Alternatives to Longboat
Compare Longboat alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to Longboat in 2026. Compare features, ratings, user reviews, pricing, and more from Longboat 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. -
2
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. -
3
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. -
4
Teckro
Teckro
Teckro clinical trial software connects all study stakeholders to critical information. Every time. Everywhere. We find answers every day from our smartphones. Why shouldn’t the same be true for clinical trials? Critical, up-to-date study information always at hand when and where research staff and CRAs need it. Study answers are just a tap away on any mobile device, giving research staff a direct line to crucial details. And when updates or amendments are needed, site staff and monitors can be alerted in real-time. Cloud-based clinical trial software, Teckro is up and running quickly with nothing to install. It’s simple, easy and intuitive. Teckro is securely hosted and compliant with major industry regulations, including FDA 21 CFR Part 11. Only the right, approved version of study documents, means no more worrying about version management. -
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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. -
6
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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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. -
8
Oracle Clinical One
Oracle
Clinical One RTSM can support a randomization strategy for the simplest to the most complex studies without the need for programming or coding, which eliminates the need for prolonged user acceptance testing. Take control of your study through self-service configurations and build a study in days instead of weeks. Assess the status of the drug inventory and make modifications in real-time without reverting to the vendor and incurring cost and change requests. Eliminate change request costs and avoid delays by quickly implementing changes and promoting your studies in seconds. The only platform that truly unifies people, processes, and data to simplify and accelerate the clinical trials of the future. Virtual components in clinical trials allow greater patient participation and significantly improve clinical trial data quality. Transformative digital strategies are needed for faster study startup to harmonize data from any source and to streamline workflow. -
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Mosio
Mosio, Inc.
Mosio enables research teams to improve subject adherence, communications, and data collection on mobile’s most popular channel: text messaging. Our software makes research teams more efficient in how they communicate with study participants through messaging automation and interactive elements delivered to participant mobile phones. WHO WE HELP: + Clinical Trial Sponsors (Pharma and Biotech) + Cancer Centers and Clinical Research Organizations + NIH-Funded Studies + Public Health Agencies + Clinical Trial Managers, Clinical Operations Managers/Directors, Clinical Project Managers, Principal Investigators, Clinical Research (Study) Coordinators, and any research staff who communicate regularly with study participants. BENEFITS: + Interactive dosing reminders and medication adherence alerts. + Automate data collection. + Increase engagement and adherence. + Fix your no-show problem with SMS appointment reminders. + Improve retention with automated check-ins.Starting Price: $99/month -
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Biorce Aika
Biorce
Biorce’s Aika is an AI-native clinical intelligence platform that accelerates every stage of the clinical trial lifecycle by replacing slow, manual protocol development and feasibility assessment with explainable, evidence-based automation. Built on insights from around one million real global trials, it generates first-draft study protocols, complete regulatory documentation, site feasibility assessments, risk and data management plans, and other essential trial artifacts in a fraction of the time traditional methods require, helping reduce delays and costly amendments. Aika provides full transparency into how it reaches recommendations so teams can confidently present choices to regulators and maintain expert control, blending AI speed with clinical expertise. It minimizes trial preparation timelines from weeks to days, cuts the number of amendments, and lowers overall risk while integrating seamlessly into existing workflows without heavy retraining. -
11
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 -
12
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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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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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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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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MAISi
Agile Health Computing
Until now, the options available for managing clinical trials at an investigator site were either keeping multiple shared spreadsheets or buying expensive software unsuited to Australian conditions. MAISi is the game-changer. Beginning as a repository for clinical trials data at a major hospital in 2001, MAISi has evolved into a sophisticated workflow application to assist in most aspects of a research unit’s operations. MAISi acts as a central repository of data to store information about studies and the business units that run them. The datasets are arranged to support management decision-making. Staff in each business unit have access to the data (Studies, Patients, Investigators, Study Team Members) associated with their own business unit, whereas staff granted global access (normally Financial Officers and System Administrators) have access to all data. -
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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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Folio3 Clinical Trial Management
Folio3 Digital Health
Folio3 Digital Health's Clinical Trial Management Software (CTMS) is a comprehensive, web-based platform designed to streamline the entire clinical trial lifecycle for pharmaceutical companies, CROs, and research organizations. It centralizes trial operations, from planning and site management to data collection and reporting, ensuring compliance with global regulations like FDA 21 CFR Part 11, GxP, and HIPAA. The software emphasizes user-friendly interfaces, real-time dashboards, and scalable modules to handle trials of any size efficiently. Core Modules The platform features dedicated modules for study setup, where users define protocols, timelines, and budgets with customizable templates. Site management tools track investigator qualifications, contracts, and payments, while patient recruitment capabilities include screening, enrollment tracking, and visit scheduling with automated reminders.Starting Price: $300 -
