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Castor EDC is een cloudgebaseerd platform voor elektronische gegevensvastlegging waarmee onderzoekers gemakkelijk hoogwaardige, herbruikbare gegevens kunnen vastleggen. Functies omvatten self-service eCRF-creatie (formulieropbouw), randomisatie, ePRO (patiënt-enquêtes), monitoring, eenvoudige import en export van gegevens, EHR-gegevensimporteur (gebaseerd op HL7 FHIR), audittrails, gebruikersbeheer en nog veel meer. Castor EDC is volledig ISO 27001-gecertificeerd, voldoet aan de vereisten van GCP en 21 CFR en biedt servers in de VS (compatibel met HIPAA), VK, NL, DE. Meer informatie over Castor EDC Het enige systeem dat voldoet aan de voorschriften van GCP en 21 CFR, dat betaalbaar is voor elke onderzoeker en toch beschikt over alle functies van dure systemen. Begin direct. Meer informatie over Castor EDC
Clinical Conductor CTMS is het beheersysteem voor klinische proeven (CTMS) dat is ontworpen voor onderzoekslocaties, ziekenhuizen, AMC's, sitenetwerken, zorginstanties en CRO's. Met Clinical Conductor CTMS worden organisaties die klinisch onderzoek uitvoeren efficiënter en winstgevender. Clinical Conductor CTMS is een toonaangevende toepassing waarmee het proefproces eenvoudiger wordt en organisaties betere zakelijke beslissingen kunnen nemen en elke uitdaging aankunnen. Meer informatie over Clinical Conductor CTMS Clinical Conductor is het leidende CTMS voor onderzoekslocaties, sitenetwerken, ziekenhuizen, AMC's, CRO's en zorginstanties. Meer informatie over Clinical Conductor CTMS
Protocollen zijn complex. Gegevensverzameling zou dat niet moeten zijn. Met een op samenwerking gerichte onderzoeksontwerpfunctie met slepen en neerzetten voor jou, en mobielvriendelijke formulieren voor je vestigingen en proefpersonen, biedt OpenClinica meer dan alleen maar gegevensverzameling. Het biedt een betere ervaring. Het resultaat? Gegevens van hogere kwaliteit voor je studie, tegen lage kosten die budgettering ook nog eens eenvoudig maken. Met elke implementatie: veilige, krachtige cloudhosting op AWS | Gedocumenteerde validatie | Conformiteit met FDA, EMA, AVG en HIPAA Meer informatie over OpenClinica Studieontwerp, EDC, ePRO, IxRS en rijke datavisualisaties - allemaal op één gebruiksvriendelijk platform. Dit zijn je klinische gegevens, maar dan beheerd. Meer informatie over OpenClinica
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. Meer informatie over EDGE A global, innovative, cloud-based clinical trial management system providing faster access to real-time data. Meer informatie over EDGE
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Longboats clinical trial support platform creates an environment where protocol compliance is instinctive, teams are virtually guided at all times and all stakeholders have the knowledge and resources they need to conduct the trial. Clinical operations, monitors, site staff, and patients access the one integrated and consistent support platform. Depending on the users role in the study the interface, and support provided, adjusts to meet their specific needs. Meer informatie over Longboat A clinical trial management solution with a performance & engagement dashboard, patient calendars & reminders, and more. Meer informatie over Longboat
Smartsheet, een online platform voor het uitvoeren van werkzaamheden, stelt farmaceutische bedrijven en klinische onderzoeksorganisaties in staat om klinische tests en proeven te volgen, te beheren en erover te rapporteren. Door de vertrouwde spreadsheetindeling stelt Smartsheet teams in staat om moeiteloos aan de slag te gaan en effectief samen te werken. Je kunt persoonlijke gezondheidsgegevens (PHI) veilig delen, opslaan en bekijken terwijl je voldoet aan de wettelijke vereisten van HIPAA. Bovendien hoef je met realtime dashboards minder tijd aan het proces te besteden en kun je meer tijd besteden aan het leveren van resultaten. Meer informatie over Smartsheet Smartsheet is een online platform voor de uitvoering van werk dat organisaties van elke omvang in staat stelt om werk te plannen, te beheren, te automatiseren en erover te rapporteren. Meer informatie over Smartsheet
Caspio is een toonaangevend platform met weinig code voor het bouwen van toepassingen voor het beheer van klinische onderzoeken zonder te hoeven programmeren. Het alles-in-één platform is door Forrester Research benoemd als Leider en biedt alles wat je nodig hebt om bedrijfsactiviteiten en workflows digitaal te transformeren. Het omvat een geïntegreerde clouddatabase, een bouwer voor visuele applicaties, professionele beveiliging, naleving van regelgeving en een schaalbare wereldwijde infrastructuur. Caspio wordt wereldwijd vertrouwd door meer dan 12.000 bedrijven. Probeer het GRATIS uit. Meer informatie over Caspio Caspio is een toonaangevend platform met weinig code voor het bouwen van toepassingen voor het beheer van klinische onderzoeken zonder te hoeven programmeren. Meer informatie over Caspio
Research Manager faciliteert degenen die zich bezighouden met onderzoek op het gebied van biowetenschappen met een online onderzoeksplatform voor alles wat met onderzoek en registraties te maken heeft. Het platform fungeert als een centraal punt waar onderzoekers, onderzoekscoördinatoren en ethische commissies toegang hebben tot diensten en informatie, waardoor ze gegevens verder kunnen ontwikkelen en verbeteren. Research Manager biedt ook expertise op het gebied van gegevensverzameling, validatie en verrijking. Meer informatie over Research Manager Waarde toevoegen aan data. Research Manager biedt een onderzoeksplatform waar procesbeheer en gegevensverzameling zijn geïntegreerd. Meer informatie over Research Manager
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! Meer informatie over DFdiscover The only CDMS designed for seamless support of both paper CRFs and EDC studies Meer informatie over DFdiscover
Cloud Platform is een set van modulaire cloudgebaseerde diensten waarmee je alles kunt maken, van eenvoudige websites tot complexe toepassingen. Cloud Platform is een set van modulaire cloudgebaseerde diensten waarmee je alles kunt maken, van eenvoudige websites tot complexe toepassingen.
