Alternatives to MEDAS HIMS

ClinCapture's mission is to create software that saves lives. ClinCapture's technology reduces the cost of clinical trials. It streamlines data capture and protects patient privacy. Clincapture is a platform that facilitates the evaluation and development drugs, biologics and devices that have the potential to treat a wide variety of medical conditions or diseases.

Medrio's Electronic Data Capture (EDC) platform and complimenting eClinical solutions such as ePRO, RTSM, eConsent, and Direct Data Capture (DDC) have been trusted by major pharmaceutical, biotech, CRO, animal health, medical device, and diagnostic companies since 2005. We are known for our easy-to-use solutions, delivering speed and simplicity to clinical trials of all phases, sizes, and complexities. Medrio users can build their databases in an average of 2.8 weeks with no programming required, make mid-study changes with just a few clicks of a mouse, and much more. From bolt-on capabilities to full-service offerings, Medrio offers flexible, modular solutions that give our customers exactly what they need – and none of what they don’t. Our innovative software, as well as the robust and flexible training and support resources we provide our customers, have earned us a 98% customer satisfaction rating.

Zelta is a cloud-powered platform for unified clinical data management and acquisition, designed to streamline and enhance clinical trial processes. Its modular architecture adapts to the unique demands of each study, enabling faster and more efficient outcomes. With capabilities such as electronic data capture, clinical operations management—including randomization and trial supply tracking—clinical trial management, and electronic trial master file functionality, Zelta supports comprehensive study oversight. It also enhances patient and provider engagement with electronic clinical outcome assessments and e-consent solutions. Built for studies across all phases, therapeutic areas, and global regions, Zelta offers an intuitive user experience with secure single sign-on access from anywhere. Its flexible and scalable design allows for seamless customization and integration with both native and third-party technologies, ensuring adaptability to diverse research needs.

Dacima Clinical Suite, the most advanced web-based solution, combines electronic data capture (EDC), medical data management software (CDMS) and clinical trial management software into one platform. Dacima Clinical Suite is designed for clinical trials, epidemiological studies, web randomization, ePRO, surveys, and patient registers. Dacima Clinical Suite comprises three core modules: the Manager (Administrator), Designer Module, and the Data Entry Module.

Clinical Conductor CTMS (Clinical Trial Management System) is a cutting-edge system for managing clinical trials. It's suitable for hospitals, research sites and asset management companies. Site networks, health systems, contract research organizations (CROs), and other healthcare facilities. This cloud-based solution makes clinical trials more efficient and helps research organizations make better business decisions. The key features include electronic data capture and enrollment management, document management, recruitment management, and many more.

Clinpal is the first platform for clinical research that is designed to allow virtual, hybrid, and direct-to patient studies. Patients can log in from any device, at any time. The trial's entire life span is managed by study teams that use powerful data and analytics. Sites also have all the functionality they need, which reduces burden. Clinpal Build is a point-and click studio that allows CROs and other users to quickly and easily define data, forms, and workflows. Clinpal's Single Platform provides complete clinical trial support, from patient recruitment through data capture and long-term follow-up. Data is available on-demand. Clinpal's innovative technology - Clinpal can be used in multiple formats with one online configuration. Clinpal works on all devices, including mobile and app users.

HumanFirst is developing the operational infrastructure for distributed care at home and decentralized trials. HumanFirst's workflow management software gives your team and you the tools to allow remote monitoring for your specific needs. Our timeline-based interface supports evaluation, deployment, and management. Atlas contains a list of connected sensor technologies. Physiological and behavioral measures are divided into 150+ categories. There are 25+ therapeutic areas for medical conditions. To sort through the 500,000+ pieces, we used the open-access V3 Framework. Identify technologies that can measure digital endpoints. Remote monitoring can improve patient outcomes. Atlas allows you to share your connected product. Our team is committed to open-access publications and has been featured prominently in peer-reviewed journals. HumanFirst allows home healthcare to be safe, efficient, and equitable.

