Alternatives to OneStudyTeam
Compare OneStudyTeam alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to OneStudyTeam in 2026. Compare features, ratings, user reviews, pricing, and more from OneStudyTeam competitors and alternatives in order to make an informed decision for your business.
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Medrio
Medrio
Medrio is on a mission to ease complexity in today’s hybrid, decentralized, and site-based clinical trials by delivering a flexible suite of eClinical technologies and services, including EDC, eCOA, ePRO, eConsent, Direct Data Capture, and Randomization and Trial Supply Management (RTSM). Trusted by CROs, sponsors, and sites across all therapeutic areas and trial phases from study startup and feasibility to post-market approval, we are industry-recognized for delivering eClinical software with intuitive interfaces and time-saving “drag and drop” configurations as well as high-touch customer engagement, onboarding, and support services. Medrio’s innovative software, as well as the robust and flexible training and support resources we provide our customers, have earned us a 98% customer satisfaction rating. -
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Antidote
Antidote
Antidote is a clinical trial recruitment platform that accelerates medical research by uniting patients and sponsors through precision recruitment services and an intuitive match search engine. By tackling the fact that over 80% of trials are delayed for want of participants, Antidote offers sponsors a vendor-agnostic, centralized dashboard that standardizes referrals from any partner, automates due diligence outreach and owner letters, tracks real-time enrollment and ROI metrics, and delivers actionable site and candidate insights via hourly-updated analytics. For patients, Antidote’s smart match engine transforms complex inclusion and exclusion criteria into simple, guided question-and-answer flows, then presents up-to-date clinical trial listings and personalized alerts when new matches appear. It supports bulk or single-record imports with automated validations and provides multilingual, mobile-friendly interfaces. -
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Cloudbyz CTMS
Cloudbyz
Cloudbyz CTMS is a cloud-based trial management platform natively built on Salesforce Cloud. It is aimed at sponsors, clinical research organizations (CRO), and clinical sites for managing end-to-end clinical trial operations. Designed for clinical research, it expedites implementation and drives user adoption. Cloudbyz CTMS comes with an intuitive, straightforward design that allows for quick deployment. Boasting a rich set of features, Cloudbyz CTMS makes it easy for users to manage all aspects of clinical trials, including sites, enrolment, documents, events, milestones, site visit reports, finances, inventory, etc. Cloudbyz provides end-to-end management of the clinical trial lifecycle, including study setup, site management, study projections, monitoring, and financial management. With Cloudbyz, you can optimize your study planning, accelerate patient recruitment, and increase trial quality, while reducing costs and minimizing risk. -
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Jeeva eClinical Cloud
Jeeva Informatics Solutions
Jeeva's patent-pending modular solution is designed from the ground up on the most powerful cloud platform with one login from any browser-enabled mobile device for remote patient screening, education, enrollment, electronic informed consent, bi-directional communications via video calling, telemedicine, SMS, email, and evidence generation including electronic patient-reported outcomes and clinical outcomes assessments, with a modern user experience. Delays in patient recruitment & retention are keeping them up at night. Generating enough evidence of safety and efficacy of investigational new medicines is critical to get timely approval from regulatory agencies. Whether you are a patient group setting up a registry or natural history study, or a biopharma sponsor of a clinical trial, or a long-term follow-up study for gene therapy, Jeeva can save you time, and money while improving user experience for study team and trial participants.Starting Price: $100/mo/user -
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Leapcure
Leapcure
Leapcure is a leading patient recruitment and engagement platform that connects clinical trial sponsors with eligible patients. Utilizing advanced technology and strategies, we enhance trial participation and improve patient outcomes. Our platform streamlines the recruitment process, ensuring that trials are populated with suitable candidates quickly and efficiently. Leapcure is dedicated to advancing medical research by making clinical trials more accessible and effective. We work closely with sponsors and patients to facilitate smooth and successful trial experiences, ultimately contributing to the development of new treatments and therapies. -
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Rave CTMS
Dassault Systèmes
Study teams are increasingly being challenged to do more with fewer resources. Delays caused by disconnected systems, manual data re-entry, redundant workflows, and information silos can seriously affect a trial’s progress. You need a clinical trial management system that unifies and streamlines workflows while still maintaining full visibility, and Medidata has the solution. Rave CTMS is the only data-driven solution for faster, smarter, end-to-end trial management. As an integral part of the Medidata Rave Clinical CloudTM, Medidata provides all of the elements you expect from an industry-leading CTMS and more. Rave CTMS provides your study teams with the ability to plan and manage all of your clinical trials in a consistent and harmonized manner that standardizes activity planning and management at the study, country, and site level. Activities include study/site team creation and activation, patient enrollment and milestone tracking, site monitoring, and issue management. -
