Alternatives to Phoenix CTMS
Compare Phoenix CTMS alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to Phoenix CTMS in 2026. Compare features, ratings, user reviews, pricing, and more from Phoenix CTMS competitors and alternatives in order to make an informed decision for your business.
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OpenClinica
OpenClinica
OpenClinica is a leading provider of clinical trial technology, offering a comprehensive suite of solutions to enhance the efficiency and effectiveness of clinical research. The platform provides electronic data capture (EDC), patient recruitment, eConsent, and clinical data management solutions, all designed to streamline workflows and improve data quality. OpenClinica also integrates EHR-to-EDC connectivity, allowing for seamless data acquisition and reducing errors. Trusted by life sciences companies, academic institutions, and government agencies, OpenClinica supports over 15,000 studies and has helped manage data for more than three million patients worldwide. -
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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 -
3
Astracore Clinical Trials
Astracore
Our clinical trials management system is suitable for virtually any controlled clinical trial, including randomized trials, with a choice of randomization algorithms. Clinical trial software is easily configured for paper CRF (Clinical Report Form) and provides eCRFs (electronic CRF). The software can be configured to capture data in a vast number of forms and techniques, with specific rules as defined by you, to build in integrity and quality checking. The system can be used for direct Electronic Data Capture (EDC), i.e. eCRF, or to print paper CRFs which could consequently be entered into the system. You can also attach images, audio, video, documents (say consent forms) etc., limited only by the amount of storage available. The system is Double Data Entry enabled and has detailed exception reporting. This includes and option to lock records once they have been matched, to prevent any further changes. -
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Phoenix PK/PD Platform
Certara
With all the tools you need in a single, interoperable platform, effortlessly share pre-clinical and clinical knowledge across your organization through secure and consistent workflows using Phoenix-based tools and 3rd-party applications. Phoenix WinNonlin is the first choice for non-compartmental analysis (NCA), toxicokinetic modeling, and pharmacokinetic and pharmacodynamic (PK/PD) modeling by over 6,000 researchers at biopharmaceutical companies, academic institutions, and 11 global regulatory agencies, including the US FDA, EMA, PMDA and more. The Phoenix Platform also features population PK/PD (popPK) modeling with Phoenix NLME and Level A correlation via the Phoenix IVIVC Toolkit, Validation Suites provide fast and easy software validation in under 30 minutes. -
5
Phoenix Ortho
Phoenix Ortho
Phoenix Ortho’s software is a comprehensive solution that helps orthopedic surgeons save time while enabling orthopedic clinic administrators to improve operations and medical collections. Phoenix Ortho’s integrated PM software solution helps you submit claims and get paid faster thanks to the PM solution's integrated clearinghouse. Orthopedic practices have specialized needs that multidisciplinary EHRs just don’t fill effectively—causing wasted time and effort. Phoenix Ortho’s comprehensive EHR solution helps orthopedic surgeons save time so they can reclaim their day while helping more patients. Phoenix Ortho circumvents these problems to create a comprehensive EHR system that saves time and improves orthopedic clinic workflows. -
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Transition Technologies eCRF
Transition Technologies Science Sp. z o.o.