AI-powered medical image processing meets advanced clinical data automation. UNITY, available as a web-based SaaS solution or on-premises solution, is trusted by major medical equipment manufacturers and hospitals around the world to collect complete, compliant, and consistent data. The integrated modules for PROM and eCRF streamline key data collection to enable faster, more cost-efficient trials. RAYLYTIC’s Imaging Core Lab has decades of experience in high-precision, automated evaluation of musculoskeletal device performance and morphology in spine, hip and knee.

In-system protocol and its training program. Equipted with fingerprint attendance. Cronos offers highly customizable if/workflows that can be used to conduct derma/ patch/ other early phase BA-BE/ phase studies. You can capture, cleanse, and manage your data from paper-based or EDC based trials. Data extraction in desired datasets is possible using standards such as CDISC (SDTM) EDC tool that allows for real-time activities. Its Bedside Data Collection capabilities allow for faster and paperless assessments. It also includes a sample inventory and tracking facility. Compliance-ready data repository.The facility of data e-printing from almost all BA instruments/software and online review of data in defined workflow with e-stamping and e-signature.Project-wise view, export & archival of data. High-quality statistical reports (tables and listings) can be generated in fixed/desired formats.

The industry's best eSource, CTMS and eRegulatory software. CRIO's electronic source is the best in its class and allows you to capture source data instantly and in real time. You can eliminate up to 90% of paper and improve data quality by as much as 80%. CRIO's intuitive clinical trial management system will help you take control of your operations. You can schedule patients, track financials, streamline recruitment, and much more. Electronic regulatory binders are now ready for the 21st Century. This includes the first ever electronic delegation log, all 21 CFR Part 11 compliant. Clinical trial sponsors can now remotely monitor your sites' source data, and regulatory documents via an online portal. Join our network of 500+ clinical research sites from around the world. Our mission is to help your business grow. We help you streamline your site's operations so that your studies don’t stop because you aren’t in the clinic.

TrialStat, in comparison to other EDC tools on the market such as MediData, DataTrack and Omnicomm, is the most comprehensive suite of study management tools. It can seamlessly connect to external data sources like EMR, wearables and other clinical and nonclinical data and information sources. TrialStat is a fully integrated platform that can be used for all types and phases of trials. Our multi-tenant, single-sign-on EDC suite includes modules to randomize, adjudicate, code, safety, patient diaries/ePRO and Vendor Neutral Imaging Archive. It also has a robust Reporting and Analytics Portal and custom Machine Learning programmes. TrialStat focuses on data analytics and provides real-time reporting, data extractions on demand and analytics across a single study or a program. This gives all stakeholders timely, relevant, customized insight into all aspects and highlights areas of risk or potential delays.

5thPort is an eConsent, patient engagement and digital education platform. It can be used in individual practices, hospitals, healthcare systems, and clinical research. The platform uses high-quality, prescriptive media and teach-back in order to educate patients and caregivers about their diagnosis, their care plans, the risks and benefits of recommended treatments, and more. Our digital eConsent helps facilitate a meaningful discussion with your healthcare provider once the patient has been informed. 5thPort can help you achieve the following: 1. Save 15 to 20 Minutes per consultation (without any additional effort) 2. Enhance the patient experience 3. Reduce patient anxiety on the day of their appointments 4. Encourage patients to actively engage in healthcare conversations with their providers 5. Reduce nurse burnout

DatStat's cloud-based platform puts patients at the centre, whether it is at the center for care or at the center for the next clinical trial. Our platform is helping clinicians, researchers, and patients connect like never before. Our cloud-based platform for patient engagement, which is used by today's most innovative and leading healthcare organizations, powers DatStat's clinical trials and clinical care solutions. The DatStat team works closely with customers to understand their specific needs. We will not hard-code your solution, but we will configure it. We can launch your project much faster than custom, paper-based, or hard-coded solutions. Patients are also involved in the process. This improves communication and helps to improve the outcomes of your team.