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Clinion CTMS
Clinion
Most Easy-to-Use Clinical Trial Management System (CTMS) 𝐂𝐥𝐢𝐧𝐢𝐨𝐧 𝐂𝐓𝐌𝐒 integrates seamlessly with Clinion EDC and Clinion RTSM to provide detailed and faster access to the entire trial process to address all aspects of Clinical trial management from a single platform: investigator sites, patients enrollment, SAEs, deviations, inclusions, visit scheduling, IP management, milestones, finances, custom reports, and on-demand analytics enables you to improve quality, control risk, and reduce costs. Our Clinical Trial Management System allows CROs and Sponsors to monitor the trial progress actively with its advanced dashboard and alert notification system. So you’ll never miss a deadline again! What can you expect? Comprehensive CTMS Software Single Source for your entire trial data On-demand Analytics for Risk-Based Management of Clinical Trials Fully Integrated with Clinion EDC and Clinion RTSM 100% web-based and hosted securely on the cloud 21 CFR Part 11 & GD -
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ClinEdge
ClinEdge
ClinEdge is transforming the clinical trial industry by providing a comprehensive suite of services tailored for Sponsors, CROs and Sites. We creatively and collaboratively solve problems for our clients because we understand the challenges and barriers they face. ClinEdge is dedicated to improving overall trial success through every stage of every study by providing Site and Patient Access to Sponsors/CROs and enhanced Trial Solutions to Site partners. With over a decade of expertise and a deep understanding of our clients and the challenges they face, ClinEdge is focused on transforming and revolutionizing study conduct. -
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Ennov CTMS
Ennov
Ennov CTMS facilitates the end-to-end management of clinical trials. The software allows sponsors to be more efficient, to make better decisions, to ensure compliance, to select investigators well, to monitor patient recruitment and to manage finances. Ennov CTMS includes comprehensive directories to manage site personnel (investigators, sub-investigators, study coordinators, pharmacists) and organizations (hospitals, competent authorities, CROs, suppliers). Ennov CTMS provides functions for tracking patients, patient visits, EDC data, activities, queries, deviations, adverse events, drug supply, monitoring visits and finances. A full complement of reports and dashboards provide total visibility into the status of each study, country, site and investigator to provide the information necessary to make the best decisions possible. - Comprehensive CTMS software - Integrated with Ennov Clinical Data Management - Clear visibility into investigational sites - Integrated workflow -
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Deep Lens VIPER
Deep Lens
VIPER automates the screening process from remote patient identification (at the point of diagnosis) to qualified enrollment. Utilizing artificial intelligence, VIPER identifies and matches patients to precision trials in the narrow window of opportunity through lab-agnostic genomic data ingestion, EMR and pathology data in a way that is customized to both the patient and to the research. VIPER searches the customized matching engine to find the best available clinical trials for a patients’ specific diagnosis—at the time of diagnosis. Through workflow integration, VIPER sends real-time notifications of a patient's eligibility for available clinical trials to the entire care team in the narrow enrollment window. VIPER also provides real-time interactive dashboards with rich data mining capabilities to aggregate site and study level patient data to hit your study KPIs. -
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AcceleTrial
LINEA System
AcceleTrial™ takes the guesswork out of clinical trial site identification and activation. Our Study Start-up Management System (SSMS) is based on the foundation of objective data and not self-identification. AcceleTrial™ gives you a database of thousands of sites globally that are ranked and indexed on the basis of: Objective Site-specific Therapeutic Expertise, Objective Site-specific Clinical Trial Experience and Objective Patient Data. Objectively pair the right sites globally with objective data on expertise, experience and patients to your clinical trials. Expediently launch the right sites to begin enrolling patients using AcceleTrial™ automated “push and pull” structure presented in multiple languages. Accurately collect required documents using pre-filled templates and track activities in real-time. Immediately start using system – cloud-based solution requiring minimal IT set-up or training. Simply integrate AcceleTrial™ with CTMS or other clinical trial systems. -
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Clinical Conductor CTMS
Advarra
Clinical Conductor CTMS is a cutting-edge clinical trial management system (CTMS) designed for hospitals, research sites, asset management companies, site networks, health systems, and contract research organizations (CROs). This cloud-based solution helps make the clinical trial process more efficient, thereby helping research organizations make better business decisions and meet every challenge. Key features include electronic data capture, study planning, enrollment management, document management, recruiting management, and more. -
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cubeCTMS
CRScube
