Alternatives to Beaconcure
Compare Beaconcure alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to Beaconcure in 2026. Compare features, ratings, user reviews, pricing, and more from Beaconcure 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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eKare inSight
eKare
inSight is a comprehensive integrated suite of applications designed to empower researchers with accurate and timely information. The wound assessment and documentation are streamlined with single image capture and synced to a secure HIPAA, GDPR, and 21 CFR Part 11 compliant environment. Create a unified integrated research experience. Leverage emerging data and clinical evidence to develop study protocol, imaging charter, and adjudication manual. Build and configure the database with ease and efficiency. Customize clinical workflow and integrate seamlessly with your EDC. Dedicated project manager to ensure timely start and project maintenance. De-risk your clinical study with the highest quality standards, quality assurance, and control procedures. Analyze data and uncover insights in real time. Curate data sets, and augment clinical studies with real-world evidence. Our wound imaging solution is CE-marked and registered with the FDA. It has been clinically validated.Starting Price: Free -
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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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Ember
MetiStream
Unite and free your unstructured health data Interactive AI and NLP solution delivering health insights to Providers. Payers. Life Sciences. Interactive AI and NLP solution to unlock health insights from unstructured clinical notes data for: Provider. Accelerate data abstraction from and clinical validation of information contained in clinical notes. Decrease time and reduce costs required to identify care gaps, review care quality dashboards, and generate registry reports. Payer. Integrate and analyze both claims data and clinical notes to more effectively manage high risk and high cost member cohorts. Life Sciences. Rapidly match patients to clinical trials–and vice versa–using clinical trial databases and data from clinical notes. Leverage the power of real world clinical data and evidence. Ember is an end-to-end solution at the intersection of NLP and predictive analytics. Streamline. Healthcare Analytics for Unstructured Data to Improve Quality, Efficiency, and Outcomes -
5
Only SAS delivers a single, open, cloud-native statistical computing environment for clinical research with embedded analytic tools, support for data standards, and optional integrated analytic applications. Our analytic foundation for clinical research helps you modernize and deliver new therapies to market faster to improve health. Manage and analyze information in a collaborative platform, streamline processes, and more efficiently deliver trial results to regulatory authorities. Provides a cloud-native, single solution for clinical analysis and submission with everything you need for validation, regulatory compliance, versioning, audit trails, and documentation support. Allows for automation through workflows, support for current and future integrations, and implements and properly manages data standards and controlled terminology. Includes central hub for all incoming data, automated data quality analysis, better data management, and analytical data preparation.
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6
Clindata Cloud
Clinical Data
Clindata Cloud receives pre-clinical / clinical / Risk Metric data from multiple data sources/sites, and empowers the clinical operations teams, with submission-ready data sets, analytics and risk-based monitoring alerts. Consolidate & harmonize study data from multiple data sources into a comprehensive study data model. Validate received data for completeness, accuracy, integrity and consistency and raise alerts and notifications in case of exceptions or risk patterns. Standardize data to CDISC data standards, to eliminate noise and create submission-ready data sets in real-time for continuous validation of data & analysis. Generate submission-ready analytics in real-time based on standardized data. -
7
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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BizNet
Sarjen Systems
Sarjen delivers an AI-enabled Clinical Trial Management System and Bioanalytical LIMS that drives digital transformation across early-phase and late-phase clinical trials. This integrated eClinical platform supports end-to-end trial management, site management, subject tracking, regulatory compliance, and real-time laboratory sample management within a unified ecosystem. Built for pharma, biotech, and CRO organisations, the software enhances operational efficiency through workflow automation, centralised data management, and advanced analytics. Its AI features include predictive enrollment forecasting, risk-based monitoring insights, anomaly detection in lab data, automated query resolution, and intelligent dashboards that improve decision-making. By leveraging machine learning and smart automation, the platform accelerates study timelines, improves data quality, ensures compliance readiness, and transforms clinical research operations!Starting Price: $79 -
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KnowledgeNET
Sarjen Systems
