Clinical Trial Management Software
Clinical Trial Management software helps manage all aspect of clinical trials including patient data, scheduling, reporting, analysis, and data management. This type of software can also provide tools for patient enrollment, study planning, recruitment, and decision-making in response to patient data. Clinical Trial Management software is related to Healthcare Management software, and Medical Lab software.
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- Cloud, SaaS, Web (95)
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- 21 CFR Part 11 Compliance (81)
- Document Management (72)
- Electronic Data Capture (66)
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- HIPAA Compliant (63)
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Clinical Conductor CTMS is the clinical trial management system (CTMS) designed for research sites, hospitals, AMCs, site networks, health systems & CROs. Clinical Conductor CTMS allows organizations conducting clinical research to be more efficient and profitable. Clinical Conductor CTMS is the market-leading application, making the trial process easier and allow organizations to make better business decisions and meet every challenge. Learn more about Clinical Conductor CTMS Clinical Conductor is the leading CTMS for research sites, site networks, hospitals, AMCs, CROs and health systems. Learn more about Clinical Conductor CTMS
At ClinCapture our mission is to build software that saves lives. Our technology lowers the cost of clinical trials by streamlining data capture processes while providing a platform that protects patient privacy. ClinCapture advances the evaluation and development of drugs, biologics, and devices that demonstrate promise for the diagnosis and/or treatment of a wide range of diseases or medical conditions. Request a demo today! Learn more about ClinCapture ClinCapture provides all of its customers with Private Cloud EDC, so your privacy is always protected. Request a demo today! Learn more about ClinCapture
Castor EDC is a cloud-based Electronic Data Capture platform that enables researchers to easily capture high-quality, reusable data. Features include self-service eCRF creation (form building), randomization, ePRO (patient surveys), monitoring, easy import and export of data, EHR data importer (HL7 FHIR based), audit trails, user management & much more. We are fully ISO 27001 certified, GCP & 21 CFR compliant and provide servers in the US (HIPAA compliant), UK, NL and DE. Learn more about Castor EDC The only GCP & 21 CFR compliant system that's affordable for every researcher and has all the features of expensive systems. Start now. Learn more about Castor EDC
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. Learn more about Ripple Ripple facilitates the recruitment and management of patients for clinical and translational studies. Learn more about Ripple
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. Learn more about Longboat A clinical trial management solution with a performance & engagement dashboard, patient calendars & reminders, and more. Learn more about Longboat
Ethical eAdjudication for Clinical Endpoint Adjudication is a GxP managed Software Service based on a Cloud Platform designed to support Study Leaders, Committee Members and the Q.A. Staff across the central review & adjudication of subjective endpoints. It provides the right tools/services to accomplish the Independent Review & Adjudication procedures in a timely, effective and quality controlled way. Learn more about eAdjudication Endpoint Adjudication Cloud Software Service. Designed for GxP Compliance & Effectiveness Learn more about eAdjudication
RealTime-CTMS is the leading clinical trial management system designed to increase efficiency and profitability for research sites and site networks. With fully-integrated services such as RealTime-TEXT, RealTime-PAY and the first fully-integrated eRegulatory document management system, RealTime-eDOCS, RealTime Software Solutions, LLC has the complete package of tools to help sites excel. No other CTMS can do all that RealTime does! Learn more about RealTime-CTMS Research sites & networks looking to streamline study information and company processes. We guide customers from study start to finish. Learn more about RealTime-CTMS
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. Learn more about Story Manage, distribute and optimize your content across premium publishers through 25+ social, native and content discovery partners. Learn more about Story
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. Learn more about Dacima Clinical Suite Flexible, user-friendly, web-based electronic data capture (EDC) and data management system for clinical trials and research. Learn more about Dacima Clinical Suite
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. Learn more about Clinical Trials Management ClinPlus CTMS - Designed specifically to help organizations overcome the technical challenges associated with managing clinical trials. Learn more about Clinical Trials Management
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. Learn more about Catalyst Data collection software for Applied Behavior Analysis professionals working with individuals with autism and other special needs. Learn more about Catalyst
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. Learn more about Ennov CTMS Monitor and manage clinical studies with a full web interface. Integrated to Ennov's Clinical Platform (eTMF, EDC, CDMS...). Learn more about Ennov CTMS
Data+ is a fully compliant and customizable platform for health and life science applications. Extend the capabilities of your core systems through a wide range of apps for clinical data management, drug development, lab management and more. Choose a ready-made app to configure, or create a new one from scratch using our intuitive visual designer. Empower non-technological users to create solutions on the fly and solve problems the moment they arise, alleviating the burden on IT. Learn more about Data+ Platform Data+ is a fully compliant and customizable platform for health and life-science applications. Learn more about Data+ Platform
QlikView puts information at your fingertips and frees you to make quick decisions, giving you intelligence you need to act faster. QlikView puts information at your fingertips and frees you to make quick decisions, giving you intelligence you need to act faster.
