Pharmaceutical companies use clinical trial management systems to manage clinical trials as part of their pharmaceutical and biotechnology research activities. Medical research institutes and research centers managed by hospitals may also use clinical trial management software. These systems help healthcare companies improve the quality of their products, optimize their times to market, and ensure compliance with industry specific regulations. This type of software is used by researchers to define, implement, and track results of clinical trials. Administrative personnel of clinical trials also use this type of application to find and schedule participants, and track their involvement in the trials.
Clinical trial management software may require integration with other healthcare solutions such as laboratory information management systems (LIMSs), hospital management systems, or analytics and data management solutions.
To qualify for inclusion in the Clinical Trial Management category, a product must:
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The MasterControl Clinical Suite, a clinical management software system, is designed to manage all of the documents, tasks, processes, relationships, audits, and training that must be administered and controlled throughout the life of a clinical trial.
Academic medical centers, cancer centers, and health care systems manage hundreds of protocols at once in an environment where there are many other, often competing, concerns ranging from limited resources to meeting ever-changing regulatory requirements. Furthermore, gaining visibility into operations and maintaining effective communication across research groups can pose significant challenges. The OnCore® Enterprise Research system, the leading enterprise-class clinical research management system, has a long history of successfully addressing the broad spectrum of challenges. For over a dozen years, it has supported operations at leading research organizations across the country. What is the OnCore Enterprise Research system? The system incorporates essential modules for managing all protocols across the enterprise. The modules include clinical research management, billing compliance, electronic data capture, biospecimen management, patient registries, and integrations.
Used by more organizations around the world than any other CTMS, Clinical Conductor standardizes and simplifies complex processes for research organizations managing and conducting clinical trials. Created by Bio-Optronics, it is the leading CTMS for managing research and executing collaboratively across multiple clinical trials and sites. The role-based system provides the comprehensive features and functionality needed to recruit effectively, improve patient visit satisfaction, optimize billing, maintain research compliance, extract actionable business insight and maximize profitability. With over two thousand deployments of Clinical Conductor so far, Bio-Optronics has established fail-safe deployment process that gets organizations up and running quickly and effectively, with 24x7 support services and unlimited ongoing web-based training.
With a robust electronic data capture (EDC) system at its core, IBM® Clinical Development is an all-in-one, cloud-based data management platform that lets you design and manage clinical trials with more control, convenience and confidence than ever before. IBM Clinical Development offers a host of powerful tools—from randomization, dispensing and reporting to endpoint adjudication and ePRO (electronic patient reported outcomes)—that help you launch and complete studies more efficiently and bring needed products to patients sooner. Used by clinical professionals worldwide, the platform lets you capture, manage, analyze and report study data across therapeutic areas, trial types and time zones. A SaaS solution, IBM Clinical Development requires no special infrastructure or prior programming experience to use. Designed to be intuitive and easy to navigate, you access all study data and platform functions through a centralized, password-protected web interface.
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.
Clinion™ is a 21 CFR Part 11 validated Intuitive Electronic Data Capture (Intuitive EDC) and Clinical Data Management (Paper Study) platform.Clinion™ is focused on reducing the new product time-to-market for Pharmaceutical, Biotech and Medical Device Organizations by providing a highly configurable and user-friendly Clinical Trials Application. Clinion™ is easy to use and configure and does not require any hardware and software requirements from the client.It is available online and can be securely accessed from anywhere by authorized users.
Clinical Trial Management built 100% native on Salesforce platform and available on AppExchange. https://appexchange.salesforce.com/listingDetail?listingId=a0N3000000B56ueEAB Capabilities include: Clinical Program Management Global Trials Management Investigator Management Protocols Management Clinical Sites Management Sites Evaluation and Selection Subjects Enrollment and Management Template Driven Site Plan and Activity Management Site Calendar View Case Report Form (CRF) Adverse Events Management Payments Clinical Supply Management Real-time Reports and Dashboards
Data+ is a revolutionary data management solution for clinical research. We deliver an all-in-one solution for research organizations - connecting the organization, researchers, and patients together. Our focus is on insights - to improve care, team and time management, and patient engagement as well as compliance using informative feedback.
DATATRAK provides industry-leading digital software for clinical trials. Responsive to the needs of each unique trial, we simplify the management of data for modern trials. Clients can make informed decisions faster with our standard and ad-hoc reporting capabilities, right through the interface, all with real-time data. We offer EDC, RTSM, a transformational CTMS solution, Trial Design, and Training, leveraging a single truth to eliminate redundant processes. See how DATATRAK can simplify the management of data for clinical trials.