Sarjen's global dossier publishing software is a platform designed to simplify and automate the management and submission of regulatory dossiers. It streamlines the regulatory submission process by automating region-specific and product-specific workflows, which enhances consistency, efficiency, and accuracy. This automation helps to accelerate the creation, validation, and submission of dossiers, reducing manual errors and compliance issues. The solution is built to improve operational efficiency, maintain data consistency, and ensure documentation is audit-ready. By doing so, it saves time and facilitates faster regulatory approvals, ultimately helping to ensure submissions are compliant with various global requirements.Starting Price: $200 -
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Limbic
Limbic
Limbic is a clinical-AI platform tailored for behavioral health providers that enhances patient access, accelerates assessment, and supports therapy using validated, safe AI tools. It embeds into referral pathways to provide Limbic Access, a conversational intake and screening agent that conducts assessments, predicts diagnoses, gauges risk, and generates full clinical reports for clinicians. Limbic also offers Limbic Care, a patient-facing AI companion that delivers guided CBT interventions, conversational check-ins, and between-session support grounded in each patient’s treatment plan. At its core is the Limbic Layer, a proprietary clinical engine that sits between users and a large language model to enforce safety, clinical validity, regulatory compliance, and consistency. The system achieves high diagnostic accuracy and is backed by peer-reviewed research and regulatory clearance, such as Class IIa medical device status. -
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Gesund.ai
Gesund.ai
Gesund is the world’s first compliant AI factory on a mission to help bring clinical-grade AI solutions to market. To help comply with regulatory requirements, our platform audits and validates 3rd party medical AI solutions for safety, effectiveness, and equity. Gesund orchestrates the entire AI/ML lifecycle for all stakeholders by bringing models, data, and experts together in a no-code environment. Standardized, unified, and diversified data customized for your ML needs and regulatory requirements. Gesund.ai assesses model validation needs and provides a suitable mix of high-quality data from its multiple and diverse clinical partner sites. Model owner shares clinical study with Gesund.ai for curation of appropriate dataset(s), and uploads their model onto Gesund.ai's federated validation platform, which resides on hospital premise or private cloud. The model runs against a previously unseen validation data set that has been curated on the hospital side. -
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Docugami
Docugami
Document engineering empowers business users with an impact on day one, without any massive investment in machine learning, staff training, or IT development. Analyze agreements for risk, pricing, and obligations. Avoid costly penalties, and escalators due to delays. Transform carrier plans into data, so your brokers can focus on selling, not data entry. Cut costs, and improve quality vs annual temp staffing. Scour your MSAs and SOWs for deliverables, pricing, liabilities, and legal risk. Avoid expensive surprises. Cut the cost of diligence in transactions. Identify price variations, renewal deadlines, sub-lease options, and tax issues across entire portfolios. Comply with tax laws, optimize rents, and avoid fees. Unlock the data in your unique documents to increase productivity, compliance, and insight. Re-paper legacy licenses to comply with new regulatory and customer requirements. Assure quality reviews and documentation. -
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Flask Data
Flask Data
Flask Data provides life science R&D teams with same-day clinical data and patient safety solutions. The Flaskdata.io cloud API platform unifies data collection apps for patients, researchers, site coordinators, connected devices, and drugs. Our data management and safety monitoring solutions help you reduce risk to clinical data, patient safety, and protocol compliance. The Flaskdata.io platform is automated, scalable, and adaptive to the needs of your clinical trial. Flask Data is a technology company specializing in clinical data management and monitoring. We are accomplished at providing our customers with the most effective way to achieve high-quality clinical data and assure patient safety. There is no single solution that works for every clinical trial. We work hard to understand your unique situation. We work with your team to develop the best solution to achieve high-quality clinical data and assure patient safety. -
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Ennov EDC
Ennov
Clinical data management. A comprehensive solution to capture and manage clinical trial information. CRF creation and intuitive data entry. Support for complex, multi-center studies. Accelerates data validation and processing. Multilingual capabilities. Fit for global deployment, cloud-based or on premise. Every clinical researcher understands the importance of saving time and resources during the conduct of clinical trials. This is especially true when you consider the collection, processing and management of protocol-specific data for each study subject. In the past, study coordinators relied on paper Case Report Forms (CRFs) to ensure the required patient data was recorded and transferred to the sponsor for processing and analysis. Thankfully the days of paper CRFs are largely behind us as the industry understands that the use of electronic data capture (EDC) systems increases the efficiency of data collection and improves overall data quality. -