cubeCTMS is a comprehensive clinical-trial management system designed to provide end-to-end oversight of trials, from site and investigator tracking, enrollment management and visit scheduling through budget and contract workflows, milestone reporting and document control. It centralizes study operations and automates key processes so sponsors, CROs and study teams can monitor progress in real time, manage tasks across multiple studies, improve site communications and mitigate risk. With built-in dashboards, alerts and audit-ready logging, cubeCTMS supports regulatory compliance (including FDA 21 CFR Part 11 readiness) and enables stakeholders to manage trial timelines, resources and performance from one platform. The system integrates with other CRScube modules (such as EDC, eTMF, pharmacy/RTSM) to provide a unified ecosystem that reduces duplication, improves data flow and supports adaptive workflows during amendments or global roll-outs. -
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Longboat
Advarra
Longboat is a cloud-based clinical trial support solution provides users with an integrated Guided Compliance toolset to guide them at all times. Longboat provides the clinical trial site staff with the right resources to let them focus on patients. Longboat allows patients to view essential study information and check visit reminders. Longboat allows users to seamlessly manage the controlled rollout of the amended clinical trial protocol. Centralize the secure exchange of regulated documents between sponsors, CROs, and sites, significantly streamlining study startup and eliminating historically cumbersome processes across research stakeholders. All key stakeholders—clinical operations, monitors, site staff, and participants—access one integrated support platform with content tailored to meet their specific needs. Provide your site staff the tools and resources they need to stay engaged and compliant while focusing on the participant. -
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Clinical Research IO
Clinical Research IO
The industry’s leading eSource, CTMS, and eRegulatory software for clinical trial sites. Capture source data seamlessly and in real-time with CRIO’s best-in-class electronic source. You’ll eliminate up to 90% of your paper and improve data quality by 80%. Take control of your operations with CRIO’s intuitive Clinical Trial Management System. Schedule patients, track financials, streamline recruiting, and more. Introducing electronic regulatory binders fit for the 21st century, which includes the first-ever electronic delegation log — all 21 CFR Part 11 compliant. For clinical trial sponsors: conduct 100% remote monitoring of your sites’ source data and regulatory documents in a secure, online portal. Join Our Network of 500+ Clinical Research Sites From Around The World. Our mission is to help you grow your business. We do that by streamlining your site’s operations, so that your studies don’t stop just because you aren’t in clinic. -
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Lindus Health
Lindus Health
Lindus Health is revolutionizing clinical trials with an all-in-one solution that delivers faster, more reliable results. Our comprehensive approach integrates full-service CRO capabilities, site operations, and advanced technology, streamlining every aspect of your study from design to data delivery. By leveraging agile in-house tech, we expedite site setup and patient recruitment, accessing over 30 million electronic health records to accelerate enrollment. Our fixed milestone, pay-on-results pricing model ensures aligned incentives, eliminating unexpected costs and delays. With an average satisfaction rating of 9.7/10, our responsive and experienced clinical operations team is dedicated to delivering excellence. Lindus Health has rapidly expanded its global presence, conducting over 91 trials across various therapeutic areas, including metabolic health, women's health, diagnostics, and medical devices. -
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ArcheMedX Ready
ArcheMedX
Pharma and biotech trust Ready by ArcheMedX to better equip their trial teams, improve decision making, and reduce study delays. Prevent the most common sources of study delays, by better understanding which sites and teams are most prepared to start and effectively conduct the study. Reduce time and costs spent resolving issues, especially early in the trial. Confidently know which sites truly understand your patient eligibility requirements. Enjoy knowing they’ll be better equipped to enroll eligible patients sooner, hit enrollment targets, and avoid screen failures. With detail down to each individual and study objective, you can know with confidence that trial team members truly understand the specifics of the protocol. Predict where risks lie so you can prevent them, and experience fewer deviations overall. -
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Cloudbyz eTMF
Cloudbyz
Cloudbyz eTMF solution offers a cloud-based repository of all clinical trial documents including files, images, information, etc. Digitally store, manage, and share all clinical trial-related documents with a centralized overview. Manage essential trial documents, stay inspection ready, and enable real-time visibility for CROs, sponsors, monitors, and other stakeholders in a clinical trial. Cloudbyz eTMF is built on the cloud, enabling Sponsors, CROs, and Sites to manage their trial documents with the highest levels of efficiency and integrity. The solution benefits are listed below - 1. Secure, reliable & scalable 2. Compliant & inspection ready 3. Flexible & easy to use 4. Real-time visibility of TMF completeness 5. Collaboration with Site/ Sponsor/CRO -
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Complion
Complion