Clin'form is a flexible and robust electronic Clinical Outcome Assessment platform (eCOA). It was designed to streamline clinical trials, improve data quality and speed up processes for research teams. It is adaptable to any protocol and population, and works with any type of questionnaire. The platform can manage studies with populations ranging from a few to over 10,000 patients in all geographical regions. Clin'form integrates seamlessly with other clinical systems to ensure a smooth workflow. It also supports flexible data collection methods, including provisioned tablet or smartphone, the patient's smartphone, web access via any browser, and interview. The embedded tele-visit function allows for planning the unexpected, and patient engagement modules ensure high compliance.

TrialPoint™, electronic data capture (EDC), is simple to set up and use. Coordinators love it. Our data managers are skilled in converting clinical protocols to geek-speak (metadata dictionary for those in the know). They will set TrialPoint™, so it works for you, and not against you. The system can accept any randomization string or media upload. It can blind users to treatment assignments. To promote time-sensitive data collection. The system will calculate visit windows and send reminders to keep the team on track. Many protocols are now being implemented in trial designs that include patient-reported outcomes on health and quality of life questionnaires. TrialPoint's electronic patient outcomes (ePRO), which can be configured to suit any quality of life questionnaire, patient diary, or other criteria, is worth a look.

DFnet, a healthcare technology company, provides eClinical services, including electronic data capture, eSource and data management services. Our services offer greater flexibility, better data quality, as well as greater efficiency for clinical trials around the world. Collect data from any source, including paper crfs, EDC, other electronic sources, online/offline tablet, and ePRO entries. Install in your secure premises or let us host it in our secure cloud environment. Advanced optical recognition reduces the time required to perform SDV and RBM processes. For multi-center studies with maximum flexibility. Web-based data collection from any source is instantaneously available in a central real-time platform.

AssisTek, a leader in innovative technology solutions for clinical trials, offers custom clinical software to streamline and enhance data collection. Over the past 25 years, they have supported over 800 clinical research studies in 46 therapeutic areas. This includes over 500 multinational Phase I to IV clinical trials. Their eCOA solution is highly scalable, customized, and efficient. It is powered by a proven cloud-based technology platform. AssisTek offers a range of products, including TEK eCOA tablet, which supports any clinical trial questionnaire, TEK eDiary, for capturing patient reported outcomes at home, TEK Configurator, for building clinical trials from the ground up, and TEK Study Portal, for eClinical tracker, training and reports all in one place. Their systems and services make them the number one choice for collection and analysis among patients and clinicians.

Castor is an Electronic Data Capture System for Medical Research. Castor was designed by researchers for researchers. It is easy to use, complete and affordable and offers all the capabilities researchers would expect from an EDC. Top features include self-service eCFR creation (form construction), randomization, patient surveys, monitoring, easy import/export of data, EHR importer (HL7 FHIR-based), audit trails and user management.

EasyTrial.net can be accessed from anywhere because it is a web-based system. EasyTrial.net allows you to easily involve others as you have individual access control which allows you to share data and block access if necessary. EasyTrial.net can be used as a GDPR-compliant storage solution. You have complete control over your data. You are the investigator and EasyTrial.net is the data processor. If requested, they will enter into data handling agreements. We are a specialist in IT and cyber security and are a professional supplier of data security. EasyTrial.net has been used in thousands of clinical trials over the years. This system is approved by many hospitals, data legislation authorities, and educational institutions across many countries.

The options for managing clinical trials at investigator sites were limited to either using multiple spreadsheets or purchasing expensive software that was not suitable for Australian conditions. MAISi is a game-changer. MAISi began as a repository of clinical trials data at a major medical center in 2001. It has since evolved to be a sophisticated workflow application that assists in all aspects of a research unit’s operations. MAISi is a central repository for data that stores information about studies and business units that manage them. The data are organized to support management decision making. Each business unit's staff has access to the data (Studies and Patients, Investigators, Study Teams Members) that is associated with their business unit. Staff granted global access (normally Financial officers and System Administrators) have all data access.