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Basil
Basil Systems
Basil leverages advanced AI and machine learning technologies to dramatically speed access to the vital insights that drive medical product development success. In a single powerful SaaS platform, Basil unlocks intelligence buried in multiple disconnected data sources. So you can make the right decisions faster – accelerating speed to market, optimizing product strategy, driving innovation, and mitigating risks. Become exponentially more efficient at finding insights and answers for your regulatory strategy. Uncover vital, otherwise unavailable in-market quality and surveillance insights, plus trends and analytics. Find, explore, and analyze over 500k trials for an essential understanding of existing clinical evidence. -
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Midas Health Analytics
symplr
Coordinating care, evaluating and demonstrating quality, identifying risks, and monitoring compliance all require data from multiple sources and systems — and all are key to improving the patient and provider experience. Midas Health Analytics improves operational and clinical performance with solutions that manage risk, control cost, and turn data into actionable insights. Track and trend performance over time, proactively manage and mitigate risk, make data-driven decisions amid constant regulatory changes, and elevate and foster a safe care environment for all. Reach unprecedented operational efficiency when evaluating, interpreting, and demonstrating quality of care performance results to stakeholders in today's complex healthcare ecosystem. -
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Jvion
Jvion
Jvion goes beyond traditional predictive analytics, identifying hidden patient risk across various diseases and clinical events and if that risk trajectory can be changed towards a positive outcome. Our prescriptive AI then recommends appropriate action for each patient, taking into account clinical, socioeconomic and behavioral data, in addition to clinically-validated best practices. Armed with this intelligence, healthcare organizations can improve quality, cost, and the overall patient experience. Analyze clinical, socioeconomic, environmental and behavioral data to find hidden health and financial risks. Evaluate modifiable patients and their unique attributes to drive action plans. Provide evidence-based, prioritized, and patient-specific recommendations within existing workflows. The home is the new hospital. Since the pandemic started, home care has seen a renaissance as patients look to avoid care facilities where they could be exposed to Covid-19. -
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SimpleAnalyzer
Simple
SimpleAnalyzer comprehensively audits clinical and financial files, alerting you to problem areas, inconsistencies and negative trends so you can correct errors in real-time. Because MDS analysis automatically takes place prior to submission, you save time and eliminate costly errors. SimpleAnalyzer’s PDPM analytics will help you succeed under the new payment model through optimized ICD-10 coding practices, detailed PDPM comparisons by facility and resident, and customizable PDPM rules. With SimpleAnalyzer, you can proactively spot problems, maximize reimbursement, maintain regulatory compliance, reduce audit risk and improve the overall quality of care.Starting Price: $82 per month -
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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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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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HealthQx
Change Healthcare
Accelerate your value-based initiatives by quickly analyzing and understanding episode costs. Build provider adoption and engagement with data-driven, evidence-based discussions about total episode costs and individual provider practice patterns. Drive cost and quality improvements by targeting variations in care delivery and provider performance. Empower value-based strategies through analytics, providing insights to help guide network optimization and clinical transformation. Identify value-based care opportunities through an analysis of episode costs, leveraging clinically validated episode definitions. Target providers to engage in value-based discussions through an analysis of utilization, costs, and care variations. Leverage episode analytics to help optimize network designs, transform clinical guidelines, and improve consumer engagement. Streamline episode budget creation by defining average episode costs and associated clinical services. -
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ez-SourceDocx
Alpha Clinical Systems
Maximize data quality. Ensure data quality by capturing eSource data directly during the patient visit. With built-in edit and validation checks, users capture high-quality data electronically, dramatically reducing errors and queries—and delivering data for real-time, remote monitoring. Reduce study time, cost and risk. Promoted and endorsed by the FDA to streamline and modernize clinical trials, purpose-built eSource eliminates slow, error-prone and inefficient SDV and transcription into EDC systems. Streamline site, study efficiency. Designed with site users in mind, ez-SourceDocx streamlines workflows, reduces workload and ensures protocol execution by guiding sites through properly sequenced visit procedures that guarantee all end point data and prompt quality investigator evaluation. -
