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Castor EDC è una piattaforma di acquisizione dati in formato elettronico, basata sul cloud, che consente ai ricercatori di acquisire facilmente dati riutilizzabili di alta qualità. Le funzionalità includono creazione di eCRF self-service (creazione di moduli), randomizzazione, ePRO (sondaggi per i pazienti), monitoraggio, importazione e esportazione di dati, strumento di importazione dei dati EHR (basato su HL7 FHIR), audit trail, gestione degli utenti e molto altro ancora. Completamente certificato ISO 27001, è conforme a GCP e 21 CFR e fornisce server negli Stati Uniti (conformi a HIPAA), nel Regno Unito, nei Paesi Bassi e in Germania. Ulteriori informazioni su Castor EDC L'unico sistema conforme a GCP e 21 CFR conveniente per tutti i ricercatori, ma con tutte le caratteristiche dei sistemi più costosi. Inizia ora. Ulteriori informazioni su Castor EDC
Clinical Conductor CTMS è il sistema di gestione delle sperimentazioni cliniche (CTMS) progettato per siti di ricerca, ospedali, AMC, reti di siti, sistemi sanitari e CRO. Clinical Conductor CTMS consente alle organizzazioni che conducono ricerche cliniche di essere più efficienti e redditizie. Clinical Conductor CTMS è l'applicazione leader del mercato, che facilita il processo di sperimentazione, consentendo alle organizzazioni di prendere decisioni aziendali migliori e affrontare ogni sfida. Ulteriori informazioni su Clinical Conductor CTMS Clinical Conductor è il software CTMS leader del mercato per siti di ricerca, reti di siti, ospedali, AMC, CRO e sistemi sanitari. Ulteriori informazioni su Clinical Conductor CTMS
I protocolli sono complessi. Ottenere i dati non dovrebbe esserlo. Con un progettista di studi collaborativo e a trascinamento progettato per te e moduli ottimizzati per dispositivi mobili per i siti e i soggetti, OpenClinica è più di una semplice soluzione per la raccolta di dati. È un'esperienza migliore. Il risultato? Dati per lo studio di qualità superiore e dal costo ridotto che facilitano anche la gestione del budget. Con ogni distribuzione: hosting sicuro sul cloud sicuro e ad alte prestazioni su AWS | Convalida documentata | Conformità con FDA, EMA, GDPR e HIPAA Ulteriori informazioni su OpenClinica Progettazione dello studio, EDC, ePRO, IxRS e visualizzazioni di dati utili, il tutto su un'unica piattaforma facile da usare. Questi sono i dati clinici dell'utente gestiti. Ulteriori informazioni su OpenClinica
Smartsheet è una piattaforma di esecuzione del lavoro online che consente alle aziende farmaceutiche e alle organizzazioni di ricerca clinica di monitorare, gestire e creare report su test clinici e sperimentazioni. Grazie al suo familiare formato di foglio di calcolo, Smartsheet consente ai team di iniziare facilmente un progetto e collaborare in modo efficace. Potrai condividere, archiviare e accedere in modo sicuro alle PHI rispettando i requisiti normativi HIPAA. Inoltre, le dashboard in tempo reale consentono di dedicare meno tempo al processo e più tempo a fornire risultati. Ulteriori informazioni su Smartsheet Smartsheet è una piattaforma di esecuzione del lavoro online che consente alle organizzazioni di tutte le dimensioni di pianificare, gestire, automatizzare e generare report sul lavoro. Ulteriori informazioni su Smartsheet
Caspio è una piattaforma per la creazione di applicazioni per database online che non necessita di competenze di programmazione. Classificata come leader da Forrester Research, la piattaforma multifunzione offre tutto il necessario per trasformare digitalmente le attività e i flussi di lavoro d'impresa. Include database integrato sul cloud, costruttore di applicazioni visive, sicurezza di livello aziendale, conformità normativa e infrastruttura globale scalabile. Scopri perché Caspio è considerato affidabile da oltre 12.000 aziende in tutto il mondo. Provalo gratuitamente. Ulteriori informazioni su Caspio Caspio è una piattaforma per la creazione di applicazioni per database online che non necessita di competenze di programmazione. Ulteriori informazioni su Caspio
Research Manager agevola coloro che sono impegnati nella ricerca nelle scienze biologiche con una piattaforma di ricerca online per tutto ciò che riguarda la ricerca e le registrazioni. La piattaforma funge da punto centrale in cui ricercatori, coordinatori della ricerca e comitati etici possono accedere a servizi e informazioni e consente loro di sviluppare e migliorare ulteriormente i dati. Inoltre, Research Manager offre esperienza in materia di raccolta, convalida e arricchimento dei dati. Ulteriori informazioni su Research Manager Aggiunta di valore ai dati. Research Manager offre una piattaforma di ricerca in cui sono integrati la gestione dei processi e la raccolta dei dati. Ulteriori informazioni su Research Manager
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Il software eReconciliation consente di importare e comparare i record da qualsiasi database clinico e di sicurezza, segnala i cambiamenti nei dati di origine e offre funzioni operative che aiutano a gestire tutte le operazioni di riconciliazione. Tutte le operazioni sono registrate in un audit trail e possono essere esportate in file Excel. Ulteriori informazioni su eReconciliation eReconciliation® è una soluzione completa, che supporta tutte le operazioni relative alla riconciliazione SAE. Ulteriori informazioni su eReconciliation
Cloud Platform è un insieme di servizi modulari basati sul cloud che ti consentono di creare qualsiasi componente, da semplici siti web ad applicazioni complesse. Cloud Platform è un insieme di servizi modulari basati sul cloud che ti consentono di creare qualsiasi componente, da semplici siti web ad applicazioni complesse.