Flexible eCRF platform for non-commercial clinical trials, configurable to any clinical trial study protocol. Our eCRF solution was created on the basis of many years of experience of researchers and medical teams with whom we carried out research projects. The system is, above all, easy to use, user-friendly and extremely flexible. The prepared solution meets all the required quality standards, and thanks to the full control over the code, we can further develop and adapt it to the changing requirements of regulators and the clinical trials market.Starting Price: $45k licence -
7
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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QureClinical
Quretec
As a Data Management provider we offer data management and statistical analysis planning and model development with applicable CRF design. All the appropriate documentation is provided by us according to FDA and other regulations. Previous experience has shown us that putting more effort into the planning phase will give a better, faster and efficient result in the end-phase of the trial. Our databases are generated by experienced data managers who have worked with several eCRF-s and already know the critical parts of the electronic data capture system design and data collection. This allows the eCRF to be built in a short period of time. eCRF validation and testing is compulsory part of the design and is dealt by different personnel in order to receive a hundred-percent elaborated eCRF. -
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SimpleTrials
SimpleTrials
SimpleTrials is an on-demand, subscription-based Clinical Trial Management System (CTMS) designed for sponsors, Contract Research Organizations (CROs), and investigative sites. It offers a comprehensive suite of tools to effectively plan, manage, and track clinical study portfolios, including features such as site startup and subject tracking, document management with integrated electronic Trial Master File (eTMF), real-time study analytics, calendar and monitoring, custom fields and trackers, ad-hoc reporting, planning and milestones, site contracts and payments, and electronic visit reports. It supports compliance with 21 CFR Part 11 and provides a secure, validated environment for clinical trial data. Users can customize tracking views, integrate with various Electronic Data Capture (EDC) systems, and utilize built-in templates for consistent document management.Starting Price: $849 per month -
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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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cubeCDMS
CRScube
cubeCDMS is an electronic data capture solution designed for clinical trial operations that streamlines the end-to-end data collection and management workflow. The system supports full data-management workflows including automatic protocol-violation detection, batch query management and native risk-based monitoring to help improve data quality and operational efficiency. The intuitive, no-code user interface enables study teams to build eCRFs (electronic case report forms) from a library of more than 55 ready-to-use forms and edit checks, quickly set up the database, and reduce start-up time. Designed for usability, cubeCDMS allows data entry once and flows data seamlessly across other integrated CRScube modules, reducing redundancy and reconciliation. Additional benefits include AI-powered medical-coding support, drag-and-drop form builders, multi-language support, and robust audit trails and change-history tracking. -
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Greenlight Guru Clinical
Greenlight Guru
Greenlight Guru Clinical is the only electronic data capture (EDC) system built specifically for medical device and diagnostics companies, not adapted from pharma. Designed exclusively for medtech, it combines an easy to use clinical data platform with industry leading customer service, helping teams generate reliable, compliant clinical data under FDA, EU MDR, IVDR, and ISO 14155 requirements. Get a single, validated platform for medical device studies, including: Electronic Data Collection and eCRF ePRO/eCOA (electronic patient and clinician reported outcomes) eConsent Randomization (RTSM) PMCF Surveys (post market clinical follow up) Adverse Events Reporting Open API Used by device manufacturers and medtech CROs running clinical investigations, PMCF studies, registries, and human factors testing. Every customer gets a dedicated customer success manager with real medtech experience and a validation package included with every product update. -
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ClinVigilant
ClinVigilant
Streamline your clinical studies with Clinvigilant, your global cost-effective eClinical tools provider for CROs, Pharma, Biotech, Nutraceuticals and Academic organizations in clinical and post-marketing stages. Most of our clients choose and stay with us for thanks to our: ♦ Fast EDC set-up (less than 4 weeks). ♦ Cost-effectiveness. ♦ 3rd party integrations (including legacy systems). Our cloud-based suite (Microsoft Azure) is HIPAA, ICH-GCP, GDPR & 21 CFR part 11 compliant and we have been audited by the FDA, EMA and MHRA. The Clinvigilant eClinical suite includes: EDC, CTMS, eCRF, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them within your existing software ecosystem. How simple and user-friendly is it? Ask for a demo to find out! Clinvigilant💊, your one-stop 🌐solutions provider for ☁️clinical trials. Enquiries > bd (at) clinvigilant.com -
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AQ Platform