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Kalypso Accel for RIM
Kalypso
Kalypso provides life sciences companies with a cost-effective accelerator for a RIM system implementation - Accel for RIM. The solution enables an integrated platform to effectively manage and track product registrations, accelerate and improve the submissions accuracy, manage global UDI information, and enable efficient product distribution. It consolidates compliance and quality data from various enterprise solutions into a global source of truth for product registrations and tracking to accelerate regulatory submissions. Deployed using modern APIs to aggregate product data, regulatory documentation and submission packages. Pre-configured for rapid implementation with a validated software system. Based on industry-leading RIM practices and implementations. -
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CluePoints
CluePoints
CluePoints is a cloud-based AI-driven risk-based quality management and clinical data oversight platform that leverages advanced statistics, machine learning, and deep learning to improve the integrity, accuracy, and safety of clinical trial data and processes; it provides real-time anomaly detection and centralized statistical monitoring that identifies outliers and data risks traditional methods might miss, enabling teams to manage risks proactively and accelerate issue resolution in line with FDA, EMA, and ICH guidelines. It includes specialized solutions such as Risk-Based Quality Management (RBQM) for real-time risk detection, Medical & Safety Review (MSR) for consolidated review and query workflows, Intelligent Medical Coding to automate consistent clinical coding suggestions, Intelligent Query Detection (IQD) to streamline discrepancy detection, and tools like the Site Profile & Oversight Tool (SPOT) for adaptive site monitoring. -
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Bluenote
Bluenote
Bluenote is an agentic AI software designed to help life sciences companies accelerate their regulatory submissions and documentation workflows, boosting productivity by automating critical tasks with enterprise-grade security and proven accuracy. It generates first drafts of scientific, clinical, and regulatory documents instantly, aligned with templates, standard operating procedures, and global guidelines, with built-in verification and traceability. It includes an AI assistant to refine data presentations, format datasets and tables, write figure captions, and run gap analyses. Bluenote’s workflow builder and specialized agents automate repetitive, multi-step processes so scientists and subject matter experts can focus on innovation, and its search tools let users explore internal datasets quickly to surface insights and reduce duplication. It also offers translation of technical and regulatory content while preserving formatting and glossary use. -
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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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Paces
Paces
Paces is a GIS and data platform accelerating renewable energy project development by de-risking projects from day 1. Its Accelerated Development Framework (ADF) eliminates bottlenecks with AI-driven site vetting, pre-vetted locations, and integrated workflows, cutting timelines and costs while accelerating clean energy deployment to meet rising demand efficiently. It offers market suitability analysis to identify the best markets for unique strategies with tailored recommendations and in-depth analysis of over 155 million sites. Site selection & ranking provides access to pre-vetted, risk-assessed sites in target markets with multi-dimensional data for faster, smarter decisions. Development support includes customized solutions, data verification, and risk assessment to ensure the best projects are presented to the right partners. -
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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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CINCO
Cinco
A web based software that uses Quality Risk Management to organize, analyze and trace Quality information directly to the specific risk it represents to the patient and drug product. Why Us? CINCO, a risk-based quality management software for the Life Sciences Industry. It provides paperless traceability of every critical to quality aspect of a drug or medical device to enable transparent quality decisions at every moment. Why Risk Management? Quality Risk Management is methodology that provides an objective approach into identifying and mitigating the risks of a drug or medical device manufacturing process. It is currently required by most regulatory agencies. However, the paper-based approach the Life Sciences Industry currently uses its ineffective in managing the significant and valuable risk data. It is prone to errors, introduces too much friction to the users and ends up not adding the potential value to the operations. On-demand access to what is critical to the product qua -
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Iguazio
Iguazio (Acquired by McKinsey)