Complion’s platform is the accepted standard built specifically for clinical researchers. Our solution ensures the highest level of compliance with the greatest efficiency and the least amount of work. Allowing you to focus on what really matters — advancing and improving patient outcomes. Whether you are a Research Site, Sponsor or CRO, our eReg solution can help you address any type of clinical trial challenge, now and in the future. Reduce costs, avoid redundancy, and increase staff productivity. Easily archive, get signatures and view files from anywhere or from any device. A built-in audit trail ensures accuracy and eliminates study conduct and patient safety risks. Our clients include leading cancer centers, medical centers, hospitals, and health systems, as well as multi-specialty practices and dedicated research sites. -
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Unlearn
Unlearn
Advancing AI to eliminate trial and error in medicine. Our digital twins enable confident and quick clinical trials. We work in neuroscience, immunology, metabolic disease, and more. TwinRCTs reach full enrollment sooner because they require fewer patients to achieve the same power as traditional trial designs. Shorten time to enrollment in late-stage studies. TwinRCTs improve the ability to observe treatment effects in early-stage studies by increasing power without adding more patients. Make confident decisions from early-stage studies and attract study participants. TwinRCTs give participants a greater chance of receiving the experimental treatment because they use smaller control groups. Position clinical trials with digital twins for regulatory success. Unlearn is engineering the future of medicine with artificial intelligence. We invent and deploy new types of generative models trained on extensive patient-level data from previous studies. -
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SiteCentric
SiteCentric
SiteCentric is a unified clinical trial management platform built by research sites for research sites, consolidating CRM, eISF, CTMS, finance, and reporting into a single system. It standardizes and automates workflows across the entire trial lifecycle, nurturing study leads and organizing pipeline activity with a purpose-built CRM; centralizing budgets, contracts, eReg, training records and source documentation for rapid startup; boosting enrollment through targeted outreach and querying existing databases; tracking patient visits and capturing high-quality eSource data; running internal QC checks, version control and audit-ready eISF documentation; managing budgets, invoicing, payment reconciliation and patient reimbursements; and delivering leadership dashboards to uncover performance metrics and trends. -
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Curebase
Curebase
Select Curebase to run your next study and experience greater diversity, faster enrollment, and better retention. Our cutting edge approach allows patients to participate at home and with community physicians leading to faster, cost effective, and diverse studies. Curebase has a unique combination of in-house virtual CRCs paired with a global network of virtual PIs working together with community doctors to bring studies to patients anywhere. Most patients don't live near a traditional research site. Our trials move the research into patients' homes and real-world medical settings, such as community doctors' offices. Curebase infectious disease trials successfully enroll patients utilizing a new kind of model that meets patients where they are through community healthcare and virtual settings. -
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Medidata
Dassault Systèmes
The Medidata Clinical Cloud is our cutting-edge platform that transforms the clinical trial experience for patients, sponsors, CROs, and research sites. As the only unified technology platform dedicated to clinical research, the Medidata clinical cloud addresses the holistic research process from start to finish. Our platform helps life science and medical device organizations cut development costs, mitigate risks, and deliver treatments and devices to market faster. No matter which products you choose for your clinical trial program, you will have access to the power of the Medidata Clinical Cloud. At Medidata, we’re leading the digital transformation of clinical research. Powered by artificial intelligence, machine learning and advanced analytics, our platform brings researchers, study managers, investigators, and patients together to accelerate research. Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials. -
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Zapclinica
Zapclinica
Manage your clinical trial in one platform. Zapclinica is an eClinical suite designed to manage and conduct every aspect of your decentralized clinical trial - hybrid or virtual. Automate complex processes, identify outliers, optimize resources, improve decision making and collaboration between sponsors, CROs, and sites. Zapclinica reduces the time and costs to run a successful clinical trial. Manage your clinical trial in one platform. Zapclinica is an eClinical suite designed to manage and conduct every aspect of your decentralized clinical trial - hybrid or virtual. Automate complex processes, identify outliers, optimize resources, improve decision making and collaboration between sponsors, CROs, and sites. Zapclinica reduces the time and costs to run a successful clinical trial. Cover all aspects of your study with one platform. No extra vendors, no extra third-party, choose the app you need in a single environment, including EDC, ETMF, Payments, Logistics, and many more. -
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Ripple Science
Ripple Science
Ripple is a web-based software solution and active registry that facilitates the recruitment and management of research participants for clinical, translational and social science studies. Built from the ground up by researchers for researchers to truly transform participant workflow, Ripple is an end-to-end research participant management software that accelerates the entire research life cycle. Applying technology to solve patient recruitment and retention challenges, the #1 reason cited when clinical trials fail. The success of clinical trials and translational studies greatly depends on the ability of research teams to meet enrollment targets on time and on budget. Ripple Recruit empowers research teams with the automation tools and analytics necessary to accelerate the recruitment processes and maximize the likelihood of study success. Ripple Recruit provides critical insights into your recruitment campaign and workflows, including what sources are most effective. -
