Alternatives to Lindus Health

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.

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.

We offer a level of collaboration that is not possible in traditional CRO environments. Our goal is to help you succeed in your clinical development program. Clinipace is a global, full service contract research organization (CRO) that focuses on clinical research. Clinipace offers a level of collaboration that is not possible in traditional CRO environments. We place a strong emphasis on personalized services, regulatory expertise, therapeutic leadership, and customized solutions. Our mission is to improve clinical research in major therapeutic areas such as oncology, rare diseases, gastroenterology and nephrology. Clinipace aims to make a difference in drug development and health care. We combine the most advanced technology with a CHALLENGE ACCEPTED approach.

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. The solution benefits are listed below- 1. Secure, reliable & scalable 2. Faster time to value 3. Monitor study progress & risks from planning to close-out 4. Seamless collaboration among sponsors, CROs & sites 5. Improved clinical team efficiency

ClinEdge is changing the clinical trial industry through a comprehensive range of services that are tailored for sponsors, CROs, and sites. Because we understand the problems and barriers our clients face, we can creatively and collaboratively solve them. ClinEdge is committed to increasing overall trial success at every stage of every study. We provide Site and Patient Access for Sponsors/CROs, and enhanced Trial Solutions for Site partners. ClinEdge has over a decade's experience and a deep understanding about our clients and their challenges. We are committed to revolutionizing study conduct.

Study teams are being challenged to do more with less resources. Disconnected systems, manual data entry, redundant workflows and information silos can all lead to delays in a trial's progress. Medidata offers a clinical trial management solution that unites and streamlines workflows, while still maintaining full visibility. Rave CTMS is the only data-driven solution that enables faster, smarter, and more efficient end-to-end trial management. Medidata is an integral part the Medidata Rave Medical CloudTM. It provides all the elements you would expect from an industry-leading CTMS, and more. Rave CTMS gives your study teams the ability to plan and manage clinical trials in a consistent, harmonized way that standardizes activity management and planning at the country, site, and study levels. These activities include the creation and activation of study/site teams, patient enrollment and milestone tracking as well as site monitoring and issue management.

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.

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.

Medable is a software platform that allows you to conduct clinical research and studies. The software actively involves patients, who can be contacted remotely, in order to obtain the best results. Remote consent can be given by patients for digital examinations. The application also adapts to local regulations and languages. Our flexible, modular digital platform and DCT platform allows you to right-size how your protocol will be decentralized. Remote screening at scale worldwide Meet your studies enrollment targets faster. Any screening assessment can be developed. Responsive layouts on mobile and web can improve consent readability. Remote consent can be delivered to patients in a manner similar to consumer digital experiences. Global flexibility and local regulations can be accommodated. Engage patients and reduce the travel and time required for an on-site visit. Increase patient engagement and access.

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.

TrialKit is a cloud-based platform available via both a web and native mobile app, enabling end-to-end clinical trial management for medical device, diagnostics, digital therapeutics, and biopharma companies of all sizes. Design and deploy validated studies in days not weeks using our intuitive study builder that requires no programming. Thousands of global users have leveraged the flexibility of TrialKit to deploy over 8,000 studies across all phases of development.

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.

Ready by ArcheMedX for Pharma and Biotech Trusts to better equip their trial team, improve decision-making, and reduce study delays By understanding which sites and teams are best equipped to conduct the study, you can avoid the most common causes of study delays. Reduce the time and cost of resolving problems, especially early in a trial. You can be confident that the sites you choose truly understand your patient eligibility requirements. You'll feel more confident that they will be better equipped to help you enroll eligible patients faster, meet enrollment targets, and avoid screen failures. You can be confident that the trial team is fully conversant with the protocol, down to the individual and study objectives. You can predict where there are risks so that you can avoid them and have fewer deviations overall.

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.

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.

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.

AI advances will eliminate the need for trial and error in medical practice. Our digital twins allow for confident and rapid clinical trials. We work in neurology, immunology and metabolic disease. TwinRCTs achieve full enrollment faster because they need fewer patients in order to achieve the same power of traditional trial designs. Enrollment time in late-stage trials can be shortened. TwinRCTs increase the power of early-stage studies without adding additional patients, allowing them to observe treatment effects. Early-stage studies can be used to make confident decisions and attract participants. TwinRCTs increase the chances of participants receiving experimental treatments because they use smaller controls groups. Position clinical trials using digital twins to achieve regulatory success. Unlearn engineers the future of medicine using artificial intelligence. We create and deploy new types generative models based on patient-level data.