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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. -
20
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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Arone
Arone
With over 20 years of experience in both software edition and clinical research sectors, Arone provides clinical research organizations with a complete suite of tools for patient data entry and management. Our solutions are turnkey and our team provides you with personalized support for the proper conduct of your projects and studies. Collect and manage patient data in a single tool. Arone manages the randomization of patients by randomly assigning study participants a type of treatment in order to remove bias in the study. Empower participants of clinical trials for their daily data entry. Benefit from a customized support for your projects. -
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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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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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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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Elligo Health Research
Elligo Health Research
Clinical trials and research traditionally existed outside of the care administered within local hospitals and physicians’ offices. Physicians weren’t always aware of what research was being conducted, and patients had little idea research that could potentially improve their outcome or benefit their health was occurring at all. Only Elligo enables broader participation in clinical research than ever before with access to over 150 million patients and their data, allowing physicians to provide research as a care option to patients who otherwise wouldn’t have access to clinical research. Traditional recruitment methods are constrained by limitations such as patient proximity to a specific site where research is conducted. Research has also shown that patients prefer to engage in a study with their trusted healthcare physician. -
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ez-SourceDocx
Alpha Clinical Systems
Maximize data quality. Ensure data quality by capturing eSource data directly during the patient visit. With built-in edit and validation checks, users capture high-quality data electronically, dramatically reducing errors and queries—and delivering data for real-time, remote monitoring. Reduce study time, cost and risk. Promoted and endorsed by the FDA to streamline and modernize clinical trials, purpose-built eSource eliminates slow, error-prone and inefficient SDV and transcription into EDC systems. Streamline site, study efficiency. Designed with site users in mind, ez-SourceDocx streamlines workflows, reduces workload and ensures protocol execution by guiding sites through properly sequenced visit procedures that guarantee all end point data and prompt quality investigator evaluation. -
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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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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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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. -
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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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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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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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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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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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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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Cenduit IRT
Cenduit
Today’s Interactive Response Technology (IRT) systems are increasingly complex. Flexible and configurable IRT matters - with IRT data as the source of record for recruitment, clinical trial drop-out rates, patient visits, and other crucial data. Choose a platform that’s user-friendly, mobile-ready, and comprehensive - embedded in quality, flexibility and expertise. Choose comfort with complex therapeutic expertise in today’s risk-based eClinical environment. Combining the right technology, subject matter expertise and commitment to service we empower clinical trials to deliver patient outcomes. Deep clinical and supply chain knowledge drives innovation and provides clients with control over their Randomization and Trial Supply Management (RTSM) processes. Our innovative suite of tools drives distinctive levels of quality control, site efficiency and patient compliance. Our IRT platform can meet the needs of almost any study, enabling fully validated deployment in as little as 30 days. -
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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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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. -
39
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. -
40
OneStudyTeam
Reify Health
We build solutions that connect and empower the clinical trial ecosystem. The Enrollment Performance Management platform that sites love and sponsors depend on. Used by 2,000 research sites across 26 countries and by half of the top-20 global biopharma companies. Sites spend less time with redundant and manual tasks so that they can move patients forward. Less double work for sites. Fewer logs, phone calls, and emails for both sites and sponsors. Sponsors can optimize enrollment proactively with real-time access to novel pre-screening and enrollment data. Surprisingly simple patient recruitment and enrollment solution trusted by more than 1,800 sites across 26 countries. Access powerful recruitment and enrollment insights to run faster, more predictable clinical trials. Eliminate redundant work so you can get back to the work that matters most: helping patients. Manage recruitment across all trials, sponsors, or CROs. Enter information once and it goes where you need it to go. -