MasterControl Inc. 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.
Snappii offers many mobile apps for the Pharma-Bio Industry as a convenient and easy-to-use mobile solution that will save time and avoid unnecessary procedure, make it easy to share pharmacy information among pharmacists, eliminate mistakes caused by human factor, enable rapid and accurate data collection. App users can upload their own PDFs, edit them and share. Choose from 400+ ready-made apps or we can create the app for you. Snappii offers 400+ live business apps in 30 industries for every business. Get the mobile app for your business in days, not months.
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.
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.
Clinical Studio is a true cloud-based SaaS (Software-as-a-Service) product comprised of purpose-built software that transforms clinical research, enabling companies to efficiently complete trials on a 21 CFR Part 11 compliant system. Clinical Studio redefines clinical research software by leveraging integrated software and native mobile apps to streamline the design, deployment, and management of clinical studies. Clinical Studio facilitates research by delivering enterprise infrastructure on demand, for a flat fee.
Protocols are complex. Getting data shouldn't be. With a collaborative, drag-and-drop study designer for you and mobile-friendly forms for your sites and subjects, OpenClinica is more than just data capture. It's a better experience. The result? Higher quality data for your study, at a low cost that makes budgeting easy, too. With every deployment: secure, high-performance cloud hosting on AWS | Documented validation | FDA, EMA, GDPR and HIPAA compliance Study design, EDC, ePRO, IxRS and rich data visualizations - all on one user-friendly platform. This is your clinical data, managed.
An intuitive eSource, lab routing, and CTMS solution for research sites. Using CRIO, sites can save favorite procedures; build own source templates; capture source data quickly and accurately; mark up labs; and share visits with their monitors for review. Recruiting helps manage patients and campaigns, and enables one-click calling and texting. Finances calculates receivables and invoiceables as the visits are being completed. We are a premium service at an affordable price. An electronic source data, lab routing and CTMS system built for clinical research sites.
Target Health eSource EDC is aimed at helping organizations of all sizes with all their clinical trials software needs. As "Champions of the Paperless Clinical Trial", our patented eSource EDC software suite goes beyond direct data entry and electronic data capture (EDC), to include a clinical trial management system (CTMS), eInformed Consent, ePRO (patient reported outcomes), and includes integrated RBM reports. Backed by a CRO, we are the one-stop-shop for your EDC needs. As "Champions of the Paperless Clinical Trial", the Target Health eSource EDC software suite facilitates clinical trials of all sizes!
STARLIMS Clinical Research solution grows as your labs needs evolve, providing unrivaled flexibility and support of user-configurable workflows for a wide range of research projects, clinical trials, and laboratory processes. Feel confident in your ability to meet changing investigator needs and increasingly stringent regulations, all while providing accurate research results. Ensure labs samples are collected, handled and processed accurately with STARLIMS Clinical Research solution.