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Trialbee
Trialbee
Trialbee’s Honey Platform centralizes global patient recruitment by funneling all referrals into a single, vendor-agnostic dashboard, standardizing data across every recruitment partner, and providing actionable site and candidate insights with visual ROI metrics for each partner. Its Precision Recruitment module builds data-driven patient profiles, delivers live medical secondary screening, and executes hyper-targeted digital outreach to qualify ideal candidates. Complementing this, Omnichannel Solutions leverage a curated ecosystem of community advocates, pharmacies, labs, and other proven partners, fully integrated and transparently managed within Honey, to expand reach into diverse patient populations. Real-time analytics and robust ROI reporting empower trial operations teams with hands-on success guidance and actionable insights, streamlining complex compliance requirements and optimizing enrollment strategies in one intuitive SaaS platform. -
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DrugDev Spark
IQVIA
DrugDev Spark™ is the world’s first comprehensive unified clinical operations suite. Explore our solutions below to learn why so many sponsors (including 9 of the top 10) and CROs (including 4 of the top 5) trust DrugDev technology. DrugDev Spark™ is the industry’s first comprehensive unified solutions platform – comprised of innovative technology and expert services proven to add value on thousands of clinical trials. From planning through closeout, our solutions are rigorously tested and improved by sponsors, CROs and sites of all sizes, in more than 60 countries. Through this experience, we have established and integrated best practices into every feature of our system. That’s why 9 of the top 10 pharma, 4 of the top 5 CROs, and the biggest industry collaborations are among the many organizations that trust DrugDev technology. Most of the world’s top sponsors and CROs are using DrugDev solutions to transform how they run clinical trials through collaboration. -
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ePharmaSolutions
ePharmaSolutions
At ePharmaSolutions, we are building something new. We are not a high-tech company. We are an idea company whose thinking is highly entrenched in technology, but not limited by it. We support the drug development industry with solutions that improve the identification, activation, training and management of clinical trial sites. With new perspectives on old problems, we deliver technology-enabled solutions that help to “un-complicate” the chaos of clinical trial management. ePharmaSolutions (ePS) is a leading provider of e-clinical solutions that improve the way that clinical trial sites are selected, trained, activated, and managed. By applying fresh thinking to old problems, we deliver clever, technology-enabled solutions that empower sponsors, contract research organizations and investigator sites to “un-complicate” the chaos of clinical trial management. -
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Studypages
Studypages
Studypages is a comprehensive clinical trial management software designed to unify participant experiences and streamline clinical operations. It offers a suite of tools that facilitate participant engagement, site management, sponsor oversight, communication, collaboration, and workflow automation. By integrating these functionalities into a single platform, Studypages enhances the efficiency and effectiveness of clinical research, accelerating the development of medical innovations. -
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AutoCruitment
AutoCruitment
AutoCruitment provides a direct-to-patient, web-based technology platform that seamlessly recruits, qualifies, and automatically refers the right patients for your clinical trials. It combines global direct-to-patient recruitment technology and methodology to target, recruit, screen, and refer patients by eliminating dependencies on provider approval, medical record access, and investigator sites. It leverages online browser behavior and geotargeting across 1,500 digital channels, including search, display, social media, and partner mobile, to reach and pre-qualify patients in real time using sophisticated online screeners based on inclusion/exclusion criteria. Research sites access a secure, user-friendly portal that delivers instant referrals, customizable reports, and live-tracking dashboards, while dedicated project management and site engagement teams work holistically to optimize randomization rates. -
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Deep 6 AI
Deep 6 AI
Deep 6 AI disrupts the clinical trial enrollment process by transforming the way researchers identify eligible patients. Using artificial intelligence and natural language processing to mine structured and unstructured patient data, DEEP 6 AI finds more, better-matching patients for trials in minutes, not months. Deep 6 AI works with some of the most prominent health systems, pharma companies, and CROs in the world --making the DEEP 6 platform a crucial step in their clinical research workflow and greatly accelerating patients’ access to clinical trials. Deep 6 AI finds more patients for clinical trials in minutes rather than months, getting life-saving cures to people more quickly. Deep 6 AI’s software analyzes structured data, such as ICD-10 codes, and unstructured clinical data, including doctor’s notes, pathology reports, operating notes and other important medical data in free-text form that cannot be searched easily. -