Calyx understands that data is key to the success of any clinical development program. Your electronic data collection (EDC), system is crucial to your success. Calyx EDC is used in more than 2,600 clinical trials around the world. It streamlines data collection and reporting through one platform. Don't give your sensitive data to anyone. We can help you make your program a success with Calyx. Calyx EDC allows you to plan, design, and carry out studies of any complexity. Calyx EDC helps you keep your trial on track with features that reduce costs, improve site visibility and drive efficiency.

All aspects of your clinical trial can be managed from one platform. Zapclinica, an eClinical suite, is designed to manage and execute every aspect of your hybrid or virtual decentralized clinical trial. Automate complex processes, identify outliers and optimize resources. This will improve decision making and collaboration among sponsors, CROs, sites, and other stakeholders. Zapclinica makes it easier to manage a clinical trial. All aspects of your clinical trial can be managed from one platform. Zapclinica, an eClinical suite, is designed to manage and execute every aspect of your hybrid or virtual decentralized clinical trial. Automate complex processes, identify outliers and optimize resources. This will improve decision making and collaboration among sponsors, CROs, sites, and other stakeholders. Zapclinica makes it easier to conduct a clinical trial that is successful. All aspects of your study can be covered with one platform. You can choose the app that you need in one environment, with no additional vendors or third-party.

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.

ClinSoft™, was developed in-house by Innovate Research. There were no third-party acquisitions and integrations. The system is compliant to FDA regulations (21 CFR Part 11, as well as GCP and HIPAA. The system is fully auditable and validated. ClinSoft™, which is easy to use, ensures quick start-ups and close-outs. This saves you precious time and allows you to be certain that any mid-study amendments or updates to protocols will be made promptly. Innovate Research, an Indian contract research company, provides services in clinical research and regulatory affairs. US FDA 21 CFR Part 11 compliant. Electronic Signatures & Records Secure, Role-Based Access. Audit Trail. Easy to use interface for Edit Checks and CRF Set-up. Frameworks that can be reused for item, panel, visit, and page.

Mosio allows research teams to improve subject adhesion, communications, data collection, and communication on mobile's most popular channel, text messaging. Our software helps research teams communicate more efficiently with participants by delivering interactive elements to mobile phones and messaging automation. WHO CAN WE HELP? + Clinical Trial Sponsors (Pharma & Biotech) + Cancer Centers and Clinical Research Organizations + NIH-Funded Studies + Public Health Agencies + Clinical Trial Managers/Directors and Clinical Operations Managers/Directors. Clinical Project Managers. Principal Investigators. Clinical Research (Study). Coordinators. All research staff who regularly communicate with study participants. BENEFITS + Interactive medication reminders and medication compliance alerts + Automate data collection. + Increase engagement and adherence. + Get SMS appointment reminders to fix your no-show problem. + Increase retention with automated check ins

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

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.

VIPER automates screening from remote patient identification (at point of diagnosis) through to qualified enrollment. VIPER uses artificial intelligence to match patients to precision trials within a narrow window of opportunity. This is done through the ingestion of lab-agnostic genomic and pathology data. It is tailored to the patient and the researcher. VIPER searches the personalized matching engine to locate the best clinical trials available for a patient's specific diagnosis--at that time. VIPER integrates workflow to send real-time notifications to the entire care team about a patient's eligibility in available clinical trials. This is done within a very limited enrollment window. VIPER provides interactive dashboards that allow you to access real-time data mining capabilities to aggregate patient data from both study and site levels to help you reach your study KPIs.

Our cutting-edge platform, the Medidata Clinical Cloud, transforms clinical trial experiences for patients, sponsors and CROs. The Medidata Clinical Cloud is the only unified technology platform that focuses exclusively on clinical research. It addresses every step of the research process, from start to finish. Our platform helps medical device and life science organizations reduce development costs, minimize risks, and bring treatments and devices to market quicker. The Medidata Clinical Cloud will allow you to access the power of any product you choose for your clinical trials program. Medidata is leading the digital transformation in clinical research. Our platform, powered by artificial intelligence, machine-learning, advanced analytics, and advanced research, brings together researchers, study managers and investigators to accelerate research. Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials.

View your study data in real time through a dashboard that allows you to stay up-to date on milestones, progress of the study, and other KRIs. Mitigate risks in research by identifying issues and addressing them as they arise, improving trial performance dramatically. Lokavant's proprietary trial data can be used to optimize resources and reduce the burden on study teams. Trial data is ingested from the source and harmonized with Lokavant proprietary data and data from partners in real-time. Self-service, single view of real-time performance of studies with automated reporting and benchmarking. Daily re-forecasting is used to compare enrollment and site performance against historical performance. This provides actionable insights.