41
Replior
Replior
An integrated EDC, eConsent, ePRO and Virtual Visit platform for the efficient conduct of clinical trials. Replior is a company providing software for clinical trials. Our suite of systems is called Trial Online and enables collection and management of data from investigators, participants and wearables in an easy and efficient way. Trial Online supports decentralized clinical trials (DCT) by enabling the trials to operate with site visits, remote visits or as a hybrid. We started our journey 20 years ago with a request to build an online CRF service for one of the world’s largest pharma companies, back then we were an IT operations provider for the pharma industry. This was the starting point of providing software for collection of data in clinical trials. Today we offer a full suite of data collection software services, and our IT operation is performed by our, very certified, sister company Complior. -
42
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 -
43
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. -
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Clinion eCOA
Clinion
Clinion eCOA enables you to run decentralised clinical trials with patients participating remotely, using eConsent and patient diary for higher compliance Clinion eCOA allows study participants to report their health using their own smartphones, from the comfort of their homes; allowing clinicians to monitor patients in real-time. Clinion eCOA is fully integrated with Clinion EDC and allows trial participants to input daily outcomes directly, eliminating data duplication and transcription errors and providing clinicians with a real-time view of patient progress. The eCOA app supports multilingual forms that simplify patient engagement and generate cleaner data. The decentralised nature of eCOA allows wider and faster patient recruitment. -
45
Clin'form
Kayentis
Clin'form is a flexible, robust, and comprehensive electronic Clinical Outcome Assessment (eCOA) platform designed to streamline clinical trials for patients and sites, enhance data quality, and accelerate processes for research teams. It is adaptable to all protocols and populations, effective for any type of questionnaire (PRO, ObsRO, ClinRO, Diary), and caters to all age groups, from pediatric to older patients. The platform accommodates any population size, capable of managing studies ranging from a handful to over 10,000 patients across all geographic regions. Clin'form offers seamless integration with other clinical systems, ensuring a smooth workflow, and supports flexible data collection modes, including provisioned tablets or smartphones, the patient's own smartphone, web access from any browser, and interviews. Key features include an embedded tele-visit feature to plan for the unplanned, patient engagement modules to ensure high patient compliance. -
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Clinical StudyPal
Delve Health
Everything we do for your team starts with our blended, multi-modal platform. Comprehensive and fully configurable, Clinical StudyPal is a patient-centric technology designed to make your research faster, easier and more cost effective. As an app, it builds collaboration and engagement among sites and patients. As a web interface, it effectively manages your studies through powerful analytics. And as a notification solution, it keeps your patients and study team always in the know. What can Clinical StudyPal do for you? The real question is, what can’t it do? From our proprietary technology to our patient-centric offerings, our team is dedicated to providing yours with whatever it takes to achieve a smooth, successful trial experience. -
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Zelta
Merative
Zelta is a cloud-based unified clinical data management and acquisition platform with adaptable modules that can be tailored to meet the unique needs of your clinical trials program and accelerate outcomes. It offers features such as electronic data capture, clinical operations tools like randomization and trial supply management, clinical trial management system, electronic trial master file, and patient and provider engagement solutions including electronic clinical outcome assessments and electronic consent. Zelta is designed to manage clinical studies across all phases, therapeutic areas, and regions, providing a user-friendly interface and seamless access through single sign-on from anywhere in the world. The platform emphasizes flexibility and scalability, allowing for customization to align with specific study goals and the integration of solutions from both Zelta and other technology vendors. -
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Suvoda
Suvoda
Suvoda is a global clinical trial technology company specializing in complex, life-sustaining studies in therapeutic areas such as oncology, central nervous system disorders, and rare diseases. Founded in 2013, Suvoda offers an integrated platform that includes Interactive Response Technology (IRT), electronic Consent (eConsent), electronic Clinical Outcome Assessments (eCOA), and ePatient solutions, all designed to manage critical patient interactions efficiently. Their patented software architecture ensures a seamless user experience, facilitating precise randomization, drug supply management, and real-time data collection. Committed to enhancing patient comprehension and reducing site burdens, Suvoda's solutions are built to adapt to the evolving complexities of clinical trials. Headquartered near Philadelphia, with offices in Europe and Asia, Suvoda has supported over 1,500 trials across more than 85 countries. -
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assisTek
assisTek
AssisTek is a leader in innovative clinical technology solutions for clinical research, offering custom clinical software solutions to streamline and enhance patient data collection. With over 25 years of excellence, they have supported more than 800 clinical research trials across 46 therapeutic areas, including over 500 multinational Phase I–IV clinical trials. Their eCOA solutions are highly scalable, customizable, and efficient, powered by a proven, cloud-based technology platform. AssisTek's product suite includes TEK eCOA Tablet, designed to support any questionnaire used in a clinical trial, TEK eDiary for capturing patient-reported outcomes at home, TEK Configurator for building clinical trial projects from start to finish, and TEK Study Portal for eClinical tracking, training, and reports in one place. Their systems and services have made them the top choice for collection and analytics among patients and clinicians. -
50
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.