The Iguazio AI platform operationalizes and de-risks ML & GenAI applications at scale. Implement AI effectively and responsibly in your live business environments. Orchestrate and automate your AI pipelines, establish guardrails to address risk and regulation challenges, deploy your applications anywhere, and turn your AI projects into real business impact. - Operationalize Your GenAI Applications: Go from POC to a live application in production, cutting costs and time-to-market with efficient scaling, resource optimization, automation and data management applying MLOps principles. - De-Risk and Protect with GenAI Guardrails: Monitor applications in production to ensure compliance and reduce risk of data privacy breaches, bias, AI hallucinations and IP infringements. -
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Clario eCOA
Clario
Unlock better evidence with high-quality ePRO and eClinRO. Electronic Clinical Outcome Assessments, or eCOA, measure how patients feel or function during clinical trials. By capturing clinical data electronically, you can be confident that your patient’s data is high-quality and regulatory-compliant. Put simply, eCOA avoids the quality and time issues associated with paper diaries, such as illegible answers, transcription errors and inconsistent or conflicting data. Also, the FDA recommends ePRO. Patient-reported outcomes, patients report on their health via questionnaires or assessments. Examples include quality of life or activity outcomes. The clinician reported outcomes. Health outcomes are reported by a clinician. An example may include a physical examination such as PASI. Performance outcomes are measures from specific tasks the patient is asked to perform. An example might be performing a timed task. -
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WinWire Vaccine Management
WinWire Technologies
Digitization of vaccine administration and distribution. Public health administrators, communities and healthcare providers look for a robust and adaptive COVID-19 vaccine management solution that will expedite vaccine deployment securely and equitably. WinWire’s Vaccine Management Solution enables health officials and providers to manage vaccine distribution, expedite vaccine administration, citizen registrations, and simplify monitoring. It provides rapid deployment, easy integration with EMR & IIS. It also automates back-end supply-chain clinical processes and inventory management & enables patient service quality improvement using a secure healthcare data. This data-driven digital solution is able to handle vaccine planning and delivery in a pre-integrated, fully customized, or standalone mode with a laser-focus in providing web-scale, easy-to-deploy, intelligent systems. Rapid Deployment Highly configurable deployed in 2–3 weeks. -
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Agatha
Agatha
Agatha offers a suite of cloud-based applications tailored to the life sciences industry, enabling centralized management of documents and processes across clinical operations, quality, regulatory, and training functions. It supports biotech, pharmaceutical, medical-device, and contract-research-organization workflows by offering modules such as eTMF (Inspection-Ready Master Trial File), Remote ISF (Investigator Site File) management, SOP creation and approval, Quality document management for CAPAs, deviations, and change controls, and regulatory document management. Agatha enables streamlined document creation, review, approval, storage, and sharing in one unified system, supports paperless transformation to reduce administrative burden and strengthen data security, and is built on a global-compliance architecture addressing standards like 21 CFR Part 11, GDPR, and EU Annex 11. -
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Oncora
Oncora Medical
Improving the quality of care and outcomes for cancer patients requires collaboration between physicians, scientists, cancer centers, and patients. Oncora's intuitive software platform allows all stakeholders to capture and apply real-world data for all healthcare-related decisions, for the benefit of the patient. Our products are built for healthcare professionals dedicated to improving cancer outcomes. Simplify workflow, reduce documentation burden, and optimize treatment with intelligent patient care software. Capture and visualize regulatory-grade real-world data with intuitive and dynamic software tools. Measure quality and streamline operations to improve care with advanced reporting tools. Rigorous clinical research with top cancer care professionals. Intuitive, web-based software to power your cancer center. Data and software to accelerate clinical discoveries. -
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eDeviation
eDeviation
eDeviation supports all the operations for Protocol Deviation assessment and management. From software design and validation to collecting supporting documents and exporting data for the TMF, eDeviation® relieves your clinical team from the risks associated with missing or wrongly assessing one-time or recurring protocol deviations. eDeviation® is part of Ethical’s eClinical Software Platforms Solutions supporting faster and more accurate clinical trials management. Whether your protocol deviation assessments are performed by an independent expert committee or by your study team, our eDeviation® software is configured to exactly match your needs. Forms, workflows and exports altogether contribute to a GxP quality and effectively managed study. Study teams, Investigators’ Sites and Committee Members, when applicable, work seamlessly online in real-time to expedite judgments, consensus and timely completion of the protocol deviation assessments and management. -
