solicita una demostración hoy mismo! ClinCapture proporciona a todos sus clientes una nube privada EDC, para que tu privacidad esté siempre protegida. ¡Solicita una demostración hoy mismo!
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!
La solución para investigación clínica STARLIMS crece a medida que las necesidades de los laboratorios evolucionan, lo cual ofrece una flexibilidad sin igual y soporte de flujos de trabajo configurables por el usuario para una amplia gama de proyectos de investigación, ensayos clínicos y procesos de laboratorio. Permite al usuario sentir confianza en su capacidad para satisfacer las cambiantes necesidades de los investigadores y cumplir con las regulaciones cada vez más estrictas, a la vez que permite proporcionar resultados de investigación precisos. La solución para investigación clínica STARLIMS asegura que las muestras de laboratorio se recojan, manejen y procesen con precisión con la solución.
¡Galardonada la solución de software más completa e innovadora para clínicas, salones y spas! Clinic Software.com le brinda a toda tu empresa una visión de 360 grados de tus clientes, citas y facilita la colaboración en toda tu organización, lo que te ayuda a establecer relaciones sólidas con los clientes para administrar y hacer crecer tu negocio. Aumenta las ventas. Ahorra tiempo. Organízate. Empieza hoy. Empresas de todos los tamaños triunfan con ClinicSoftware.com Características avanzadas. Todo lo que necesitas, en un solo lugar. ¡ClinicSoftware.com brinda una vista de 360 grados de tus clientes para ayudarte a construir una relación sólida con tus clientes y crecer!
Solución para la gestión de ensayos clínicos (CTMS) robusta y flexible, basada en SaaS, entregada a los patrocinadores o las CRO. La funcionalidad incluye: * gestión de proyectos; * suministros; * seguimiento de CRF y DCF; * portal del patrocinador y el investigador; * pagos clínicos; * planilla de tiempo y gastos; * informes de supervisión; * seguimiento de EAS; * cliente fuera de línea. Solución amplia, flexible y modular de CTMS para patrocinadores o CRO pequeños o medianos.
Sistema flexible de captura electrónica de datos (EDC) y sistema de gestión de datos para ensayos clínicos, investigación epidemiológica, aleatorización web (IWRS), registros de pacientes, ePRO y encuestas web. Este software proporciona la interfaz más fácil de usar e intuitiva del mercado con características y opciones de diseño no disponibles en otros productos de software. Captura electrónica de datos (EDC) flexible y fácil de usar basada en la web y sistema de gestión de datos para ensayos clínicos e investigación.
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. ClinPlus CTMS - Designed specifically to help organizations overcome the technical challenges associated with managing clinical trials.
Clinical Assay Management Software es un sistema exclusivo que proporciona un enfoque de uniformidad en la recopilación, gestión e integridad de todos los datos de estudios de investigación clínica. Junto con la inclusión de una solución de gestión de documentación completa, el software Clinical Assay Management Software rastrea y administra todos los datos generados y garantiza la existencia de una versión única y verificable de todos los conjuntos de datos clínicos y analíticos. Clinical Assay Management Software proporciona un enfoque de uniformidad en la recopilación y gestión de los datos de estudios de investigación clínica.
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.
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.
For automating environmental, public health, clinical/toxicology, utility, process control and related laboratories. For automating environmental, public health, clinical/toxicology, utility, process control and related laboratories.
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.
Agiliza la entrada de datos clínicos en papel y proporciona acceso a datos en tiempo real y una calidad de datos mejorada. Agiliza la entrada de datos clínicos en papel y proporciona acceso a datos en tiempo real y una calidad de datos mejorada.
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.