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Inato
Inato
We’re building a global clinical trial marketplace to create greater visibility, access, and engagement across a more diverse population of doctors and their patients. At Inato, we’re on a mission to bring clinical research to each and every patient, regardless of who they are and where they live. Marketplaces have proven transformational in broadening access to many, we believe that we can achieve this in clinical research. We shine a light on the hundreds of community sites around the world that are looking to offer more trials to their patients, while helping them realize their full research potential. We reliably match the right sites to the right trial on a global scale. Our end-to-end support model ensures sponsors can confidently partner with a broader range of sites around the world. Matching research sites to the right clinical trial protocols, unlocking site potential worldwide. -
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SimpleTrials
SimpleTrials
SimpleTrials is an on-demand, subscription-based Clinical Trial Management System (CTMS) designed for sponsors, Contract Research Organizations (CROs), and investigative sites. It offers a comprehensive suite of tools to effectively plan, manage, and track clinical study portfolios, including features such as site startup and subject tracking, document management with integrated electronic Trial Master File (eTMF), real-time study analytics, calendar and monitoring, custom fields and trackers, ad-hoc reporting, planning and milestones, site contracts and payments, and electronic visit reports. It supports compliance with 21 CFR Part 11 and provides a secure, validated environment for clinical trial data. Users can customize tracking views, integrate with various Electronic Data Capture (EDC) systems, and utilize built-in templates for consistent document management.Starting Price: $849 per month -
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REDCap Cloud
REDCap Cloud
REDCap Cloud is a unified data-science platform that enables organizations to collect, integrate, standardize, analyze, and share real-world and regulatory-grade clinical and research data using a single standards-based system. It supports the full lifecycle of randomized clinical trials and real-world evidence studies by offering modules for complex trial design and deployment, a clinical data hub that converges eCRF and non-eCRF sources, real-time operational and data insights via AI/ML, eSource and EHR connectivity, patient engagement (ePRO/eCOA, wearable devices) for hybrid or decentralized trials, analytics including synthetic control arms and digital twins, and global compliance with security standards, all built to reduce data-silos, eliminate vendor fragmentation, deliver bidirectional data flows and give sponsors, CROs and health-systems end-to-end visibility and control across site performance, study data quality and regulatory readiness. -
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Judi
Judi
Judi is a cloud-based clinical-trial collaboration platform built to simplify, secure, and streamline complex workflows across sponsors, CROs, trial sites, and partners. It supports a full range of trial functions, from endpoint/event adjudication, central eligibility review, data-safety-monitoring, remote monitoring, medical imaging, and site/user qualification, to fully custom workflows (Judi Flex). Judi replaces manual processes, spreadsheets, untracked emails, or siloed file-sharing tools with a unified, compliant workspace: every document, communication, image, query, and decision goes through secure, traceable pipelines. Built-in features include role-based permissions, audit trails, real-time chat, query management, dashboards and worklists, flexible document submission and review, eCRFs with edit checks, and reporting tools, making trial data collection, review, and reporting far more efficient and less error-prone. -
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ClinOne
ClinOne
ClinOne connects, informs, and empowers participants, care partners, and sites in clinical trials with a true single platform for trial awareness, consent management, and participant experience/retention, underpinned with comprehensive data insights tools and standards-based interoperability. The platform offers solutions such as Site Hub, a one-stop shop for sites to access necessary resources, including inclusion/exclusion criteria, site resources, systems landing page with single sign-on, and community features. The Connect module includes Sponsor & Monitor Hub, trial awareness, healthcare provider community, site selection, and diversity, equity, and inclusion data. The Inform module provides consent management, education, eConsent with eSignature, data insights and modeling, tele-visit capabilities, and community collaboration. The Empower module offers transportation management, medication adherence monitoring, care partner and caregiver portal, and more. -
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Clinical Concepts
IVR Clinical Concepts
IVR Clinical Concepts specializes in providing virtual clinical trial technology and patient engagement solutions. Their offerings include electronic patient-reported outcomes and patient diaries, which aim to deliver better data with fewer errors, resulting in shorter timelines and lower costs. They also provide patient recruitment and outreach services, focusing on outreach, pre-screening, and real-time data collection. Their subject screening, registration, and randomization solutions are described as modular, custom, flexible, and configurable. Additionally, IVRCC offers clinical trial material management solutions designed to reduce workload while providing more control, as well as eClinical integration services to seamlessly thread data together. Their chart review services provide real-world data and clinical insights. IVRCC emphasizes custom, modular, and configurable solutions to improve the patient experience and optimize clinical trial success. -
