Software per studi clinici
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- Cloud, SaaS, Web (112)
- Dispositivi mobili - Android nativo (21)
- Dispositivi mobili - iOS nativo (22)
- Installazione eseguita - Mac (10)
- Installazione eseguita - Windows (30)
- Acquisizione elettronica dei dati (74)
- Banca dati dei pazienti (67)
- Conforme alla legge HIPAA (69)
- Conformità 21 CFR Part 11 (84)
- Gestione della selezione del personale (44)
- Gestione delle iscrizioni (65)
- Gestione di documenti (82)
- Monitoraggio (82)
- Pianificazione degli studi (64)
- Programmazione (68)
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
Pristima è una soluzione aziendale completamente integrata per la gestione dei dati preclinici, che offre automazione durante l'intero ciclo di vita e supporto per la gestione degli studi di ricerca su farmacologia e sicurezza dei farmaci, la gestione dei terrari e le cure veterinarie. Dalle colture e dagli ordini fino al processo di presentazione dello studio, Pristima Suite gestisce la pianificazione e la registrazione dei dati, controlla le modifiche autorizzate e assembla i dati per la presentazione alle agenzie di regolamentazione. Ulteriori informazioni su Pristima Pristima® Suite è un software preclinico completamente integrato, che offre automazione durante l'intero ciclo di vita e supporto per ricerca e sviluppo preclinici. Ulteriori informazioni su Pristima
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
Ethical eAdjudication for Clinical Endpoint Adjudication è un servizio software gestito da GxP e basato su una piattaforma cloud, progettato per supportare i responsabili degli studi, i membri dei comitati e il personale addetto al controllo qualità durante l'intero processo di revisione e aggiudicazione centrale degli endpoint soggettivi. Fornisce gli strumenti/i servizi giusti per completare procedure di revisione e aggiudicazione indipendenti in modo tempestivo, efficace e con qualità controllata. Ulteriori informazioni su eAdjudication Servizio software nel cloud per l'aggiudicazione degli endpoint. Progettato per la conformità e l'efficacia GxP Ulteriori informazioni su eAdjudication
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
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. Ulteriori informazioni su Clinical Studio Clinical Studio facilita la ricerca fornendo un'infrastruttura aziendale on-demand a pagamento. Ulteriori informazioni su Clinical Studio
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. Ulteriori informazioni su Data+ Platform Data+ è una piattaforma completamente conforme e personalizzabile per applicazioni dedicate a salute e scienze naturali. Ulteriori informazioni su Data+ Platform
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 is a leading Mobile Apps and form apps company. About 500,000 people use Snappii Business Apps in 30+ Industries.
RealTime Software Solution is a global leader in SAAS-based Clinical Trials Management Systems for Sites, Sponsors, and CROs. RealTime is also the only CTMS vendor that can offer a complete suite of solutions into a seamless platform, Site Operations Management System (SOMS). SOMS includes the industry-leading CTMS, SitePAY, TEXT, eDOCS, and eSOURCE which is accessible through an easy-to-use MobileAPP. RealTime also offers an enterprise-level solution for large sites and site-networks. Research sites & networks looking to streamline study information and company processes. We guide customers from study start to finish.
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.
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.
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.
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.
The EDGE system, developed by the Clinical Informatics Research Unit at the University of Southampton, is already embedded across 80% of the NHS within the UK and is quickly becoming a front runner for clinical trial management systems internationally. EDGE provides users with faster access to real-time data and complete study oversight from start to finish. Email [email protected] for more information or to request a free demo. An innovative cloud-based clinical trial management system giving a real-time view of clinical research activity.
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.
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.
VISION EDC is the industry leader in late phase studies. Our combination of software and services enables CROs and Sponsors to craft a database that fits their unique needs. Manage mid-study updates with ease. Build your own studies or leverage our team of certified data managers to design and build your eCRFs for you. Features include: patient mobile app for direct data entry, integrated Randomization, direct lab uploads, site invoicing, automatic dictionary coding and much more VISION EDC is the industry leader in late phase studies for human and animal trials.
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.
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.
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.
Teamscope is a mobile data collection app for clinical and field research. Create powerful mobile forms, collect data offline and visualize it with a few clicks. 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.
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.
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.
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.
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.
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.
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.
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
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.
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.
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.
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.
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.
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...).
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
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.
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.
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.
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.
Helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development. Helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development.
Cloud-based solution that allows life science companies to manage clinical trial process providing clinical trial activities planning, tracking and control. Cloud-based solution with clinical trial activities planning, tracking and control for life science organizations.
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 .
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.
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.
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
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.
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.
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.
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.
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.
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.
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.
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.
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
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.
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.
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.
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.
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.
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.
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.
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).
Help your Clinical Operations team continuously improve speed, efficiency and data quality across your portfolio of clinical trials Help your Clinical Operations team continuously improve speed, efficiency and data quality across your portfolio of clinical trials
A disruptive big data SaaS platform, that accelerates new drug launches,lowers clinical trial costs, and enables RBM. A disruptive big data SaaS platform, that accelerates new drug launches,lowers clinical trial costs, and enables RBM.
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.
The "Astracore Clinical Trials System" is a cloud-based solution for your CRF or eCRF needs. Very quick to set up for your specific needs with many features, and readily customizable for any unique or specific features. Able to store supporting documents, images, audio and video. Can upload existing CRFs or data collection templates or start from scratch. Free and non-obligation custom configuration and trial available - just contact us for details. Cloud based computer system for entering, storing, extracting, analysing and reporting of Clinical Trials Data (eCRF)..
Whether as a sponsor, CRO or SMO BSI life sciences software covers your specific processes and features. Plan and manage all aspects of your clinical trials like patient engagement, clinical trial management (CTMS), trial master file (eTMF), study start-up, and trial supply management (RTSM) with the clinical software solutions from BSI. Regardless of whether you need a completely new system, or would like to improve your existing CTMS, you are in the right place with BSI. BSI CTMS covers all aspects of clinical trial management. It is the most intuitive and flexible system on the market. Test us out.