AQ Trials
AQ Platform is clinical research management software for NHS trusts, investigator sites, clinical trials units, site networks, CROs, sponsors and academic research teams. Its modules cover trial management, electronic trial and investigator site files, pharmacy and laboratory workflows, quality management, CAPA, and digital delegation of authority. Shared governed trial records and audit trails connect study operations. Connected Intelligence uses AI to flag gaps and draft next steps; a named user confirms each proposal, and customer data is not used to train models. Hosted in Microsoft Azure UK regions, the platform is designed around ICH E6(R3) and MHRA GCP inspection expectations. AQ Trials holds NHS DSPT Standards Met (2026) and Cyber Essentials certification. Phase 1 trial doctors built it; modules can be deployed individually, and it has been in daily NHS use since 2020. -
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Ofni Clinical
Ofni Systems
Ofni Clinical is a clinical data management tool that rapidly creates and implements secure, regulatory compliant clinical trial databases. Ofni Clinical includes comprehensive search and report features, has strong data validation and edit check options, contains flexible customization tools, and can be implemented quickly and economically. The databases can be used to capture data from existing paper Case Report Forms or as paperless electronic data capture systems. Many Ofni Clinical projects require less than a month to go from project initiation to validated implementation. Contact us today and find out how to use Ofni Clinical for your clinical trials. Matches your existing Case Report Forms (CRFs), reducing training and implementation costs while adding electronic data capture and review capabilities. Includes extensive edit check and data validation features to identify questionable data entry and support data analysis. -
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HEKMA
HEKMA
HEKMA is an AI-powered clinical trial intelligence company focused on accelerating clinical research by improving patient recruitment, trial feasibility, and patient engagement. The company serves CROs, pharmaceutical sponsors, hospitals, and patients through an integrated platform that connects electronic health records (EHRs), AI-driven trial matching, clinical trial management, and patient engagement tools. Its mission is to reduce enrollment delays, improve access to clinical trials; particularly for underserved populations and make clinical research more efficient, transparent, and patient-centric. HEKMA combines expertise in healthcare, artificial intelligence, and clinical operations while maintaining compliance with industry standards such as HIPAA, 21 CFR Part 11, GDPR, and HL7/FHIR. -
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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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ClinSoft
Innovate Research
Innovate’s End-To-End Clinical Data Management Services. Our clinical data management processes, expertise and technology are developed to make each step of your clinical trial data management process more accurate and efficient for Phase I-IV in wide range of therapeutic areas. Our CDM Team Is Well-Versed With Current Good Clinical Data Management Practices (cGCDMP) International conference on harmonization Good Clinical Practices (ICH-GCP) 21 CFR Part 11 Compliance Health Insurance Portability and Accountability Act (HIPAA) Requirements Applicable Regulatory Guidelines SAS datasets SAS XPORT transport files EDC Helpdesk Support 24/7 On-Site and Off-Site Clinical Data Management Services Electronic Data integration and transfer Quality Control Activities Medical Dictionary for Regulatory Activities (MedDRA) Serious Adverse Event (SAE) Reconciliation Clinical Database Transfers Clinical Database Lock paper Case Report Form (pCRF) and electronic Case Report Form. -
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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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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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Calyx
Calyx
At Calyx, we know that the success of your clinical development program comes down to data. Which makes the effectiveness of your electronic data collection (EDC) system key. Used in over 2,600 worldwide clinical trials, Calyx EDC streamlines clinical trial data collection and reporting—in one easy-to-use platform. Don’t trust your important data to just anyone. Contact us to learn how Calyx can propel your program’s success. Calyx EDC gives you the flexibility to easily plan, design, and conduct studies, regardless of their complexity. With features that help reduce costs, improve site visibility, and drive efficiency, Calyx EDC keeps your trial on track. -
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Clinion eTMF
Clinion
Clinion's electronic trial master file (eTMF) system has unique features that simplify storage, access, and management. The simple user interface makes it the go-to tool for clinical trial document management. -
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Clinical Conductor CTMS
Advarra
Clinical Conductor CTMS is a cutting-edge clinical trial management system (CTMS) designed for hospitals, research sites, asset management companies, site networks, health systems, and contract research organizations (CROs). This cloud-based solution helps make the clinical trial process more efficient, thereby helping research organizations make better business decisions and meet every challenge. Key features include electronic data capture, study planning, enrollment management, document management, recruiting management, and more. -