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ImproWise
Core Clinical Services
ImproWise – a 100% web-based, secure, and HIPAA compliant platform designed for end to end Clinical Trial Management (CTMS) and Clinical Data Management (CDMS). ImproWise offers unparalleled flexibility, speed, and security, combining CTMS, CDMS, EDC, CTBM, CTPM, eTMF, ePRO, and RBACS functionalities. ImproWise is crafted to meet the needs of every stakeholder in clinical trials. From sponsors and investigators to data managers, data entry specialists, site staff, and regulatory affairs professionals, our platform ensures seamless collaboration and efficiency. -
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Datacubed Health
Datacubed Health
Discover the industry’s most innovative approach to clinical outcomes and patient-reported outcomes data. For instance, our robust solution extends beyond simple data entry capabilities and enables a truly patient-centric study. While our eCOA software is rooted in behavioral science, it is also purpose-built by clinicians to meet the expectations of sites and sponsors. Personal identity, coupled with motivational intervals, and meaningful goals. Unlike other eCOA solutions, the Datacubed app has an easy-to-use interface allowing participants to get right to what’s essential. As has been noted, collecting data has never been easier, thanks to our intuitive, flexible, and interactive app. Flexibility in trial design has become paramount; for this reason, we offer data capture in person, remotely, or in combination to meet the needs of traditional, hybrid, and virtual trials. -
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WCG ClinSphere
WCG
WCG ClinSphere is a trailblazing approach for running clinical trials end to end. Leveraging the power of artificial intelligence, the platform connects sites, sponsors, CROs, and participants in one unified cloud platform. One place to manage your trial efficiently from start to finish. The WCG ClinSphere platform architecture is underpinned by four tenets of efficiency. Our unsurpassed clinical dataset feeds into a federated AI learning model, enabling smart automation across the clinical trial lifecycle. Access up-to-the-minute reports and insights to stay informed and make timely decisions. Simplify tasks and enhance accuracy with easy-to-understand workflows that guide you every step of the way. Streamlined logistics, operations, and processes throughout the clinical research journey. The power of vast data stores and deep analytics to make the connections necessary for faster clinical research. -
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GRAVITY
ASSAY Clinical Research
In clinical research, being organized is a prerequisite of success. Bringing the right resources to bear at the right time is a challenge. This is particularly applicable for document management for a clinical trial. GRAVITY is your long-time solution for site file and trial master file management. We have converted both files into easy to manage, co-ordinated electronic format. This integrated package facilitates logical and convenient document management. Being an integrated eTMF and eISF system, GRAVITY becomes a complete cloud-based electronic DMS, Serving as a window for sponsors, CROs, and Sites. However, GRAVITY can also be deployed and utilized for each individual entity alone. when a site is selected for conducting clinical trial, Documents start to flow in, however, the initial pack of essential documents require maintenance. GRAVITY incorporates a unique features of overseeing the essential document management and alerting the users of expiring documentation. -
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Signant Health
Signant Health
Signant Health is a global evidence-generation company that helps modernize clinical trials by meeting patients where they are and reimagining the path to proof. They offer comprehensive clinical technology solutions, including electronic Clinical Outcome Assessments (eCOA), Electronic Data Capture (EDC), electronic clinician ratings, and a unified eClinical platform. Their patient engagement tools encompass a patient engagement app, eConsent, and telemedicine capabilities. Signant Health also provides clinical data and analytics services, such as COA data analytics and data aggregation and intelligence. With over 30 years of experience, they have supported thousands of trials and contributed to hundreds of drug approvals, making them a trusted partner for sponsors and CROs aiming to deliver high-quality data for trial decisions and regulatory submissions. -
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TCS ADD
Tata Consultancy Services
TCS ADD platform accelerates speed-to-market for pharmaceutical industry across the entire clinical R&D value chain and helps make clinical trials more agile and safe. TCS ADD enables digital ecosystems, simplifies data complexity and provides faster access to new and effective drugs for the patients. The platform is powered by cognitive artificial intelligence engine called TCS Decision FabricTM, smart analytics and IoT that provides superior business value to pharmaceutical industry. A next-generation and end-to-end metadata-driven solution to manage industry & sponsor clinical standards. A data science-driven platform that leverages AI & ML technologies to enable quicker decisions, faster study start-up and targeted interventions. A solution that digitizes the entire clinical trial supply management process while putting the patient in the center, increasing patient’s safety and overall efficacy. -
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Science 37