Snappii mette a disposizione molte app mobili per il settore farmaceutico come soluzione mobile conveniente e facile da usare che consente di risparmiare tempo ed evita procedure inutili, rende più facile condividere le informazioni sui farmaci tra i farmacisti, elimina gli errori dovuti al fattore umano e permette una raccolta di dati rapida e accurata. Gli utenti delle app possono caricare, modificare e condividere i propri PDF. Scegli tra oltre 400 app già pronte oppure chiedi di creare l'app più adatta alle tue esigenze. Snappii è una società leader nella creazione di app mobili e app per i moduli. Le app aziendali di Snappii sono utilizzate da circa 500.000 persone di oltre 30 settori.
Medrio offre ai ricercatori clinici una soluzione di acquisizione di dati in formato elettronico (EDC) efficiente e facile da utilizzare, oltre a una suite di applicazioni native per tablet per eSource ed ePRO. Questo software è completamente basato sul cloud, non richiede alcuna programmazione per la creazione degli studi o la modifica intermedia degli stessi e consente agli sponsor delle sperimentazioni cliniche e alle CRO di ogni tipo di ridurre i costi degli studi. Fin dalla loro creazione, queste soluzioni sono state impiegate da centinaia di organizzazioni che operano nel settore farmaceutico, dei dispositivi medici, della diagnostica e della salute degli animali. Medrio offre soluzioni eClinical veloci e facili da utilizzare che non richiedono programmazione.
RealTime Software Solution è leader globale nei sistemi di gestione delle sperimentazioni cliniche (Clinical Trials Management System, CTMS), basati su SaaS, per centri, sponsor e CRO. RealTime è anche l'unico fornitore di CTMS in grado di offrire una suite di soluzioni completa in una piattaforma lineare: Site Operations Management System (SOMS), il sistema di gestione delle operazioni dei centri. SOMS include CTMS, SitePAY, TEXT, eDOCS ed eSOURCE, tutti strumenti leader del settore, accessibili tramite un'applicazione mobile di facile utilizzo. RealTime offre anche una soluzione di livello enterprise per centri di grandi dimensioni e reti di centri. Centri di ricerca e reti di centri che desiderano semplificare le informazioni degli studi e i processi aziendali. Accompagna i clienti dall'inizio alla fine degli studi.
Ripple is a highly-secure, web-based recruitment-focused patient and study management tool for clinical and translational studies. Ripple streamlines and centralizes your study processes and manages 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.
Clinical Studio è un vero prodotto SaaS (Software-as-a-Service) basato sul cloud comprendente un software appositamente sviluppato per trasformare le ricerche cliniche. Consente alle aziende di completare in modo efficiente le sperimentazioni su un sistema conforme alla norma 21 CFR Parte 11. Clinical Studio ridefinisce il software per le ricerche cliniche sfruttando il software integrato e le applicazioni mobili native per semplificare la progettazione, la distribuzione e la gestione degli studi clinici. Clinical Studio facilita la ricerca fornendo un'infrastruttura aziendale on-demand a pagamento.
The EDGE programme is embedded across 80% of the NHS within the UK, as well as being utilised across the globe. EDGE provides users with faster access to real-time data and gives complete study management from start to finish. It offers collaborative features which increases efficiency and allows more time for clinical staff to be spent with patients. We offer flexible pricing based upon your organisation type and size. Email [email protected] for more info or to request a free demo. A global, innovative, cloud-based clinical trial management system providing faster access to real-time data.
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.