All the power and functionality of a powerful, integrated clinical data management system (CDMS), Clinical Trial Management System(CTMS) or Electronic Data Capture System(EDC). Our innovative, flexible, and compliant Clinical Trial Software System can provide all your study information. Your servers or ours. Clindex®, which can be installed on your server or on the Fortress Medical Cloud (SaaS – Software as a Service), is available. Cloud access is available worldwide and your data is stored in a SOC 3 certified data centre. We can build what you can dream of. Clindex®, provides all the tools necessary to create your own study database. The help documentation and quick start manuals will guide you through each step. Our Clindex services team can also create a study for your company.

Entrypoint is a complete solution for creating, deploying and managing custom data entry applications. It also provides data entry and system administration access from anywhere. Entrypoint offers a range of tools that make it easy to create, deploy, and manage custom data entry applications. It also includes editing, validation, and export options. Entrypoint comes with many built-in attributes which make it easy to add advanced features like range checks and table lookups. Double-entry is the process of collecting information on paper forms and then re-entering it into a computer system. This increases the risk of errors in transcription and takes more time. Electronic forms make it easy to enter data directly into a database without the need for paper. Organizations that are facing rising data volumes and rising costs will find it more appealing to switch to electronic data capture.

ClinOne connects, informs, and empowers participants, care partners, and sites in clinical trials with a true single platform for trial awareness, consent management, and participant experience/retention, underpinned with comprehensive data insights tools and standards-based interoperability. The platform provides solutions such as Site Hub. This is a one-stop-shop for sites to access resources including inclusion/exclusion criterion, site resources and systems landing page. The Connect module contains the Sponsor & Monitor hub, trial awareness, healthcare providers community, site selection and diversity, equity and inclusion data. The Inform module offers consent management, education and eConsent, with eSignature. It also provides data insights and modeling and tele-visit capability. The Empower module provides transportation management, medication monitoring, a caregiver portal and care partner portal.

Most Easy-to-Use Clinical Trial Management System (CTMS) 𝐂𝐥𝐢𝐧𝐢𝐨𝐧 𝐂𝐓𝐌𝐒 integrates seamlessly with Clinion EDC and Clinion RTSM to provide detailed and faster access to the entire trial process to address all aspects of Clinical trial management from a single platform: investigator sites, patients enrollment, SAEs, deviations, inclusions, visit scheduling, IP management, milestones, finances, custom reports, and on-demand analytics enables you to improve quality, control risk, and reduce costs. Clinion CTMS is modular in design These modules are available: Admin Module Project Management Site Monitoring Activities Finance and Budget Management Safety Reporting Management of IP Inventory Document Management System Audit/Activity Log Comprehensive dashboards Comprehensive Reports

Cloudbyz Safety & Pharmacovigilance Solution, a cloud-based solution, is designed to streamline drug safety and pharmacovigilance for pharmaceutical and life sciences companies. The solution automates the process of collecting data, processing it, analyzing it and reporting it in compliance with global regulations. Cloudbyz provides end-to-end management of the pharmacovigilance lifecycle, including adverse event processing, case management, regulatory reporting, signal detection, and risk management. With Cloudbyz, you can optimize your pharmacovigilance processes, accelerate case processing, and increase the accuracy of your safety data, while minimizing risk and ensuring compliance. The benefits of our solution are listed below- 1. Improved Efficiency with Automation 2. Increased data accuracy 3. Real-time visibility 4. Improved Collaboration 5. Enhanced regulatory compliance

Clario CTMS is a user-friendly, intuitive, end-to-end management system for clinical trials. It brings control, efficiency and quality to data flow and workflow. This results in cost savings in time and labor, as well as operational and operational expenses. This web-based CTMS allows you to view and manage your operational performance anywhere and anytime. Clario CTMS, a Microsoft Office-based workplace environment, transforms disjointed clinical trials into a cohesive and efficient work environment by using the most popular office productivity tools around the globe. Clario CTMS can seamlessly exchange information with SharePoint and other Microsoft products. This makes it a powerful, high-performance system. Integrating Office processes with clinical operations can reduce paperwork, significantly lower administrative overhead, and result in a low total cost of ownership.