Awarded The Most Innovative Fully Comprehensive Software Solution for Clinics, Salons and Spas! Clinic Software .com gives your entire company a 360-degree view of your customers, appointments and facilitates collaboration across your organization, helping you build strong customer relationships to run and grow your business. Grow Sales. Save Time. Get Organized. Start today! Businesses of all sizes succeed with ClinicSoftware .com Advanced Features. Everything you need, all in one place. ClinicSoftware.com provides 360-degree view of your customers to help you build a strong relationship with your customers and grow!
Robust, flexible, SaaS-based Clinical Trial Management Solution (CTMS) delivered to Sponsors or CROs. Functionality includes: * Project Management * Supplies * CRF and DCF Tracking * Sponsor and Investigator Portal * Clinical Payments * Timesheet & expenses * Monitoring reports * SAE tracking * Offline Client Broad, flexible and modular CTMS solution delivered to small to mid sized sponsors or CROs.
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.
Flex Databases is a company providing e-solutions for clinical trials. We offer a unique platform which allows combining traditional features related to management of clinical trials (CTMS, EDC&IWRS) with the functionality for running internal pharma companies and CRO processes as well as a capability to manage financial data, invoicing and expenses. All modules developed by Flex Databases are validated and 21 CFR Part 11 compliant. Flex Databases is a company providing e-solutions for clinical trials.
Allegro CTMS is a cloud-based clinical trial management system that efficiently manages the operational data of clinical trials for dedicated research sites, physician practices, and community hospitals. Its superior usability, coupled with the right amount of functionality is what makes Allegro CTMS the ideal system for sites who wish to gain better visibility and control of their studies, while pursuing clinical research operations excellence. Allegro CTMS is a cloud-based clinical trial management system that manages the operational data of small to mid-sized research sites.
iMedNet eClinical delivers an innovative, cost-effective, and easy-to-use technology platform that allows non-technical research personnel to quickly build their own clinical studies...in just a matter of days, not months. And iMedNet's low Software-as-a-Service (SaaS) pricing makes it affordable for ALL study types. iMedNet eclininical has been built from the ground up based on MedNet Solution's proven, decade-long experience developing practical eClinical solutions for sponsors and CROs. An innovative, next-generation EDC/eClinical solution that allows non-technical research personnel to easily build their own studies.
Enable researchers to collect, interpret and distribute cardiac safety and clinical data accurately and efficiently. Enable researchers to collect, interpret and distribute cardiac safety and clinical data accurately and efficiently.
iDiary is ideal for a wide range studies from low to high complexity, providing sponsors with flexibility to capture patient information from early clinical development through commercialization (phase IV and health outcomes studies). Web and telephone-enabled electronic data capture of patient reported outcomes.
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.
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.
Progeny Clinical simplifies the process of managing pedigree and family history data, used by genetic counselors, clinicians and research institutions worldwide. Use online family history questionnaires to collect patient data before the clinic visit. Assess risk for hereditary cancers, order/track genetic testing and results, run custom reports, generate patient letters, integrate with your EMR and much more. Plans include pre-configured free version to fully customizable premium options. Pedigree, family history and risk assessment software used by genetic counselors, clinicians and researchers.
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.
Since 1993, Seattle-based StudyManager has been an industry-leading provider of Clinical Trial Management Software (CTMS) solutions to organizations who conduct clinical trial research. StudyManager Reveal, our Site CTMS solution, helps Sites and Hospitals organize and centralize clinical research through groundbreaking ease-of-use, power, and flexibility. Solution for research sites, universities, and hospitals streamlines clinical research, providing real-time access to key metrics.
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.
Since 1992, DataFax has been in use by CROs, Pharmaceuticals/Medical Device companies, and Global Health Organizations for the past 23 years. DataFax is an EDC system with a hybrid approach that allows our user the flexibility of designing a study/trial by EDC, paper, or both. We provide a cloud/hosted solution or clients can host the database in-house. Users will have the option of selecting from a single study fee structure or a full license, which will allow 100 plus studies. DataFax is a mature and stable Clinical Trial System, that is a true hybrid system.