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Clinion EDC
Clinion
AI-enabled and Integrated Electronic Data Capture (EDC) Software Clinion EDC is the most Integrated Electronic Data Capture System in the Industry making your clinical trials faster and better. Our Electronic Data Capture(EDC) Software accelerates the speed of your clinical trial by reducing deployment time, capturing data faster, timely study close-out, and early data lock – all in a cost-effective manner providing the highest data quality, integrity, and security. Clinion EDC Software integrates all the functionalities you need into one platform, from study setup to data management and reporting. What can you expect? - Quick mid-study changes, no need to rely on tech support or take your study offline. - Accelerates data validation and processing by using form rules like edit checks and skip logic. - Support for complex, multi-center studies - Can be integrated with Clinion RTSM, Clinion eCOA, and Clinion CTMS - easy-to-use interface and AI-enabled features -
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SteadyMD
SteadyMD
SteadyMD is a telehealth infrastructure and clinical care platform that powers high-quality virtual healthcare experiences for patients and healthcare organizations across all 50 U.S. states by providing an on-demand, technology-enabled clinician workforce, clinical operations, legal/regulatory support, and secure telehealth technology. It offers a broad spectrum of care services, including primary care, urgent care, chronic and condition-specific care, therapy, lab order review, prescription approval, and personalized treatment plans delivered via video, phone, or asynchronous messaging, enabling seamless patient interactions without in-person visits. SteadyMD includes tools such as Telehealth APIs, a white-label telehealth platform, and the SteadyMD Digital Clinic that integrate with partners’ systems, support intake forms and scheduling, and route consults to clinicians licensed in the patient’s state while maintaining HIPAA-compliant security. -
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Custovia
Custovia
Custovia AI is an AI-powered customer intelligence platform that generates hyper-realistic synthetic customer personas from your own data to help teams test products, features, and marketing campaigns before launch by simulating how real audiences think, behave, and respond, accelerating insights from weeks to hours while keeping data secure and privacy-first. It distinguishes itself from traditional persona methods by building dynamic AI personas continuously updated from real behavioral data rather than static assumptions, enabling companies to validate ideas, de-risk decisions, and refine strategies quickly without the high cost and delays of conventional research. Custovia offers a ready-to-use library of AI persona types and lets teams connect their own data securely to create custom personas specific to their audience and products, then set up experiments and learn instantly from simulated responses across segments.Starting Price: Free -
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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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Loftware Cloud Clinical Trials
Loftware
Loftware Cloud Clinical Trials is a comprehensive labeling and booklet management solution designed for the clinical trials industry. This platform helps streamline the creation, approval, and distribution of clinical trial labels, ensuring strict compliance with regulatory requirements such as FDA, EMA, and ICH. Loftware offers a centralized solution that manages labeling operations across global clinical trials, reducing errors, ensuring consistency, and improving overall efficiency. The software supports customizable templates, barcode generation, and integration with other systems to provide a seamless workflow throughout the clinical trial process. -
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DNAnexus Apollo
DNAnexus
DNAnexus Apollo™ accelerates precision drug discovery by unlocking the power of collaboration to draw critical insights from omics data. Precision drug discovery requires collecting and analyzing huge volumes of omics and clinical data. These datasets are incredibly rich resources, but most legacy and home-grown informatics tools can't cope with their size and complexity. Precision medicine programs can also be hampered by siloed data sources, underpowered collaboration tools, and the burden of complex and always changing regulatory and security requirements. DNAnexus Apollo™ supports precision drug discovery programs by empowering scientists and clinicians to explore and analyze omics and clinical data together, in a single environment, built on a robust, scalable cloud platform. Apollo lets them share data, tools, and analyses easily and securely with peers and collaborators everywhere - whether they're on another floor, or another continent. -
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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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eHana EHR
eHana