The premier clinical trial management system, specifically designed to overcome the technical challenges of managing clinical trials. CTMS Master makes it easier for users to communicate, reduces manual work, and eliminates redundant data and tasks. This allows for more efficient trial conduct. A Site Visit Report tool that integrates with an automated workflow eliminates duplicate data entry. It also facilitates the creation and distribution of out-of-the box Site Visit Reports (SVR). Standard templates can be used for site and project documents, budgets, events, milestones and site visit reports. CTMS Master offers more than 100 metrics/statistics to help you track clinical study sites, countries, and projects. It also includes 80+ standard reports and ad-hoc reporting capabilities. CTMS Master allows you to create site-specific budgets using a default template, track accrued and future obligations, and define automatic or manual approval for each payment type.

VACAVA Healthcare Solutions reduces the complexity and costs of regulatory document management for clinical trials. Documents can be lost or delayed if they go through a manual workflow. VACAVA solutions streamline regulatory processes by storing forms, profiles, and documents in one easy-to-access online place. With electronic approvals, documents can seamlessly move through your workflow (21 CFR Part 11 compliant). Easy-to-read dashboards enable efficient management. VACAVA's Regulatory Document Management System was developed in collaboration with a major clinical research base to simplify operations, and dramatically increase efficiency. VACAVA's Regulatory Document Management System can be tailored to your specific needs. It is surprisingly affordable. VACAVA's solutions can be customized to meet your unique needs. They are flexible and scalable and delivered via cloud so that you don't have to worry about security and backups.

uMotif, a modern eCOA/ePRO/eConsent platform, is designed to support clinical and real-world studies. The platform was developed in collaboration with patients and delivers unprecedented engagement, transforming data quality, speed, and accuracy. Combining uMotif’s eCOA/ePRO and continuous glucose monitoring data collection, the platform achieved unprecedented data compliance rates in a pan-European study on diabetes. In an immunology trial, the patient-centered eCOA/ePRO helped the sponsor meet data capture requirements six month earlier. In an FDA-required CNS trial, participants were asked to capture submission-ready data using their own devices. uMotif always puts patients first. They focus on the patient journey, and what drives their behavior. This deep understanding allows for the design of software which best meets the needs and expectations of patients, while also delivering exceptionally high levels engagement to study sponsors.

Research and clinical trials were traditionally conducted outside of local hospitals and doctors' offices. Patients didn't know that research could improve their health or their outcome, and doctors weren't always informed. Elligo allows for a wider participation in clinical research. With access to more than 150 million patients and their data (and more than 150 million others), physicians can offer research as an option to patients who otherwise wouldn’t have access. Traditional methods of recruiting are limited by geographical limitations, such as the proximity of patients to research sites. Patients prefer to work with their trusted healthcare provider.

Signant Health, a global evidence generation company, helps modernize clinical trial by meeting patients where the are and reimagining how to prove. They offer a comprehensive range of clinical technology solutions including electronic Clinical Outcome Assessments, Electronic Data Capture, electronic clinician ratings and a unified eClinical Platform. Their patient engagement tools include a patient app, eConsent and telemedicine capabilities. Signant Health offers clinical data and analytics, including COA data analytics, data aggregation, and intelligence. They have over 30 years' experience and have supported thousands trials and contributed hundreds of drug approvals. This makes them a trusted partner to sponsors and CROs who are looking to deliver high-quality information for trial decisions and regulatory filings.

Science 37 is a company that specializes in clinical research. Its Metasite model eliminates the physical distance as a barrier to participation, allowing patients to participate anywhere. This approach allows access to more than 90% of patients that are not able to participate in site-based research. It offers the recruiting power of twenty sites in one, and provides the flexibility needed by patients to participate from anywhere. The Metasite is powered a proprietary platform which drives uniform study orchestration. It guides the workflow of study staff and patients, and captures study data without requiring manual reentry. This centralization of platforms, people, and processes ensures protocol compliance. It also ensures high-quality data. Science 37's medical teams, telemedicine researchers, and mobile nurses are experienced in conducting remote trials in various therapeutic areas.