Snappii biedt veel mobiele apps voor de Pharma-Bio-industrie als een handige en gemakkelijk te gebruiken mobiele oplossing die tijd bespaart en onnodige procedures voorkomt, die het gemakkelijk maakt om apotheekinformatie onder apothekers te delen, fouten door menselijke factoren elimineert, snel in te schakelen is en nauwkeurig gegevens verzamelt. App-gebruikers kunnen hun eigen pdf's uploaden, bewerken en delen. Kies uit meer dan 400 kant-en-klare apps of er kan een app voor je worden ontworpen. Snappii is een toonaangevend bedrijf voor mobiele apps en formulierenapps. Ongeveer 500.000 mensen gebruiken Snappii Business-apps in 30+ sectoren.
Medrio's suite of cloud-hosted eClinical platforms empower researchers to accelerate their clinical trials, reduce study costs, and bring life-saving products to market. Our EDC, eSource, eConsent, and ePRO tools require no programming to set up, and deliver next-level efficiencies in study build, mid-study changes, monitoring, data quality, and more. Medrio was tailor-made for early phase pharma, medical device, and diagnostics studies. Book a demo today to see the platform for yourself. Medrio provides fast and easy-to-use eClinical solutions with no programming required.
RealTime Software Solution is een SAAS-gebaseerd systeem voor het beheer van klinische tests voor sites, sponsors en CRO's. RealTime is ook de enige CTMS-leverancier die een compleet pakket oplossingen kan bieden in een naadloos platform, het systeem voor het beheer van site-activiteiten. SOMS omvat de CTMS, SitePAY, TEXT, eDOCS en eSOURCE die toegankelijk zijn via een gebruiksvriendelijke MobileAPP. RealTime biedt ook een oplossing op ondernemingsniveau voor grote sites en sitenetwerken. Onderzoekssites en netwerken die onderzoeksinformatie en bedrijfsprocessen willen stroomlijnen. Klanten worden van het begin van het onderzoek tot het eind begeleid.
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 is een waar cloudgebaseerd SaaS-product (Software-as-a-Service) dat bestaat uit speciaal ontwikkelde software die klinisch onderzoek transformeert, waardoor bedrijven op een efficiënte manier tests kunnen voltooien op een 21 CFR Part 11-conform systeem. Clinical Studio geeft een nieuwe definitie aan klinische onderzoekssoftware door gebruik te maken van geïntegreerde software en native mobiele apps die het ontwerp, de implementatie en het beheer van klinische onderzoeken stroomlijnen. Clinical Studio vergemakkelijkt onderzoek door on-demand infrastructuur voor grote ondernemingen te leveren, tegen een vast bedrag.
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.
Klinieken van elke omvang behalen succes met ClinicSoftware.com. Ben je op zoek naar een alternatief voor CRM-software? Twee stappen vooruit. Maak het runnen van je bedrijf slimmer, beter, sneller. Onmiddellijk. ClinicSoftware.com is een volledig pakket van tools in de cloud die zijn gecreëerd om ondernemingen en op afspraak gebaseerde bedrijven uit elke sector en van elke omvang, zoals klinieken, spa's en salons, te helpen hun omzet te vergroten, tijd te besparen en beter georganiseerd te zijn. ClinicSoftware.com is bekroond als de meest innovatieve software in de sector en wordt aanbevolen door 98% van de klanten. Ben je op zoek naar een alternatief voor CRM-software? Twee stappen vooruit. Maak het runnen van je bedrijf slimmer, beter, sneller. Onmiddellijk.
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 is een cloudgebaseerde oplossing voor elektronische gegevensvastlegging waarmee onderzoekers snel nauwkeurig en betrouwbare gegevens kunnen verzamelen voor analyse. MACRO voldoet aan ethische en wetenschappelijke kwaliteitsnormen voor het ontwerpen, uitvoeren, registreren en rapporteren van klinische proeven met menselijke proefpersonen. Tot de functies behoren self-service eCRF-creatie (formulieren ontwerpen), eenvoudige export van gegevens, controlesporen, gebruikersbeheer en veel meer. ISO 27001 gecertificeerd, conform GCP en 21 CFR, voldoet aan de WCAG2-AA-toegankelijkheidsnormen. Elektronische gegevensvastlegging van Elsevier: ondersteunt klinisch onderzoek.
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+ is een volledig compatibel en aanpasbaar platform voor toepassingen in de gezondheidszorg en levenswetenschappen. Breid de mogelijkheden van je kernsystemen uit met een breed scala aan apps voor klinisch gegevensbeheer, ontwikkeling van geneesmiddelen, laboratoriumbeheer en meer. Kies een kant-en-klare app om te configureren of creëer een geheel nieuwe app met deze intuïtieve visuele ontwerper. Stel niet-technologische gebruikers in staat om oplossingen te vinden en problemen op te lossen zodra ze zich voordoen, waardoor de lasten voor de IT-afdeling worden verlicht. Data+ is een volledig compatibel en aanpasbaar platform voor toepassingen in de gezondheidszorg en levenswetenschappen.
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.
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.
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.