Alternatives to TCS ADD
Compare TCS ADD alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to TCS ADD in 2026. Compare features, ratings, user reviews, pricing, and more from TCS ADD competitors and alternatives in order to make an informed decision for your business.
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Castor EDC
Castor
Castor is a leading platform for clinical data management, offering advanced solutions for electronic data capture (EDC), patient-reported outcomes (ePRO), and eConsent. Designed to streamline clinical trials, Castor enables researchers to efficiently collect and manage data from multiple sources in a compliant, user-friendly environment. The platform also supports decentralized trials (DCTs), providing tools for remote patient recruitment, monitoring, and real-time data analysis. Castor is trusted by over 50,000 users globally, helping clinical research teams accelerate trials while ensuring high-quality data and regulatory compliance.Starting Price: $100.00/year -
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ClinCapture
ClinCapture
At ClinCapture our mission is to build software that saves lives. Our technology lowers the cost of clinical trials by streamlining data capture processes while providing a platform that protects patient privacy. Clincapture advances the evaluation and development of drugs, biologics, and devices that demonstrate promise for the diagnosis and/or treatment of a wide range of diseases or medical conditions. -
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IQVIA
IQVIA
Thousands of organizations around the world trust IQVIA to speed drug development, ensure product quality and safety, improve commercial effectiveness, get the right treatments to patients, improve access to and delivery of healthcare, and ultimately drive better health outcomes. Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster. With a foundation in data, advanced analytics, and expert insight, IQVIA brings specialized capabilities to customers across the healthcare ecosystem. Read and watch the latest from IQVIA data scientists, doctors, researchers, and other subject matter experts on the topics that matter to you. From industry trends to how we are applying our capabilities to help, you can find it here. -
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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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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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Koneksa
Koneksa
Koneksa is a leading digital biomarker company for the pharmaceutical and biotechnology industries, specializing in developing, testing, and validating digital biomarkers to help clients understand the impact of their treatments on patients. Founded in 2013, Koneksa provides end-to-end remote clinical trial support, leveraging digital health technology, therapeutic expertise, and rapid patient-friendly remote data collection to gain better insights into patient health. Their validated, novel data algorithms are ready to deploy in treatment development programs, enabling the identification of signals earlier and faster than traditional measures. Koneksa's cloud-based SaaS platform allows multiple endpoints to be fed in real-time, giving immediate access to data and empowering confident, cost-saving decisions early in trials. The platform's ability to collect high-volume remote data with increased frequency offers ecologically valid measures and opportunities to reduce sample size. -
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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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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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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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Over the last several years, the Life Sciences industry has faced nearly $15 billion in fines and compliance-related settlements, making it critical for companies to adhere to pharmaceutical, medical device and biotech best practices. Efficient and effective management of clinical trials can also significantly impact the time, scope and budget for the development of a drug or medical device. With OpenText™ Clinical Trial Quality Management System (ctQMS), companies can remain compliant, reduce costs of records management and establish best practice through collaboration before, during and after the clinical trial lifecycle.
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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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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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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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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. -
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Cytel
Cytel
Cytel is a leading global provider of clinical trial design software, biometric services, and advanced analytics, specializing in optimizing clinical trials and assisting pharmaceutical companies in unlocking the full potential of their clinical and real-world data. Founded in 1987 by distinguished statisticians Cyrus Mehta and Nitin Patel, Cytel has been at the forefront of adaptive clinical trial technology and biostatistical science. Our software solutions, including the East Horizon platform, empower precise trial design and simulation, utilizing adaptive and Bayesian tools to optimize protocols and accelerate drug development. The East Horizon platform integrates key components of Cytel's trusted software portfolio into a unified solution with R integration, enhancing trial design capabilities. Additionally, Cytel offers the Xact software suite, a comprehensive toolkit for statistical analyses of small datasets, and sparse, and missing data. -
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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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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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FICS
Pi Health
Accelerating the development of lifesaving medicines and enabling patients globally to have equal access to the highest quality of cancer care and research. Our software is revolutionizing patient access to innovative medicines & clinical trials. FICS is an innovative software that enables the collection of regulatory standard data during patient care. FICS brings together traditionally separate and non-communicating applications into a novel, end-to-end platform, paving the way for clinical trials to be done easier, faster, and with great quality. -
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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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secuTrial
interActive Systems
secuTrial® is a professional, entirely browser-based GCP-compliant EDC system for collecting patient data in clinical or non-interventional studies and patient registries. Since the year 2000, secuTrial® has been used in over 600 national and international studies and long-term projects conducted by university institutions, CROs, med-tech manufacturers and pharmaceutical companies – a clear testimony to its superior product quality, universal applications and high customer satisfaction. secuTrial® is a powerful, web-based software solution for clinical trials. It enables patient data for clinical multi-center studies to be collected and managed entirely via the Internet. Full compliance is ensured with all licensing and data privacy regulations while guaranteeing the highest quality standards. -
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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. -
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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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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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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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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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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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DatStat
DatStat
DatStat’s cloud based platform puts the patient at the center, whether at the center of care, or the center the next big clinical trial. Our platform is helping clinicians and researchers engage, empower, and connect with patients like never before. DatStat clinical trial and clinical care solutions are based on our cloud based, patient engagement platform, used by today’s most innovative, leading healthcare organizations. Working closely with customers to understand the specific needs of their department, program, or project, the DatStat team will configure, not hard-code, your solution into our web-based platform. Simply put, we can get your project launched much faster than custom, hard-coded, or paper based solutions, and by putting patients at the center, they get directly involved in the process – improving communication and making your team more effective, all while improving their outcomes. -
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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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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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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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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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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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Dacima Clinical Suite
Dacima Software Inc.