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.
Cloud based platform with unified apps to optimize workflow processes, site engagement and training for global clinical trials. Cloud based platform with unified apps to optimize workflow processes, site engagement and training for global clinical trials.
From handling simple to complex GLP and non-GLP compliant laboratory environments, Xybion's enterprise solution for pre-clinical data management solution, Pristima enables a significant reduction in time to final report and study close-out through full lifecycle automation. The Pristima suite offers numerous modules, which allow you to select a targeted combination of functions to meet your specific organizational requirements and workflows. The Pristima® Suite is a fully integrated, preclinical software platform that delivers full life cycle automation for drug discovery
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.
Clinion CTMS is new age Clinical Trial Management System developed by Clinion. CTMS has all the features required for the complete management of Clinical Trial, Post Marketing Studies and Public Health Studies. Clinion CTMS is new age Clinical Trial Management System developed by Clinion.
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.
Enables clinical research professionals to collect and manage study data nearly twice as fast as the industry average. Enables clinical research professionals to collect and manage study data nearly twice as fast as the industry average.
Study management for post-approval research and registries conducted by biopharmaceutical companies, and research organizations. Study management for post-approval research and registries conducted by biopharmaceutical companies, and research organizations.
Patient Profiles is software that reads clinical trial datasets and creates individual reports (PDF, Word, HTML) for each patient. It provides both easy access to the most common tasks - reading data and creating standard profiles, for example, as well as the flexibility to adapt to the specifics of each trial and set of datasets - changing data types and formats, deriving new variables, and transposing long, skinny data structures. Perfect for clinical data managers. 30-day demo available. Clinicians can view live clinical trial patient data in real-time, in a colorful, graphical presentation on their own desktop computer.
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 i4 is a complete web-based system for creating, deploying, and administering custom data entry applications, providing data entry access anywhere you are. Entrypoint i4 architecture relies on a modular plug-in framework for maximum flexibility. The product consists of a web application for data entry and administration and three Desktop applications: Application Studio, Desktop Workstation and Desktop System Manager. All desktop applications communicate with the server. A complete system for creating, deploying, and administering custom data entry applications .
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.
A solution that enables bio-pharma and clinical research organisations to capture critical patient related details for clinical trials. A solution that enables bio-pharma and clinical research organisations to capture critical patient related details for clinical trials.
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.
Create the patient's clinical story and assign appropriate clinical terminology through computer-assisted coding. Create the patient's clinical story and assign appropriate clinical terminology through computer-assisted coding.
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.
Software that provides document routing, submission tracking, protocol deviation review, and strict data access control, Software that provides document routing, submission tracking, protocol deviation review, and strict data access control,
Clinical data management solution with data queries generation, audit trails, electronic signatures, and data reconciliation tools. Clinical data management solution with data queries generation, audit trails, electronic signatures, and data reconciliation tools.
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.
Comprehensive system that allows to securely keep specimen data from multiple studies and supports various data mining tools. Comprehensive system that allows to securely keep specimen data from multiple studies and supports various data mining tools.
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.
BizNET, A clinical trials management software offers an integrated suite of software products for CROs, Pharmaceutical, Biotech Industries and Medical device industries. Our solution blends various integrated modules that prominently support clinical trial activities like EDC/DDC data collection, IWRS & drug randomization management, CDISC SDTM. It is a validated software, compliant with 21 CFR part 11 and GCP guidelines which provide a transparent and smooth process to regulatory For clinical research projects - project management, feasibility assessment, enrollment, data capture, compilation, archiving.
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.
Cloudbyz offers Clinical Trial Management on Salesforce 1 cloud platform for sponsors, clinical research organizations (CRO), hospitals and medical centers. CTM on Salesforce 1 cloud platform for sponsors, clinical research organizations (CRO), hospitals and medical centers.
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.
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.
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)..