Jeeva's patent-pending modular system is built on the most powerful cloud platform. One login from any browser-enabled device can be used to remotely screen patients, educate, enroll, send SMS, email and generate evidence including electronic patient-reported outcomes. They are tired of waiting for patient recruitment and retention to happen. It is crucial to provide sufficient evidence of safety and efficacy for investigational new medicines in order to receive regulatory agency approval. Jeeva is a great tool for saving time and money for patients, biopharma sponsors, and long-term follow up studies for gene therapy.

eDeviation supports all operations related to Protocol Deviation management and assessment. From software design and validation to gathering supporting documents and exporting data to the TMF, eDeviation®, relieves your clinical staff from the risks of missing or incorrectly assessing protocol deviations.

Arone has over 20 years of experience in software edition and clinical research. We offer clinical research organizations a complete suite to help with patient data entry and management. Our solutions are fully integrated and our team will provide personalized support to help you conduct your studies and projects. All patient data can be managed in one place. Arone manages randomization of patients by randomly assigning treatment options to study participants in order to eliminate bias. Participants in clinical trials can be empowered to enter their data every day. Get a tailored support for your projects.

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.

Korio, the Randomization & Trial Supply Management platform (RTSM), is designed for speed, flexibility, and quality. Not only built to handle clinical trial challenges when they arise, but also built to prevent them from happening in the first place. Korio can handle any trial. Legacy RTSM systems were not designed to support the trend towards increasingly complex study designs. Brittle RTSM systems do not allow for on-the-fly RTSM updates to match changes in clinical trials. Inspired by decades of practical experience. The result is a RTSM platform that combines flexibility with reliability and modernity with experience. Korio's intuitive interface is based on roles and can streamline your user experience. Everyone can work faster and with more confidence, from site users and supply manager to clinical operations and data management. Experience consistent management for your trial.

Choose Curebase to conduct your next study. You will experience more diversity, better enrollment, and better retention. Our innovative approach allows patients to participate at their own homes and with community doctors, resulting in faster, more cost-effective, and more diverse studies. Curebase offers a unique combination: Curebase has in-house virtual CRCs, paired with a global network virtual PIs working with community doctors to bring studies anywhere. Patients don't usually live near traditional research sites. Our trials bring the research into patients' homes, as well as real-world medical settings such community doctors' offices. Patients enrolled in Curebase infectious diseases trials were successful thanks to a new model that meets patients at their location through virtual and community healthcare.

Streamline regulatory operations within your organization to improve compliance. Veeva SiteVault simplifies clinical trial management by connecting all regulatory operations. This improves efficiency and compliance. A single system that integrates regulatory and source documents supports 21 CFR Part 11 compliance and HIPAA requirements. SiteVault Enterprise provides real-time visibility across trials and speeds study activation. It also enables faster and more quality trial execution. To speed up study activation and reduce manual work, you can replace manual processes with your own workflows. Monitors will have secure, direct access into your source and regulatory documents. This will eliminate the need to redact or grant EMR access. You can create your own workflows, reports and dashboards to gain greater insight into regulatory processes and start-up timelines.

Phoenix CTMS is a web application that combines the capabilities of database software used for clinical research in one modular system. The Phoenix CTMS is now publicly available (LGPL 2.0) after years of collaboration with trial sites at Medical University of Graz. This feature set is unrivalled and designed to meet all regulatory and operational requirements of the clinical front end of academic research at CROs (Contract Research Organisations), hospitals and clinics conducting clinical studies at any phase. A CDMS that supports unlimited Javascript form scripting (server-side and browserside) is what you need. You will need to deal with large electronic case report forms (eCRFs) Want to explore an open-source alternative to eCRFs. To create complex queries in ad-hoc databases to find matching candidates using set operations, You will need to conduct multiple trials simultaneously and organize staff and resources at each site. You will need software to implement different processes for ICH GCP.

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.

IQVIA is trusted by thousands of organizations worldwide to accelerate drug development, improve product quality and safety and commercial effectiveness, get the right treatments for patients, improve healthcare delivery and access, and ultimately drive better outcomes. Connect data, technology and analytics to optimize clinical development. The result? The result? Faster decision making and lower risk, so you can deliver life-changing treatments faster. IQVIA offers specialized capabilities to customers in the healthcare industry, thanks to its foundation in data, advanced analytics and expert insights. Watch the latest from IQVIA data scientists and doctors, as well as other subject matter experts, on the topics that are important to you. You can find everything you need, from industry trends to how our capabilities are being applied to help, here.