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Arize Phoenix
Arize AI
Phoenix is an open-source observability library designed for experimentation, evaluation, and troubleshooting. It allows AI engineers and data scientists to quickly visualize their data, evaluate performance, track down issues, and export data to improve. Phoenix is built by Arize AI, the company behind the industry-leading AI observability platform, and a set of core contributors. Phoenix works with OpenTelemetry and OpenInference instrumentation. The main Phoenix package is arize-phoenix. We offer several helper packages for specific use cases. Our semantic layer is to add LLM telemetry to OpenTelemetry. Automatically instrumenting popular packages. Phoenix's open-source library supports tracing for AI applications, via manual instrumentation or through integrations with LlamaIndex, Langchain, OpenAI, and others. LLM tracing records the paths taken by requests as they propagate through multiple steps or components of an LLM application.Starting Price: Free -
25
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. -
26
Phoenix
ITB Technologies
Phoenix is the best in the industry end to end product (ERP) for travel agencies and travel management companies. Phoenix consists of fifteen domestic and international suppliers integrated into it with plug and play capabilities. Phoenix is the solution which caters to end to end need for the travel management companies. It eliminating difficulties, or by providing insight to customers via extensive reporting and business intelligence. -
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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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Phoenix Wallet
Phoenix
It is a Bitcoin wallet. It allows you to send and receive bitcoins. At first glance, Phoenix doesn't look different from your typical Bitcoin wallet. The difference is that Phoenix runs natively on Lightning. Phoenix takes care of everything under the hood and you will barely notice anything, except that your payments are faster and cheaper. Phoenix is available for Android on Google Play. Phoenix is available on the AppStore since July 2021. Phoenix is a Bitcoin wallet developed by ACINQ, that allows you to send and receive bitcoins securely over the Lightning Network. It is self-custodial, which means that you hold the keys of the wallet. It provides a simple and clean UX. Thanks to native Lightning support, payments are faster and cheaper. This wallet is self-custodial. Your key, your bitcoins. But make sure you backup your key so you do not lose your money. Do not share your key with anyone. -
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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. -
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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. -
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PRA Prism
Nextrials
Data comes at you from all directions – EDC, EHR, smartphones, mobile devices, central laboratories. Prism assimilates data from these disparate sources and transmutes them into information and ultimately knowledge. Prism EDC combines ease-of-use with innovative features to provide a fresh solution for the collection and management of clinical trial data. Prism offers more that than form-based data collection, it aggregates and manages data from a myriad of data sources. Prism eSource is an innovative software solution that allows research teams to extract clinical trial information directly from a site’s electronic health record (EHR). This creates efficiencies and cost savings beyond the current paradigm where sites must enter the same data in multiple systems and accelerates the delivery of novel therapies to patients. -
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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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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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Phoenix CAD
ProPhoenix
Engineered with Dispatchers in mind, Phoenix CAD is scalable for any size agency: single juris, multi-juris, multi-agency, and multi-site. Phoenix CAD is your solution to manage calls for service for Law Enforcement, Fire, EMS, and OEM/DPW. Our software includes call entry and dispatch functions to get responders to an emergency with all critical information is at their fingertips. This software interfaces with all E911 systems to allow to the automatic entry of the ANI/ALI information in the call-taking screen. ProPhoenix public safety software is an on-premise and cloud-based fully integrated system including CAD, Mobile, Law RMS, Fire RMS, Corrections Management, EMS, Internal Affairs, and Citizen Services. At ProPhoenix, we listen to the ideas of our customers, adopt industry best practices and produce truly superior software applications. We have built our development, support, and implementation teams based on the real-world, the on-the-job experience of our staff.Starting Price: $100000.00/one-time/user -
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Judi
Judi