Our CTMS software is easy to operate, thereby saving you time and costs. The software adapts to your requirements, and not the other way around. BSI CTMS seamlessly integrates into your system environment, interfacing all necessary peripheral systems as a cloud or on-premise solution. This makes BSI CTMS the central hub for all aspects of your clinical trials. BSI CTMS covers all aspects of clinical trial management. It is the most intuitive and flexible system on the market. Test us out.
Are you tired of using a CTMS that is overcomplicated, has a poor user interface and costs way too much money? At Intrinsic, we solved these problems by developing an easy to use practical CTMS that is cloud based. Intrinsic has 4 key clinical software productsCTMS, eTMF, study portals, and investigator portalsthat help pharma companies more easily manage their trials and CROs. Each module can be purchased separately, or users can enjoy the benefits of an integrated suite of clinical systems. Are you tired of using a CTMS that is overcomplicated, has a poor interface and costs too much? Contact us to learn more.
An interactive environment for multimodal biosignal data processing and analysis in the fields of clinical research and life sciences An interactive environment for multimodal biosignal data processing and analysis in the fields of clinical research and life sciences
Prelude Dynamics helps companies focusing in the Pharmaceutical, Biotechnology, Medical Device, and Academia focusing on Human & Animal Health industries to streamline and accelerate their clinical development pipelines with a cost-effective and flexible study EDC/CTMS solutions. [8:55] VISION simplifies, standardizes, and automates the collection and cleaning of data for clinical trials, in near real- Provides integrated solutions to automate Electronic Data Capture, Data Management, and Project Management needs.
KLINDAT is a next-generation electronic Case Report Form (eCRF) for the pharmaceutical, biotech & medical device industries. KLINDAT is a next-generation electronic Case Report Form (eCRF) for the pharmaceutical, biotech & medical device industries.
An advanced clinical trial management system (CTMS) allowing multiple studies across different sites to be supported. An advanced clinical trial management system (CTMS) allowing multiple studies across different sites to be supported.
Software made with an objective. Using technology we wanted to provide better care for patients and increase the revenue of the service providers. We started looking for products do just that. Since we couldn't find one, we made SimplexHIMES. SimplexHIMES is a cloud-enabled Clinic management software that is highly configurable to suit any type of customer. The regional plugin provides local requirements and regulatory needs of any region. Enterprise level product that can scale up on demand. Practice management software that is highly configurable for any customer requirements.
Comprehensive eSource system for all the source data for clinical trials with source, regulation, and drug accountability. Comprehensive eSource system for all the source data for clinical trials with source, regulation, and drug accountability.
Configurable CTMS that helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases. Configurable CTMS that helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases.
The comprehensive AssessRx solution is designed to assess a clinicians ability to consistently and safely apply clinical knowledge, skills, and judgment through the use of multiple valid and reliable assessments. This solution helps organizations quickly identify a clinician's ability to recognize and respond to urgent patient situations as well as effectively communicate with others within the healthcare team. HealthStream Competency Center is competency-driven, healthcare specific, and a HealthStream-integrated competency management system.
Nucleus is a platform that combines all aspects of clinical development into one convenient location, allowing you and your team to manage documents, communicate with one another and access your clinical information from the same application. Nucleus provides a cost-effective hub for clinical information (documents, communication, and technologies) to enhance collaboration.
Teamscope is an Electronic Data Capture (EDC) platform available on iOS and Android for clinical and field research. Build your studies using our point&click interface, generate real-time reports and keep your data secure and protected at all moments. Use Teamscope to collect data for clinical studies, even when you are offline or in remote areas.
An advanced electronic data capturing and clinical trial solution built specifically for the oncology department. An advanced electronic data capturing and clinical trial solution built specifically for the oncology department.
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.
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.
Cloud-based clinical trial data management solution that comes with integrated randomization models, built-in QA control, data change tracking, and graphical tools. Cloud-based clinical trial data management solution that comes with randomization models, built-in QA control, and graphical tools.