One client, one record. Capture and share data across your entire continuum of care with no duplication of effort and no paper. Slice and dice data, plan strategically, provide more informed care, and "wow" your referral sources and auditors. More timely and accurate data captured and validated in real-time means fewer errors and faster processing time. With eHana EHR, your team can be more productive and focus on what matters most, providing high quality and sustainable clinical outcomes. Integrated multi-program client demographics and clinical record. Support for a broad range of program types and services. Flexible security configuration for clinical records. Electronic signatures for clinical documentation. Incident logging and reporting. Integrated e-Prescribing. Integrated data model to eliminate redundant data entry. Client and employee scheduling and practice management. -
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Brellium
Brellium
Brellium is an AI-powered clinical compliance platform designed to audit clinical documentation, billing, and payor risk across every patient visit. Its core capabilities include real-time chart review using machine learning to check every note, session, and encounter for coding compliance (MDM/E/M/ICD-10), clinical quality standards, payor rules, and documentation integrity, delivering audits up to 13x faster and reducing chart-review costs by approximately 98%. Brellium integrates with any EMR, supports custom and prebuilt audit criteria, sends automatic provider-feedback emails, and provides trend-data dashboards that stack-rank clinicians based on documentation quality. It also offers a unique clawback-protection guarantee: if a payor retracts reimbursement on a Brellium-approved chart, Brellium will cover the cost. The platform serves specialties such as behavioral health, ABA, home health, chronic-care management, and telehealth. -
45
BIOiSIM
VERISIMLife
BIOiSIMTM is a first-in-class 'virtual drug development engine' that offers unprecedented value for the drug development industry by narrowing down the number of drug compounds that offer anticipated value for the treatment or cure of specific illnesses or diseases. We offer a range of translational-based solutions, customized for your pre-clinical and clinical programs. These offerings are all centered around our proven and validated BIOiSIMTM platform for small molecules, large molecules, and viruses. Our models are built on data from thousands of compounds across 7 species, leading to robustness rarely seen in the industry. With a focus on human outcomes, the platform has at its core a translatability engine that transforms insights across species. The BIOiSIMTM platform can be used before the preclinical animal trial start, allowing earlier insights and savings in expensive outsourced experimentation. -
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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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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. -
48
Clootrack
Clootrack
Clootrack is an AI Superagent for Fastest Customer Intelligence. It gives access to actionable customer and market insights 7.5X faster, with both qualitative and quantitative analytics. It helps enterprises uncover the exact reasons behind customer sentiment, which is used to enhance overall customer experience, reduce customer churn, accelerate product development, and enter new markets. The insights are based on a comprehensive set of data, both first-party and online. Clootrack insights, including qualitative data, are 98% accurate. Our patented unsupervised analysis ensures qualitative insights are unbiased and actionable. The platform includes 1000+ connectors to enterprise data sources and can crawl data from online sources. -
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ClinicPlus
TRM NETT Systems
ClinicPlus is a Complete Clinic Software. It covers the complete workflow a GP (General Practitioner) and Specialist Clinics. This user-friendly yet comprehensive software solution will save a tremendous amount of workload for the clinics. With this great tool, clinics can drastically reduce the administration and management hassle and dedicate their time to providing quality healthcare services. Without proper control on cash collection, drugs inventory & claims submission (billing) any medical practice can lose substantial income based on services rendered. Suitable for factories, organizations with more than 500 employees, colleges and universities. Cost-effective & reliable communication medium between clinics and the management office. One platform for in-house clinics and panel clinics outside the organization. -
50
Lionbridge
Lionbridge
Remove inefficiency, complexity, and manual repetitive tasks from your localization process with the all-in-one Lionbridge Translation Management Platform, where you can automate your workflow, track your tasks, and view project status updates in a central online portal for all your translation projects. To translate your highly regulated content, you need to ensure it satisfies regulatory requirements and resonates with your global readers. Whether you need legal translation services, financial translation services, or translation services for the life sciences industry, Lionbridge can help. Our clinical trial translation services teams translate the full range of documents related to clinical trials, whether they contain scientific, medical, legal, or plain language content. We translate and validate primary, secondary, and tertiary labels for investigational drugs, placebo, comparator drugs, or auxiliary medicinal drugs used for clinical protocol endpoints.