Judi is a cloud-based clinical-trial collaboration platform built to simplify, secure, and streamline complex workflows across sponsors, CROs, trial sites, and partners. It supports a full range of trial functions, from endpoint/event adjudication, central eligibility review, data-safety-monitoring, remote monitoring, medical imaging, and site/user qualification, to fully custom workflows (Judi Flex). Judi replaces manual processes, spreadsheets, untracked emails, or siloed file-sharing tools with a unified, compliant workspace: every document, communication, image, query, and decision goes through secure, traceable pipelines. Built-in features include role-based permissions, audit trails, real-time chat, query management, dashboards and worklists, flexible document submission and review, eCRFs with edit checks, and reporting tools, making trial data collection, review, and reporting far more efficient and less error-prone. -
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Stenograph Phoenix
Stenograph
Phoenix is Stenograph’s Automatic Speech Recognition (ASR) engine built specifically for the court reporting industry, utilizing Stenograph’s decades of knowledge of legal terminology, formatting, and editing. Phoenix is a powerful tool that allows reporters to become more productive and save time during transcript production, thereby becoming more efficient. Phoenix is being used in CATalyst Check It, which allows stenographers to easily identify mismatches in translation versus the audio, reducing strokes and enabling easy text replacement during editing saving an average of 45 minutes of editing time per job. MAXScribe leverages Phoenix's automatic speech technology and its native legal formatting capabilities to provide a single solution for recording, annotation, real-time translation, editing, and transcript production. Phoenix accuracy in proper nouns, grammar, speaker identification, and question and colloquy identification, provides up to 94% accuracy. -
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Clindex
Fortress Medical Systems
A Clinical Data Management System (CDMS), Clinical Trial Management System (CTMS) and Electronic Data Capture System (EDC) all in one powerful, integrated solution. All your study information can be at your fingertips with our innovative, flexible and compliant Clinical Trial Software System. Our servers or yours. Clindex® can be installed on your servers or it is available on the Fortress Medical Cloud (SaaS – Software as a Service). Cloud access is available world-wide and your data is securely stored at a SOC 3 certified data center. You can build, we can build. Clindex® provides all the tools you need to develop your own study database. Our quick start manuals and help documentation walk you through the process, step by step. Or our Clindex services team can develop a study for you. -
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TrialKit
Crucial Data Solutions
TrialKit is a unified eClinical platform for sponsors, CROs, and research institutions, combining EDC, ePRO/eCOA, eSource, eConsent, RTSM, eTMF, medical coding, imaging, and more in one environment. Floyd, TrialKit's AI model, works directly within the platform to support protocol interpretation, study building, validation, simulation, and analysis. It can generate eCRFs, visit schedules, edit checks, and workflows, while synthetic participants help teams test study configurations. Researchers retain control over reviewing and refining study designs. Web and native mobile apps support data collection across traditional, hybrid, and decentralized studies. Open REST APIs enable integration with external systems, while audit trails and role-based access support study oversight. TrialKit also offers predictable monthly platform pricing without incremental change-order fees for routine study modifications. -
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LabRelations
LabRelations
LabRelations is a modern, configurable laboratory platform built to centralize and streamline scientific and test workflows by combining core modules, including LIMS (Laboratory Information Management System), ELN (Electronic Lab Notebook), CTMS (Clinical Trial Management System) and EDC (Electronic Data Capture), into a single system that supports everything from sample tracking and experiment documentation to study management and regulatory-grade reporting while reducing manual work, errors and data silos; it lets labs store all data in one place, define rule-based workflows and automations, connect instruments and external systems, enforce full audit trails and compliance (such as GxP, 21 CFR and versioned controls), and configure objects, forms, views and permissions to fit specific lab needs, while enabling cross-functional collaboration and real-time visibility from discovery and quality control to clinical research and complex regulated environments. -
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Healthcare solutions from VACAVA reduce the complexity and cost of clinical trial regulatory document management. Each time documents move through a manual workflow, it introduces the opportunity for delays and lost information. VACAVA solutions help you streamline regulatory processes by storing profiles, forms and documents in a single easy-to-access online location. Documents seamlessly move through your workflow with approvals captured electronically (21 CFR Part 11 compliant). Easy-to-read dashboards enable efficient management. VACAVA’s Regulatory Document Management System was built in collaboration with a major clinical trial research base to simplify operations and radically increase efficiency. VACAVA’s Regulatory Document Management System is surprisingly affordable and can be customized to meet your unique needs. VACAVA’s solutions are flexible, scalable, and delivered via the cloud so you never have to worry about managing servers, security, and backups.