A global, infinitely scalable, AI powered, collaborative cloud platform that is globally accessible and meets the highest standards for security and compliance. A leading, easy-to-use platform for neuroscience professionals. It was designed by data scientists and neuroimaging experts to meet the unique and challenging needs of the community. Optimized for your specific needs, whether you are conducting clinical trials, designing new algorithms, or leveraging brain-related data.

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.

The industry's best AI-powered clinical analytics platform provides actionable insights that enable your teams to manage risk, improve performance across sites, studies, and vendors. Saama's state-of-the art clintech is designed to streamline workflows, automate tedious processes, and improve collaboration across clinical operations. Saama is trusted by sponsors and CROs for data aggregation, artificial intelligence solutions, and improved decision-making. This can help to reduce drug development costs and timeframes, as well as eliminate delays. Saama can help you get on the fast track for clinical trial process innovation. Your ClinOps and medical review team will find it much easier to access all of your clinical data in one place. Data managers are often undervalued. They can now focus on the data points that are important by eliminating manual work.

Mahalo Health, a unified platform for digital health, is designed to accelerate the creation of patient-centric digital applications and clinical trials. By offering prebuilt modules. Mahalo allows for rapid deployment of white label apps tailored to specific therapeutic fields. The platform's unified capabilities include a predictive engine for disease diagnosis and prediction, a behavior-change engine to encourage positive patient actions, as well as a notification engine that can send timely communications via SMS, email, or push. Mahalo adheres with standards such as HIPAA, GCP ISO27001 and GDPR to ensure robust security and compliance. Its services cover a wide range of therapeutic areas including diabetes, cognitive and cardiovascular health, musculoskeletal disorders (MSK), mental health, oncology and rare diseases.

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.

Secure and user friendly cloud-based EDC platform for managing clinical trials and studies of all sizes and complexities: ePRO, eConsent, eCOA, eSource, PROMs, PREMs, functional health assessments and participant education/engagement.

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.

Clinical One RTSM supports a randomization scheme for the simplest and most complex studies, without the need for programming. This eliminates the need to conduct lengthy user acceptance tests. Self-service configurations allow you to take control of your study and create a study within days, not weeks. Assess the status of drug inventory in real-time and make changes without having to contact the vendor or incurring costs and change requests. Eliminate the need for change requests and avoid delays with quick implementation of changes and promotion of your studies. The only platform to truly unify people, processes and data in order to simplify and accelerate clinical trials for the future. Virtual components in clinical trial allow for greater patient participation, and improve the quality of clinical trial data. To accelerate study start-up, we need to transform digital strategies to harmonize and streamline data from all sources.

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.

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.

A platform that integrates EDC, eConsent and ePRO for efficient clinical trials. Replior is a company that provides software for clinical trials. Trial Online is a suite of software that allows investigators, participants, and wearables to collect and manage data in an efficient and easy way. Trial Online supports decentralized clinical trial (DCT) by allowing trials to operate with remote visits, site visits, or as a hybrid. Our journey began 20 years ago when we were asked to create an online CRF service by one of the largest pharma companies in the world. Back then, we were an IT operations provider for pharma. This was the beginning of software that allows for data collection in clinical trials. Today, we offer a complete suite of data collection software services. Our IT operation is handled by our certified sister company Complior.

Longboat, a cloud-based clinical support solution, provides users with an integrated Guided Compliance toolet to help them at all times. Longboat gives clinical trial staff the resources they need to focus on patients. Longboat allows patients access to essential study information and reminders for their visits. Longboat makes it easy to manage the controlled rollout and revision of the clinical trial protocol.

All-in-one solution for clinical trials using diamond SaaS. Data MATRIX has been working with clinical data since 2009. We analyze data and create documents that can be accepted by the Russian Ministry of Health and FDA. Our products automate clinical trials and allow users to monitor and manage the progress of their projects online. To ensure that the project runs smoothly, we adjust and validate the software before it starts. Our team has completed 180 projects for pharmaceutical and biotech firms and CROs. Six of the 10 top Big Pharma companies have seen their R&D costs drop by 15% using Data MATRIX products. Our employees are proud members of professional groups that include clinical data specialists (CDISC), medical writers (EMWA and AMWA), and data managers (ACDM.SCDM).