Por Almac Clinical Technologies

(2 opiniones)
Electronic data capture platform that provides the recording of patient-reported outcome data through a centralized database. Electronic data capture platform that provides the recording of patient-reported outcome data through a centralized database.
Since 1992, DFdiscover has been in use by CROs, Pharmaceuticals/Medical Device companies, and Global Health Organizations for the past 28 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 or an enterprise license. DFdiscover is a mature and stable EDC Clinical Trial System, that is a true hybrid system.
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.
Ethical eAdjudication para la adjudicación de terminales clínicos es un servicio de software administrado por GxP basado en una plataforma en la nube diseñada para apoyar a los líderes de estudio, los miembros del comité y el personal de control de calidad en toda la revisión central y adjudicación de puntos finales subjetivos. Proporciona las herramientas/servicios adecuados para llevar a cabo la revisión independiente y procedimientos de adjudicación de manera oportuna, efectiva y de calidad controlada. Servicio de software de adjudicación de terminales en la nube. Diseñado para el cumplimiento y eficacia de GxP
IBM Clinical Development de Watson Health es una solución SaaS global que puede ayudar a las ciencias humanas a transformar la investigación clínica y puede acelerar la entrega de terapias necesarias a los pacientes. Con un potente sistema de captura electrónica de datos (EDC) en su núcleo, el desarrollo clínico de IBM ofrece a los investigadores clínicos acceso a información velada y visibilidad de los datos de prueba. Escalable tanto en características como en funcionalidad, ofrece una serie de capacidades robustas que se pueden adaptar a todos los ensayos clínicos. IBM Clinical Development es una única plataforma escalable en la nube que permite a los profesionales de investigaciones clínicas diseñar y gestionar ensayos.
Clinical trial tool that enables leveraging of family health history through risk assessment and diagnosis. Clinical trial tool that enables leveraging of family health history through risk assessment and diagnosis.
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.
A comprehensive clinical research management information system. A comprehensive clinical research management information system.
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.
Easy to custom and to use, fully integrated with IVRS and DSM. Easy to custom and to use, fully integrated with IVRS and DSM.
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.
Software fácil de usar, diseñado para registrar y analizar el rastreo de animales dentro de un actímetro IR. Software fácil de usar, diseñado para registrar y analizar el rastreo de animales dentro de un actímetro IR.
Catchtrial is a simple, cloud-based platform for capturing clinical trial data and images. Accessible anytime, anywhere, Catchtrial puts key information at your ngertips, resulting in shorter response times, improved compliance, and reduced costs. Catchtrial is a simple, cloud-based platform for capturing clinical trial data and images.
Clinical data management system with streamlined study creation approach and detailed reporting. Clinical data management system with streamlined study creation approach and detailed reporting.
Agile Health Computing's application, MAISi, is a user-friendly and sophisticated Clinical Trial Management System designed to answer the management needs of clinical research sites. By collecting and monitoring research sites clinical trial business metrics, MAISi facilitates better protocol implementation and better time and financial management which is essential in this competitive international market. MAISi is a user-friendly and sophisticated Clinical Trial Management System that has been designed to assist clinical research sites.
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.
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. Learn more at iqvia.com. DrugDev, now part of IQVIA offer the worlds first unified clinical operations suite for Design & Planning, eConsent, Trial Management
Pristima es una solución empresarial totalmente integrada para la gestión de datos preclínicos que ofrece automatización completa del ciclo de vida y asistencia para la gestión de estudios de investigación en farmacología y seguridad de medicamentos, gestión de vivarios y atención veterinaria. Desde la cría y el pedido hasta el proceso de envío del estudio, el paquete de Pristima gestiona la planificación y el registro de datos, controla los cambios autorizados y recopila los datos para enviarlos a las agencias reguladoras. El paquete de Pristima® es una plataforma de software para estudios preclínicos totalmente integrada que ofrece una automatización completa del ciclo de vida para el descubrimiento de fármacos.
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.
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.
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.
DataFinch Technologies is a software company on a mission to provide the most comprehensive and state-of-the-art technological solutions for behavior analysts working with special needs communities. Our flagship product, CATALYST, is the premier and most robust electronic data collection system available to ABA professionals. Data collection software for Applied Behavior Analysis professionals working with individuals with autism and other special needs.
Monitor / manage clinical studies and bring clinical research programs to a successful conclusion. Ensure compliance with FDA's regulatory constraints and recommendations. Ennov CTMS offers both clinical trial monitoring and multi-study supervision. Visibility and decision support make you more effective. Monitor and manage clinical studies with a full web interface. Integrated to Ennov's Clinical Platform (eTMF, EDC, CDMS...).
Clinion CTMS is the new age Clinical Trial Management system, which allows you to efficiently manage multiple clinical studies and obtain real time information about recruitment across sites, SAE / AE reporting, Budgeting, Expenses and invoicing, Scheduling and monitoring of sites, site reports etc. Clinion-CTMS is flexible, scalable and integrated cloud based web application available as SaaS (Pay as you use) model. Manage multiple clinical trials efficiently and obtain real time information on key clinical trial parameters at your fingertips