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ProPhoenix Law RMS
ProPhoenix
ProPhoenix Law RMS Software starts with our all-inclusive site license giving you the ability to customize the modules you need with access for an unlimited number of users. Developed with 100% browser based technology on the Native. Net framework, ProPhoenix Law RMS allows you to experience a new level of integration, enabling access to your RMS from anywhere, at any time. Phoenix Key Global Information Sharing™ (KGIS) allows all Phoenix users to share data amongst themselves via a secured internet connection to a central location, without duplicating the data. KGIS adopts Global Justice XML standard. Currently, all name and vehicle information, including mug shots and jurisdictional activity for the specific individual or vehicle, is available in KGIS. -
43
Randomize.net
Interrand
Unlimited trial duration, number of subjects, clinical sites, treatment arms and stratification variables, all for a one-time fee. Full support for double-blinded trials, including kit management, kit replacement and emergency unblinding. Randomize.net supports permuted blocked stratification, minimization and simple randomization algorithms. Configure randomization applications with the exact options and features you want. With Randomize.net's Web Service API, you can integrate randomization into your application. Full support for subject randomization and reporting available. Highly secure internet-based randomization service for clinical trials.Starting Price: $2,500 one-time payment -
44
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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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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ClinAccess
MAJARO InfoSystems
ClinAccess™ 5.1 is the next generation of our industry leading Clinical Data Management System based entirely on SAS® 9. It leads the way in simplifying clinical data management, clinical trial analysis and preparation of electronic submissions. Having your data keyed directly into SAS® data sets enhances your staff’s productivity by eliminating the time spent transfering data from Oracle/SQL into SAS. ClinAccess™ is designed expressly for ease-of-use study definition, data entry and management with features to monitor the progress and quality of ongoing clinical trials. Whether for review, analysis, or FDA submission, your data is always in SAS®and ready for analysis. The database structure is designed to support and accelerate statistical analysis and reporting. The result is less time and effort for data analysis and a shorter time to market. For reliability, auditing and security, there is no better solution than ClinAccess™. -
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OnCore
Advarra
Gain visibility into all aspects of your research operations with a comprehensive, proven, and standardized clinical trial management system built through collaboration with leading academic medical centers and cancer centers. Centralize billing designation information to ensure consistency across multiple teams and systems. Improve your budgeting process, route charges correctly, and conduct more accurate auditing/monitoring of billing compliance. Gain visibility and insight into all aspects of clinical research, including comprehensive financial management, with a standardized system built in collaboration with top research institutions. Integrate OnCore with your current EMR, including turnkey interfaces with Epic and Cerner, to increase patient safety, reduce duplicate data entry, enhance billing compliance, and increase operational efficiency. -
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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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Medilake
CLUPEA
Introducing Medilake: Your Premier Solution for Comprehensive Clinical and Non-Clinical Trial Data Management We are delighted to introduce Medilake, an innovative and versatile platform that excels in the seamless management of both clinical trial and non-clinical trial data. In an era where data is the lifeblood of healthcare and research, Medilake emerges as the ultimate choice for simplifying, optimizing, and enhancing data management processes across the spectrum of clinical and non-clinical trials. * Why Choose Medilake for Clinical and Non-Clinical Trial Data Management? - Unified Data Hub - Streamlined Collaboration - Data Integrity and Security - Advanced Analytics - And Scalability and CustomizationStarting Price: $100/month -
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OpenText for Life Sciences
OpenText
OpenText™ Information Management solutions help life sciences organizations leverage insights from data and content to improve decision-making processes and accelerate product development. Integrate, manage, and securely exchange data across people, systems and things. Leverage information assets from R&D to commercialization. Freedom of choice with cloud-native software that can run anywhere. OpenText for life sciences accelerates the discovery process by extracting actionable insights that drive pipeline innovation. Capture and manage research papers into electronic lab notebooks with intelligent capture. Find insights with text mining. Extract knowledge trapped in the unstructured text contained in clinical trial reports, study protocols, clinical safety and efficiency findings. Find out how to intelligently analyze, classify and extract clinical trial documents to reduce the risk of costly stops and starts.