Suvoda is a leading clinical trial technology provider specializing in managing complex trials, particularly in areas like oncology, rare diseases, and central nervous system disorders. Established in 2013, the company delivers an integrated platform featuring solutions like Interactive Response Technology (IRT), electronic Consent (eConsent), electronic Clinical Outcome Assessments (eCOA), and ePatient tools. Suvoda’s innovative software ensures streamlined processes for randomization, drug supply management, and real-time patient data collection. Focused on improving patient engagement and simplifying site operations, their solutions are designed to address the increasing challenges of modern clinical trials. With headquarters near Philadelphia and a global presence spanning Europe and Asia, Suvoda has successfully supported over 1,500 trials in more than 85 countries.

TCS ADD platform speeds up speed-to-market for the pharmaceutical industry across all clinical R&D value chains and makes clinical trials more efficient and safer. TCS ADD facilitates digital ecosystems, simplifies data complexity, and provides patients faster access to effective drugs. The platform is powered with TCS Decision FabricTM cognitive artificial intelligence engine, smart analytics and IoT which provides superior business value for the pharmaceutical industry. The next-generation, end-to-end metadata-driven solution for managing industry and sponsor clinical standards. Data science-driven platform that uses AI & ML technologies to speed up study start-up, targeted interventions, and quicker decisions. This solution digitizes the entire clinical supply management process, while placing the patient at the center. This increases patient safety and overall efficacy.

Maximize data quality. Capture eSource data during patient visits to ensure data quality. High-quality data can be electronically captured with built-in validation and edit checks. This reduces errors and queries and allows for remote monitoring. Study time, cost, and risk can be reduced. FDA approved eSource to streamline clinical trials. It eliminates slow, inefficient, and error-prone SDV and transcribing into EDC systems. Streamline study and site efficiency. ez-SourceDocx was designed with site users in view. It streamlines workflows, reduces workload, and ensures protocol execution. It guides sites through properly sequenced visits that guarantee all end points data and prompt quality investigator evaluation.

AcceleTrial™, takes the guesswork out identifying and activating clinical trial sites. Our Study Start-up Management System is based on objective data, not self-identification. AcceleTrial™, a global database of thousands of sites, is indexed and ranked based on: Objective Site-specific Therapeutic Expertise and Objective Site-specific Clinical Test Experience. Objectively match the right sites with objective data on expertise, patient data, and experience to your clinical trials. AcceleTrial™, an automated "push-and-pull" structure, allows you to quickly launch the right sites and begin enrolling patients. It is available in multiple languages. Collect required documents accurately using pre-filled templates. Track activities in real time. You can immediately start using the system - a cloud-based solution that requires minimal IT setup or training. Integrate AcceleTrial™, CTMS, or other clinical trial system.

Deep 6 AI disrupts clinical trial enrollment by changing the way researchers identify eligible patient. DEEP 6 AI uses artificial intelligence and natural-language processing to mine structured and unstructed patient data. This allows DEEP 6 AI to find more patients that are better-matched for trials in a matter of minutes, rather than months. Deep 6 AI is used by some of the most prestigious health systems, pharmaceutical companies, and CROs around the globe. This makes the DEEP 6 platform an essential step in their clinical research workflow, greatly speeding up patients' access to clinical trial. Deep 6 AI locates more patients for clinical trials than it takes months. This allows people to receive life-saving treatments much faster. Deep 6 AI analyzes both structured data such as ICD-10 codes and unstructured clinical information, including doctor's notes and pathology reports. It also provides free-text access to important medical data that cannot be searched easily.

Complion's platform was designed for clinical researchers. Our solution ensures compliance at the highest level with the lowest effort and the most efficiency. This allows you to concentrate on what really matters: improving and advancing patient outcomes. Our eReg solution is available to all clinical trial stakeholders, whether you are a Sponsor, Research Site or CRO. Reduce costs, avoid redundancy and increase staff productivity. You can easily archive, view and get signatures from any device. An audit trail is built into the system to ensure accuracy and eliminate patient safety risks and study conduct. Our clients include hospitals, cancer centers, and medical centers as well as multi-specialty clinics and dedicated research sites.