Por SigmaSoft International

(0 opiniones)
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.

Por TrialStat!

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

Por Clinipace

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

Por Winchester Business Systems

(0 opiniones)
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.

Por Aris Global

(0 opiniones)
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.

Por MAJARO InfoSystems

(0 opiniones)
Comprehensive SAS based clinical data management, EDC, and clinical trials reporting system Comprehensive SAS based clinical data management, EDC, and clinical trials reporting system

Por Phoenix Software International

(0 opiniones)
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 complete system for creating, deploying, and administering custom data entry applications .

Por QuesGen Systems

(0 opiniones)
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.

Por POPSI CUBE

(0 opiniones)
Electronic pen and paper technology for clinical research / CRO. Electronic pen and paper technology for clinical research / CRO.

Por InfoEd International

(0 opiniones)
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.
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.

Por Trial by Fire

(0 opiniones)
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

Por Databean

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

Por Fortress Medical Systems

(0 opiniones)
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.

Por HEKA Instruments

(0 opiniones)
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.
Clinical Research Organization with extensive experience in conducting Clinical Trials. Clinical Research Organization with extensive experience in conducting Clinical Trials.

Por Cambridge Cognition

(0 opiniones)
Cognitive assessment and neurotechnology products accelerating clinical development from proof of concept to post-marketing. We are the leading providers of validated touchscreen cognitive tests for clinical trials developing medicines that are safe and effective in the human brain. Cognitive assessment and neurotechnology products accelerating clinical development.

Por Octalsoft

(0 opiniones)
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.

Por Precyse Solutions

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

Por Interrand

(0 opiniones)
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.

Por SCAD Software

(0 opiniones)
Regulatory Management System that manages and monitors the regulatory side of a clinical trial. Fully-integrated, web-based solution that manages and monitors the regulatory side of a clinical trial.

Por Ofni Systems

(0 opiniones)
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.

Por SyMetric Systems

(0 opiniones)
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.

Por iWeb Technologies

(0 opiniones)
Set of modules that help all stakeholders effectively manage all areas of clinical and research management. Set of modules that help all stakeholders effectively manage all areas of clinical and research management.

Por DATATRAK

(0 opiniones)
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.

Por Sarjen System

(0 opiniones)
BizNET, software de gestión de ensayos clínicos, ofrece un conjunto integrado de productos de software para las organizaciones de investigación por contrato (CRO), el sector farmacéutico, los sectores biotecnológicos y el sector de dispositivos médicos. Esta solución combina diversos módulos integrados que respaldan de forma destacada las actividades de ensayos clínicos, como la recolección de datos EDC/DDC, gestión de la aleatorización de fármacos y sistema de respuesta web interactiva (IWRS) y modelo de tabulación de datos de estudio (SDTM) del CDISC. Es un software validado, que cumple con la parte 11 de 21 CFR y las pautas de buenas prácticas clínicas (GCP) que proporcionan un proceso transparente y sin problemas para la regulación. Para proyectos de investigación clínica: gestión de proyectos, evaluación de viabilidad, inscripción, captura de datos, compilación, archivado.