DSG Designer lets the user be the creator with complete control of workflow to help streamline trial execution. DSG Designer offers the design flexibility to mix and match your eCRFs in both a Table Layout and Free Form Layout together within the same study. DSG’s unparalleled support services and hands-on training ensure that you build studies end-to-end. We help you create reusable templates and eCRFs that can lower your cost to deliver a completed study for regulatory approval. Accelerate the design process with our complete and exhaustive library of pre-defined edits based on years of full service edc experience.
eAdjudication ® supports Endpoint Adjudication with a user-friendly Cloud Software exclusively designed to support Study Leaders, Committee Members and the Q.A. Staff across the central review & assessment of subjective or image based endpoints. eAdjudication software is provided as an all-inclusive Cloud Service package bundled together with hosting, technical management, validation, training & support: > unlimited users Licenses of the software; > configuration to map the Adjudication Charter and Workflows; > ISO 27001 cloud hosting for system and database; > server, database and study data complete technical management; > standard users support / integrated online Helpdesk; > standard users training / testing in a Clone "Stage" environment; > GxP validation package documentation & support.
DSG’s award-winning eCaseLink software is the most advanced EDC solution in the industry. eCaseLink 8.2 is a truly integrated eClinical solution that seamlessly combines CTMS, EDC, IWRS and Safety into a single system, cutting costs and giving you control over your entire study. Unlike other systems that attempt to force completely unrelated systems to work together, eCaseLink was developed from the ground up as a truly integrated system whose parts work effectively as a whole. eCaseLink helps you to see everything that’s happening with your study in real time, at all times. This unmatched level of control helps you to make mid-study changes, contain costs, improve safety and increase ROI.
eCaseLink.Me provides a flexible approach to patient-reported data capture. eCaseLink.Me can be used alone or in combination with eCaseLink EDC software for reporting and data analysis. Designed with the patient in mind, eCaseLink.Me allows patients to personalize and change the appearance of the application to better suit preferences. It works on any browser or web-enabled device, so that patients may enter data conveniently from any wifi-enabled location – no need for unfamiliar devices.
Our CTMS consists of a number of modules (CRA Activity Management, Subject Tracking & Invoicing, Investigator and Site Management), which can be used together, separately or with other modules on our platform. You may choose certain options now and increase your use of CTMS anytime in the future.
Prism is a fully integrated clinical trial management and EDC product that provides both standard data management functionality and value-added tools for clinical trial management. Prism combines ease-of-use with innovative features to provide a fresh solution for the collection and management of clinical trial data.
Whether hosted in our compliant cloud or on-premises, we have extensive experience in the implementation and integration of the most widely used and highly sought-after clinical and pharmacovigilance software applications. In addition to helping you select, implement, integrate, use, and maintain a variety of systems, we can efficiently and cost-effectively assist with software licensing, migrations, and upgrades.
NEW--Site Monitoring Visit Report process added to Perform --NEW Perform is a unified Clinical Operations platform for CTMS, EDC, Document Control, Contact Management, and Query Resolution that is GREAT for SMALL to MID-SIZE SPONSORS or CROs. Rapid set-up and Role-based training gets small teams running quickly. Our PLAN > DO > VIEW Methodology enables actual USERS to benefit from Perform as well as MANAGEMENT. Subscription Pricing by Function. Real-time status/progress report.
SEND Savante, is a comprehensive solution for data aggregation, query, analysis, and reporting of pre-clinical drug discovery and drug development data. Integrated with the industry-standard Pristima pre-clinical software suite, it allows organizations to build a consolidated data warehouse containing study data coalesced from multiple sources, based on CDISC-SEND standards.
SimpleTrials is a Clinical Trial Management System for Sponsors, CROs and Sites. SimpleCTMS was designed and developed to offer the benefits of a CTMS (Clinical Trial Management System) without the extensive upfront financial and resource commitments associated with traditional enterprise systems or the inherent inefficiencies of worksheet trackers.
StudyManager Reveal is an industry-leading provider of Clinical Trial Management Software (CTMS) solutions to organizations who conduct clinical trial research. StudyManager Reveal helps Sites and Hospitals organize and centralize clinical research through groundbreaking ease-of-use, power, and flexibility.
SyMetric C6 is a platform that hosts our IWRS and EDC solutions within a single ecosystem; combining our Sites and Patients Handling, Drug Logistics Handling, Case Form Management and Reporting Modules seamlessly. Its' robust framework and integrated platform makes it cost effective, simple to use and efficient in managing data.
TrialStat enables you to use one system for all clinical phases including, from build your own EDC for Phase 1; to advanced EDC, CTMS, and Portal functionality for Phase 2 and 3; to flexible electronic patient access for Late Phase.