Our clinical trials management software is compatible with virtually any controlled clinical trial. The software can be configured to generate paper CRFs (Clinical Report Forms) and eCRFs (electronic CFR). Software can be configured to capture data using a variety of techniques and forms. You can also define specific rules to ensure integrity and quality control. The system can also be used to directly capture electronic data (EDC), i.e. eCRF or to print paper CRFs that could be entered into the system. You can attach audio, video, and documents, with the limitations of your storage. The system supports Double Data Entry and provides detailed exception reporting. This allows you to lock records after they have been matched to prevent any further changes.

Koneksa, a leading digital marker company, is a leader in the pharmaceutical and biotechnology industry. They specialize in developing, testing and validating digital markers to help clients understand how their treatments affect patients. Koneksa was founded in 2013 and provides end-toend remote clinical trial assistance, leveraging digital technology, therapeutic expertise, rapid patient-friendly data collection, and remote data collection. This allows for better insights into the health of patients. Their validated, innovative data algorithms are ready for deployment in treatment development programs. This allows the identification of signals sooner and faster than traditional measurements. Koneksa’s cloud-based SaaS Platform allows multiple endpoints be fed in real time, giving immediate data access and empowering confident decisions early in the trial. The platform's ability collect remote data in high volume and with increased frequency allows for ecologically valid measures as well as opportunities to reduce sample sizes.

The Interactive Response Technology (IRT), systems of today are becoming more complex. Flexible and configurable IRT is important - IRT data can be used as the source of record to recruit, drop-out rates in clinical trials, patient visits, or any other vital data. You want a platform that is user-friendly, mobile-ready and comprehensive. It should also be embedded in quality, flexibility, and expertise. In today's risk-based eClinical environment, comfort is combined with complex therapeutic expertise. We empower clinical trials to deliver positive patient outcomes by combining the right technology, subject matter knowledge and a commitment to service. Clients have control over their Randomization and Trial Supply Management processes (RTSM) thanks to deep clinical and supply chain knowledge. Our innovative tools drive exceptional levels of quality control, site efficiency, and patient compliance. Our IRT platform is able to meet the needs for almost any study and allows fully validated deployment in as little time as 30 days.

Lindus Health revolutionizes clinical trials by offering a single solution that delivers faster and more reliable results. Our comprehensive approach integrates CRO capabilities, site operation, and advanced technologies, streamlining all aspects of your study, from design to data collection. We use our in-house technology to expedite the setup of sites and patient recruitment. We also have access to over 30,000,000 electronic health records, which helps us accelerate enrollment. Our pay-on-results model, which is based on a fixed milestone, ensures that incentives are aligned, eliminating delays and unexpected costs. Our clinical operations team, which is responsive and experienced, has an average satisfaction rate of 9.7/10. They are committed to delivering excellence. Lindus Health has expanded rapidly its global presence by conducting over 91 clinical trials in various therapeutic areas including metabolic health and women's health. Diagnostics and medical devices are also included.

Clinion RTSM makes it easy to manage clinical trial supply and patient randomization by using Interactive Response Technologies (IWRS). The Inventory module, which integrates with the Clinion RTSM Software's Randomization module, allows you to implement simple or complex randomization strategies according to protocol specifications. Clinion has one of the best integrated EDC/RTSM platforms available in the industry. Site users can perform Randomization, drug allotment, returns, and re-allotment without having to log in to two systems or worry too much about reconciliation Our predictable and affordable pricing model allows you to lower the cost of RTSM ownership while not sacrificing quality or functionality. You can gain more by integrating EDC and RTSM modules

A comprehensive, proven and standardized clinical trial management system, developed in collaboration with top academic medical centers and cancer centres, will give you visibility into all aspects your research operations. To ensure consistency across different teams and systems, centralize billing designation information. You can improve your budgeting, route charges correctly, and audit/monitoring billing compliance more accurately. With a standard system developed in collaboration with top research institutions, you can gain visibility and insight into all aspects clinical research. Integrate OnCore into your existing EMR, including turnkey interfaces to Epic and Cerner, in order to improve patient safety, reduce duplicate entry, improve billing compliance, and increase operational efficiency.