Por Infoset

(0 opiniones)
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

Por Webosphere

(0 opiniones)
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.

Por Parallel6

(0 opiniones)
Solución basada en la nube para líderes de ensayos clínicos. Las características incluyen inscripción digital, participación de los miembros y creación de informes. Solución basada en la nube para líderes de ensayos clínicos. Las características incluyen inscripción digital, participación de los miembros y creación de informes.

Por Nextrials

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

Por Data MATRIX

(0 opiniones)
Data MATRIX es una empresa que ofrece servicios completos de gestión de datos basados en el software EDC/IWRS desarrollado internamente. El EDC/IWRS ha sido utilizado en más de 150 ensayos internacionales y los datos se han enviado con éxito a EMA y FDA. Este software fácil de usar está completamente validado y cumple con todos los estándares del sector (CDISC, 21 CFR Parte 11). Data MATRIX es una empresa que ofrece servicios completos de gestión de datos basados en el software EDC/IWRS desarrollado internamente.

Por Cloudbyz

(0 opiniones)
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 Study Management Project & Milestone Management Budget Management Start-up Site Management Essential Document Checklist Subject Management Adverse Events Protocol Deviation eCRF Payments & Invoices Virtual Trial Patient Recruitment CTM on Salesforce 1 cloud platform for sponsors, clinical research organizations (CRO), hospitals and medical centers.

Por Catalyst eClinical

(0 opiniones)
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.

Por Axiom Real-Time Metrics

(0 opiniones)
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.
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.

Por Replior

(0 opiniones)
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.

Por Clinical Systems

(0 opiniones)
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.

Por EasyTrial

(0 opiniones)
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).

Por Comprehend Systems

(0 opiniones)
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

Por Clinical Data

(0 opiniones)
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.

Por VACAVA

(0 opiniones)
Gestiona documentos, firmas y fechas límite con facilidad. Comparte documentos de forma segura en cualquier lugar y en cualquier momento. RDMS cuenta con paneles de gestión de prueba y documentos, captura de firmas electrónicas conforme a la norma 21 CFR Parte 11, actualizaciones de datos dinámicos, llenado de formularios automático, notificadores de fechas límite e historial de cambios. Flexible y escalable, las soluciones VACAVA se proporcionan a través de la nube para que nunca tengas que preocuparte por los detalles tecnológicos. Redefinir el documento normativo de ensayos clínicos y la administración de TMF con una solución automatizada y personalizable que cumple con 21 CFR Parte 11.

Por Innovate Research

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

Por Astracore

(0 opiniones)
Una aplicación de captura electrónica de datos de ensayos clínicos disponible tanto como una aplicación móvil como a través de Internet, configurada rápidamente para tus necesidades. Rápido de configurar para tus necesidades específicas con muchas características. Capaz de almacenar documentos de asistencia, imágenes, audio y video. Puede cargar archivos CRF existentes o plantillas de recolección de datos o comenzar desde cero. Configuración y prueba personalizadas, gratis y sin compromiso: ponte en contacto para obtener más detalles. Sistema informático en la nube para introducir, almacenar, extraer, analizar e crear informes de datos de ensayos clínicos.

Por BSI Business Systems Integration AG

(0 opiniones)
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.

Por MEDAS

(0 opiniones)
Un potente sistema de gestión clínica con módulos de extremo a extremo como programación de citas, facturación, EMR y mucho más. Un potente sistema de gestión clínica con módulos de extremo a extremo como programación de citas, facturación, EMR y mucho más.

Por Trials.AI

(0 opiniones)
Trials.ai leverages artificial intelligence to manage clinical trials. Trials.ai leverages artificial intelligence to manage clinical trials.