Dacima Clinical Suite is the most advanced web-based solution that combines electronic data capture (EDC), clinical data management software (CDMS), and clinical trial management software in a single platform. Built for clinical trials, epidemiological research, web randomization (IWRS), ePRO, web surveys, and patient registries, Dacima Clinical Suite helps efficiently streamline the clinical data collection process. Dacima Clinical Suite consists of three core modules: Manager (Administrator) Module, Designer Module, and Data Entry Module. -
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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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Saama
Saama
Actionable insights, driven by the industry's #1 AI-powered clinical analytics platform, enable your teams to manage risk and improve performance across studies, systems, sites, and vendors. State-of-the-art clintech from Saama is designed to streamline your workflows, automate time-consuming processes, and improve collaboration across clinical operations, medical review, data management, biostatistics, and pharmacovigilance. Sponsors and CROs rely on Saama for data aggregation and artificial intelligence solutions that lead to better decision-making, eliminate delays, and significantly shrink drug development costs and timelines. Saama can put you on the fast track to clinical trial process innovation. When all your clinical data is in one place and updated in real time, life’s much easier for your ClinOps and medical review teams. Data Managers have been underappreciated for too long. Eliminate manual work so they can pay attention to the data points that matter. -
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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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LARVOL CLIN
LARVOL
The LARVOL CLIN platform delivers comprehensive, AI-powered data intelligence and analytics tailored for oncology and drug-development professionals by aggregating more than 100,000 cancer clinical trials along with detailed results, digitized Kaplan-Meier curves and forest plots, and real-time social-media reactions from over 5,000 oncologists. Users can search by condition, intervention, or trial ID within a single streamlined interface offering expert-curated insights and visual dashboards for data-driven decision-making. The system also covers conference tracking, biomarker and diagnostics databases, and market-intelligence reports from over 25,000 sources, including regulatory communications, clinical-trial registries, and scientific congresses. Built to support pharma and biotech teams in understanding trial outcomes, trends, mechanisms of action, biomarkers, and disease pipelines, the platform integrates deep search filters, heat-maps, real-time alerts, and more. -
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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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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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PharmaPendium
Elsevier
PharmaPendium is a comprehensive resource that provides access to FDA and EMA drug approval documents, including pharmacokinetic, pharmacodynamic, and safety profiles. It offers detailed information on drug-drug interactions, adverse effects, and clinical study outcomes, facilitating informed decision-making in drug development and regulatory submissions. The platform's extensive data supports researchers and healthcare professionals in evaluating drug efficacy and safety, contributing to the advancement of pharmaceutical research and patient care. Find information about previous regulatory submissions and profit from precedents to predict agencies’ requirements. Seamlessly move from table view to interactive charts, graphs, and visual aids to easily interrogate and interpret data. Find information by adverse events (MedDRA), targets, indications, drug,s and endpoints using normalized data. Result pages bridge the preclinical to clinical divide. -
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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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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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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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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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Mahalo Health
Mahalo Health
Mahalo Health is a unified digital health platform designed to accelerate the development of patient-centric digital health applications and clinical trials. By offering prebuilt modules. Mahalo enables rapid deployment of white-label apps tailored to specific therapeutic areas. The platform's unified data capabilities include a predictive health engine for disease prediction and diagnosis, a behavior change engine to promote positive patient actions, and a notification engine for timely communications via push, SMS, or email. Ensuring robust security and compliance, Mahalo adheres to standards like HIPAA, GCP, ISO27001, and GDPR. Its services span various therapeutic areas, including diabetes, cognitive health, cardiovascular conditions, musculoskeletal disorders, mental health, oncology, rare diseases, and nonalcoholic steatohepatitis (NASH).Starting Price: Free -
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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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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. -
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BioGRID
BioGRID
BioGRID is a powerful clinical data tool and visual analytics solution designed to simplify clinical data management and enhance decision-making by combining integrated AI technology with intuitive visualizations, robust compliance tools, and streamlined workflows for clinical trials. It unifies diverse clinical data sources into a single environment, enabling seamless data ingestion, trend analysis, forecasting, and predictive insights that help teams identify patterns and risks while supporting proactive decision-making. BioGRID provides comprehensive study oversight with holistic views of progress and outcomes, automated clean patient tracking, and tools to support efficient medical and statistical reviews. It includes proactive data surveillance and risk-based quality management features that help ensure data accuracy and adherence to industry standards, including tracking of key risk indicators, potential discrepancies, and audit trails.