Data can come at you from many directions - EDC and EHR, smartphones, mobile devices and central laboratories. Prism combines data from many sources and transforms them into information and knowledge. Prism EDC offers a new way to collect and manage clinical trial data. It combines simplicity with innovative features. Prism does more than just collect data via forms. It also aggregates and manages data coming from many sources. Prism eSource, an innovative software solution, allows researchers to extract clinical trial information directly form a site's electronic medical record (EHR). This allows for cost savings and efficiency beyond what is currently possible. It also speeds up the delivery of new therapies to patients.

LexisNexis Health Equity and Inclusion Insights provides comprehensive and actionable data at the individual level on social drivers of healthcare (SDoH). The insights allow healthcare organizations to advance initiatives in population health, health equity, and clinical research. The solution helps identify barriers in care, improve the delivery of care, and create more diverse clinical research and healthcare options. It provides deidentified datasets which can be combined with another deidentified dataset using LexisNexis Gravitas. This tokenization solution leverages a referential layer to match deidentified records with unprecedented precision. To achieve these goals and improve health equity, it is important to identify barriers to health and predictors for poor health outcomes. This will allow targeted action that can make a difference to each patient.

OpenText™, a leading provider of information management solutions for life sciences organizations, helps them to harness insights from data and content to improve their decision-making and accelerate product development. Integrate, manage and securely exchange data between people, systems, and things. Use information assets to drive innovation and commercialization. Cloud-native software can run anywhere, giving you freedom of choice. OpenText for life sciences accelerates discovery by delivering actionable insights that can be used to drive innovation in pipelines. Intelligent capture allows you to capture and manage research papers in electronic lab notebooks. Text mining can help you gain insights. Unstructured text in clinical trial reports, study protocol, clinical safety and efficiency findings, can be used to extract knowledge. Learn how to intelligently analyze and classify clinical trial documents and extract them to reduce the risk for costly stops and starts.

Fusion is Axiom’s proprietary, cost-effective and easy-to-use eClinical solution. It is aimed at small to medium-sized device, pharma and biotech companies. Axiom's Fusion eClinical Suite allows you to add-on any Modules that meet your study needs. Are you running a small study? You can choose the base configuration with EDC and DM, as well as AE/SAE tracking. Are you looking for something more? To make managing your study easier, you can include powerful Modules like Inventory Tracking, RTSM, Safety Management. You can save time by electronically capturing your study data - even offline! Once you have an internet connection, your data will sync to your Fusion databases. Real-time records available for subject screening activities. Fusion Safety Database allows you to manage pharmacovigilance events.

Why is HORIZON ranked among the top 10 LIMS softwares? HORIZON was designed by lab managers and is an affordable LIMS platform that can be configured and integrated with any type of lab. It is not enough to consider a laboratory information management system an afterthought. It is too important to be forgotten. There is a better option. HORIZON LIMS was designed by and for its users. HORIZON is easily integrated and can be configured to adapt to any lab's existing systems. HORIZON was designed to seamlessly integrate with existing workflows, so there is minimal disruption and fast implementation. HORIZON gives you results that you can see right away. A team of problem solvers supports our intuitive interface. HORIZON was developed by lab professionals. We understand what you need in order to deliver results. HORIZON has expert support and implementation teams that will ensure your system runs smoothly into the future.

A simple and powerful CTMS that can be used by hospitals, site management organisations, and small CROs. It focuses on budgeting, financial tracking, and reporting. Clinicubes CTMS has many useful features that allow companies to manage and conduct clinical trials efficiently. The central management of the trial database allows for better productivity and provides more accurate information. Systematize, organize and reorganize the database of physicians and healthcare service providers. A single report will combine data from multiple studies and locations. Reporting options are available to show how the trial is performing against pre-set criteria. Interactive dashboards allow you to communicate study performance data as well as other operational reports.