ClinCapture provides a powerful eClinical platform that enables sponsors and CROs to rapidly build and deploy studies, lower clinical trial costs, and streamline data capture processes. Offering a host of private cloud solutions, ClinCapture¿s technologies help advance 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! ClinCapture provides all of its customers with Private Cloud EDC, so your privacy is always protected. Request a demo today!
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.
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.
Clinics of all sizes succeed with ClinicSoftware.com Looking for a CRM Software alternative? Two steps ahead. Make running your business Smarter, Better, Faster. Instantly. ClinicSoftware.com is a full suite of tools in cloud based created to help companies and appointment-based businesses of any industry and size such as Clinics, Spas and Salons to Grow Sales, Save Time & Get Organized. Awarded The Most Innovative Software in the industry, 98% of customers recommend ClinicSoftware.com Looking for a CRM Software alternative? Two steps ahead. Make running your business Smarter, Better, Faster. Instantly.
Veeva Vault is a true cloud enterprise content management platform and suite of applications specifically built for life sciences. Veeva Vault is the only content management platform with the unique capability to manage both content and data. Because all Vault applications are built on the same core platform, companies can ease the flow of documents across regions and departments, eliminating system, site, and country silos and streamlining their end-to-end clinical processes. Veeva Vault is a true cloud enterprise content management platform and suite of applications specifically built for life sciences.
Teamscope is the worlds easiest to use data collection app for clinical and field research. With Teamscope you can build powerful forms with branching logic, data validation and automatic calculations. Use mobile forms to collect data without the need for an internet connection. Create cases, share them with your team and capture data across time. Keep your data secure at all moments with a passcode and data encryption. Create powerful mobile forms, collect data offline and visualize it with a few clicks.
MACRO è una soluzione di acquisizione di dati in formato elettronico, basata sul cloud, che consente ai ricercatori di raccogliere rapidamente dati precisi e affidabili per l'analisi. MACRO è conforme con standard di qualità etici e scientifici per la progettazione, la conduzione, la registrazione e la creazione di report per studi clinici su soggetti umani. Le sue funzionalità includono: creazione di eCRF self-service (creazione di moduli), esportazione facile di dati, monitoraggio delle ispezioni, gestione degli utenti e molto altro ancora. Certificata ISO 27001, GCP e conforme al titolo 21 CFR e agli standard di accessibilità WCAG2-AA. Acquisizione di dati in formato elettronico da Elsevier: potenziamento della ricerca clinica.
Prelude is small biotech's best friend. With the VISION eClinical database, and our team of certified data managers, you no longer need to hire costly CROs or outsourced data managers. When you work with Prelude, we become an extension of your clinical team, providing the industry's best technical service and software to reduce costs and resources required for studies of all phases. Our software, together with our mobile ePro app, make remote studies more possible than ever. Prelude is small biotech's best friend. No need to hire the expensive CRO when you work with Prelude and our VISION software.
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!
Abbott Informatics' solutions simplify the complexity of your entire product lifecycle management process. Easy-to-use and adaptable to your organizations needs, the STARLIMS brand of informatics solutions support the rapidly changing data management needs across your organization. Our solutions can integrate with your current systems, while also identifying opportunities to improve processes so you can bring high quality and safe products to market faster. From R&D to manufacturing to quality compliance, Abbott Informatics' solutions support your entire product lifecycle.
Visual Planning is a collaborative planning & scheduling software used to manage all types of resources. Our unique flexibility allows you to track projects, jobs, tasks, customers, work orders, employees, equipment and more in a single tool, so you can focus on what truly matters. Centralizing data helps teams become more efficient. Users can work in collaboration from anywhere and access on mobile devices. Send e-mails/SMS alerts to team members, and connect schedules with personal calendars. Collaborative visual scheduling & planning software to track all types of resources, robust and user-friendly.
SureClinical designs, develops and delivers innovative life science cloud applications that help streamline and accelerate the delivery of new drugs, therapies and treatments to patients worldwide. With SureClinical, clinical teams can go digital, eliminating paper-based and manual processes to pursue the fastest path to clinical trial success. Health sciences cloud applications used to accelerate innovative therapies.
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 Cloud-based clinical trial management solution that allows businesses to store information, generate reports, secure data, and more.
Data+ è una piattaforma completamente conforme e personalizzabile per le applicazioni dedicate a salute e scienze naturali. Questa soluzione consente di estendere le funzionalità dei sistemi principali tramite un'ampia gamma di applicazioni per la gestione dei dati clinici, lo sviluppo di farmaci, la gestione dei laboratori e altro ancora. Scegli un'applicazione pronta per la configurazione o creane una nuova da zero utilizzando un intuitivo strumento di progettazione visivo. Consenti agli utenti non esperti di tecnologia di creare rapidamente soluzioni e risolvere i problemi nel momento in cui si presentano, alleviando il carico di lavoro del reparto IT. Data+ è una piattaforma completamente conforme e personalizzabile per applicazioni dedicate a salute e scienze naturali.