Science 37
Science 37 is a clinical research company specializing in decentralized clinical trials through its Metasite model, which eliminates physical proximity as a barrier, enabling patients to participate from anywhere. This approach expands access to over 90% of patients who are unable to participate in traditional site-based research, offering the recruiting power of 20 sites in one and providing the flexibility patients need to participate from anywhere. The Metasite is powered by a proprietary platform that drives uniform study orchestration, guiding the workflow of patients and study staff, and capturing study data without the need for manual reentry. This centralization of people, processes, and platforms delivers built-in protocol compliance, ensuring greater compliance and high-quality data. Science 37's in-house medical teams, telemedicine investigators, and mobile nurses have extensive experience in remote trial conduct across various therapeutic areas, ensuring broad reach. -
45
YPrime
YPrime
eCOA and digital technologies are the future of clinical research, effectively bridging the gap between traditional and forward-looking, patient-focused development. Rely on YPrime’s eCOA solutions not only for high quality patient data, but for a different and better user experience -- across sponsors, investigator sites and patient users. YPrime employs an agile software development approach to quickly customize and configure functions tailored to the needs of the study in 8-12 weeks. Our interactive and visual build process ensures clients have opportunities to see the system at different stages during design and development, prior to go-live. Our pre-validated, configurable authoring environment facilitates start-up timelines and post-production changes, such as protocol amendments. -
46
Altis Labs Nota
Altis Labs
Altis Labs announces launch of Nota – a clinical information platform to accelerate therapeutic R&D Nota leverages. AI to predict patient outcomes from imaging data so sponsors can better prioritize their most promising therapies. Nota enables researchers to operationalize clinical trial imaging data, access predictive imaging biomarkers, and accelerate R&D at scale. Using Altis’ cloud-based software platform powered by deep learning, biopharma can incorporate comprehensive outcome predictions at the image, patient, and cohort level to improve clinical trial design and more confidently anticipate clinical endpoints. Such insights have the potential to significantly accelerate development timelines, lower drug development costs, and improve the likelihood of trial success across therapeutic areas. -
47
Sano
Sano
Sano Genetics provides an end-to-end, 360° platform for precision-medicine and clinical-trial research that unifies patient recruitment, genetic testing, consenting, and long-term engagement to dramatically speed up and simplify study workflows. It supports custom protocol development and ethics submission documentation, digital prescreening and consent, and recruitment support through online campaigns, partner networks, and patient-advocacy groups, enabling sponsors and CROs to reach niche patient cohorts or underrepresented populations across multiple geographies. Sano offers at-home, non-invasive saliva-based DNA testing kits (as a cost-effective alternative to clinic blood draws), logistic support for sample collection and processing, reliable genetic and biomarker testing via certified labs, bioinformatics, and return of results, including genetic counselling when needed. -
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CTMS Master
Anju Software
Premier clinical trial management system designed specifically to help overcome technical challenges associated with managing clinical trials. CTMS Master improves user accessibility and communication, reduces manual operations, and eliminates redundant data and tasks, allowing a more efficient trial conduct. An integrated Site Visit Report tool with automated workflow eliminates duplicate data entry and facilitates the creation of out-of-the-box Site Visit Reports (SVR). Maintain standard templates for project and site documents, events, milestones, site visit reports and budgets that are tailored as needed for each study. CTMS Master provides 100+ metrics/statistics for clinical study projects, countries and sites as well as 80+ standard reports plus ad hoc reporting capabilities. With CTMS Master, you can define site-specific budgets from a default budget template, track accrued payments and future obligations, define automatic or manual approval of each payment type, and more. -
49
TrialKit
Crucial Data Solutions
TrialKit is a unified eClinical platform that brings mobility, automation, and efficiency to modern research teams. Accessible from any browser or native app (iOS, Android, and Mac), TrialKit supports rapid study setup, real-time data collection, and centralized oversight—ideal for CROs and sponsors seeking agility without compromising compliance. Its drag-and-drop design tool makes it easy to build studies quickly, while advanced features like AI-powered reporting and mobile ePRO/eCOA enhance visibility and decision-making. Trusted by over 40,000 across the globe, TrialKit enables teams to work smarter from first patient in to database lock. Recognized with the 2024 SCDM Innovation Award, it’s the all-inclusive solution for today’s studies. -
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Clinials
Clinials
Clinials Trial Search simplifies complex trial info using AI, boosting participant engagement and enrollment rates. Benefits: Enhanced Engagement: Empowering potential participants with plain language descriptions. Wider Reach: Access a diverse pool of eager participants seeking clinical trial opportunities. Listing on Clinials Trial Search is free. We also offer referral fees from $300- $5,000 based on trial complexity.Starting Price: $300