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
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. Flexible, user-friendly, web-based electronic data capture (EDC) and data management system for clinical trials and research.
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.
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.
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.
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.
The only CDMS designed for seamless support of both paper CRFs and EDC studies. DFdiscover is a robust clinical trial management solution that's intuitive and easy to use. It streamlines data collection from every source including paper and brings flexibility, accuracy, and speed to the daily work of collecting, verifying, and analyzing clinical data. Our strength? DFdiscover captures data from all sources, including online/offline devices! The only CDMS designed for seamless support of both paper CRFs and EDC studies
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.
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.
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.
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.
Mednet specializes in eClinical solutions designed for the global life sciences community. Beyond electronic data capture (EDC), Mednet's comprehensive platform, iMednet, is built with native applications, while enabling integrations to optimize efficiency and flexibility, delivering maximum value to clinical studies of all types and sizes. Pharmaceutical, medical device, biotechnology, and CROs have trusted Mednet for 20 years to deliver the technology and experience they need for success. A comprehensive, EDC-centric eClinical platform, delivering optimal flexibility and value for all clinical study types and phases.
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.
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.
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. Unified clinical operations suite that helps businesses plan and design protocols, create patients' consent forms, and more.
IBM Clinical Development from Watson Health is a global SaaS solution that can help the life-sciences transform clinical research and may accelerate the delivery of needed therapies to patients. With a powerful electronic data capture (EDC) system at its core, IBM Clinical Development affords clinical researchers access to hidden insights and visibility into their trial data. Scalable in both feature and function, we offer a robust suite capabilities that can be tailored to all clinical trials. IBM Clinical Development is a single, scalable cloud-based platform that lets clinical research professionals design and manage trials.
Software platform that provides EDC, patient engagement, document review, and more for clinical trial management. Software platform that provides EDC, patient engagement, document review, and more for clinical trial management.
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 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.
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
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.
User-friendly software designed for recording and analysing animal tracking within an IR actimeter. User-friendly software designed for recording and analysing animal tracking within an IR actimeter.
Catchtrial is a simple, cloud-based platform for capturing clinical trial data and images. Accessible anytime, anywhere, Catchtrial puts key information at your fingertips, resulting in shorter response times, improved compliance, and reduced costs. 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.
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.
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.
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...).
QMENTA Reader handles and streamlines the medical imaging workflow in clinical trials, ensuring quality and success all over the trial: - Create your personalized imaging workflow with our experts - Upload, anonymize and classify large amounts of data from multiple sites within seconds - Use AI & data to accurately select patients based on imaging endpoints - Create collaboration teams located in multiple spaces - Ensure quality of data and analysis anytime in the workflow with automated QC Imaging integration and management made easy with QMENTA, an advanced cloud based platform for neuroimaging.
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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.
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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.
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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.
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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.
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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.
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Comprehensive SAS based clinical data management, EDC, and clinical trials reporting system Comprehensive SAS based clinical data management, EDC, and clinical trials reporting system
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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. Electronic data capture tool that helps users create, deploy, and administer customizable intelligent data entry apps across platforms.
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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.
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A comprehensive clinical research management information system. A comprehensive clinical research management information system.
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Electronic pen and paper technology for clinical research / CRO. Electronic pen and paper technology for clinical research / CRO.
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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.
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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.
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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
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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! Clinical trial management software that helps with data management and electronic data capture using protocol tracking, and more.
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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.
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Clinical Research Organization with extensive experience in conducting Clinical Trials. Clinical Research Organization with extensive experience in conducting Clinical Trials.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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
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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.
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.
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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.
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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.
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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 CTMS on Salesforce 1 cloud platform for sponsors, clinical research organizations (CRO), hospitals, and medical centers.
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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.
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Clinical trial management solution that helps manage clinical projects, documentation & biostatistics through data coding, CRFs & more. Clinical trial management solution that helps manage clinical projects, documentation & biostatistics through data coding, CRFs & more.
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.
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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.
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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. CTMS that helps businesses recruit patients for clinical trials, assign investigators, notify about upcoming visits, and more.
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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).
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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
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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.
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Manage documents, signatures and deadlines with ease. Securely share documents anywhere, anytime. RDMS features trial and document management dashboards, electronic 21 CFR Part 11 compliant signature capture, dynamic data updates, automatic form population, deadline triggers, and change history. Flexible and scalable, VACAVA solutions are delivered via the cloud so you never have to worry about technology details. Redefine clinical trial regulatory document and TMF management with an automated, customizable 21 CFR Part 11 compliant solution.