Alternatives to Leapcure

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.

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.

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.

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.

Studypages is an integrated clinical trial management system designed to streamline clinical operations and unify participant experiences. It provides a set of tools to facilitate participant engagement, site administration, sponsor oversight, communications, collaboration, and workflow automatization. Studypages integrates these functionalities to create a single platform that increases the efficiency and effectiveness in clinical research. This accelerates the development of new medical innovations.

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.

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.

Ripple, a web-based software solution that allows for the management and recruitment of research participants in clinical, translational, and social science studies is an active registry. Ripple was developed by researchers to transform the participant workflow. It is an end-to–end research participant management system that speeds up the entire research process.

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.

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.

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.

PicnicHealth brings together patients and researchers to provide the most accurate, relevant real-world data. We can create the most comprehensive picture of patient health by working directly with patients, and not just one specialist or care site. With our established patient communities and quick recruitment through dozens if not hundreds of established direct-to patients channels, it is easy to build the right patient cohort. Patients can sign up in just 10 minutes and gain access to their medical records. Are you a part of ongoing trials or registries for patients? PicnicHealth will help you set them up. Our platform provides real-world data tailored to each patient. You can specify the data elements you want to extract from medical records. This includes narrative text, doctors' notes, and more. Patients can contribute more with our unique patient-centric approach to real world data.

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.

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

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.

We create solutions that connect and empower clinical trial ecosystems. The Enrollment Performance Monitoring platform that sponsors love and sites rely on. It is used by over 2,000 research sites in 26 countries, and half of the top-20 global biopharma firms. Sites are able to move patients forward by spending less time on redundant and manual tasks. Sites do less double work. Sites and sponsors will have fewer logs, phone calls, emails, and emails. With real-time access and real-time data, sponsors can optimize enrollment. It is simple and easy to use, with over 1,800 sites in 26 countries using it for patient recruitment. To run more predictable and faster clinical trials, access powerful enrollment and recruitment insights. You can stop wasting time and get back to what matters most: helping patients. You can manage recruitment across all sponsors, trials, and CROs. Once you enter information, it will go where you need.

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.

Our platform provides the comprehensive support your clinical trial requires using cutting-edge cloud-hosted technology. Clinibase will make your organization more efficient and productive. Clinibase is not a plug-and play system. Why? Because every organization is unique and has its own systems and processes. Clinibase can be customized to meet your specific clinical trial requirements. We use surveys to identify areas for improvement and troubleshoot all aspects of your clinical trial processes. Our social integration tools make it easy to quickly locate and recruit eligible participants. Keep your participants engaged by providing smooth communication channels that facilitate high retention and positive participant experiences. Ensure that your trials are valid and safe by storing accurate data.

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.

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.

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.

Clinion eCOA allows you to conduct decentralised clinical trials, with patients participating remotely. Clinion eCOA allows study participant to report their health from their home using their smartphone. This allows clinicians to monitor patients in real time. Clinion eCOA integrates seamlessly with Clinion EDC. Trial participants can input daily outcomes directly. This eliminates data duplication and transcription errors, and provides clinicians with a real time view of patient progress. Multilingual forms are supported by the eCOA app, which makes it easier for patients to engage and provides cleaner data. The eCOA app's decentralised nature allows for faster and wider patient recruitment.

Discover the most innovative approach in the industry to clinical outcomes and data from patient-reported outcome measures. Our robust solution, for example, goes beyond simple data entry and allows a truly patient-centric research study. Our eCOA is based on behavioral science but it was also designed by clinicians in order to meet the needs of sites and sponsors. Personal identity, motivational intervals and meaningful goals. Datacubed's app is easy to use, unlike other eCOA systems. Participants can get straight to the essentials. Our intuitive, flexible and interactive app makes it easier than ever to collect data. We offer data collection in person, remotely or in combination for traditional, hybrid and virtual trials.

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

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.

Effectively monitor clinical trials from start to finish with Ennov’s comprehensive Clinical Trial Management software. Each year, clinical trial sponsors search for new ways to improve the efficiency and reduce the costs associated with running their trials. Investigational site efficiency and productivity can be improved by centralizing information, actively monitoring progress, automating schedules, managing finances, and providing accurate reporting and metrics. With the Ennov CTMS, trial sponsors and CROs are able to actively address all aspects of trial management from a single platform: investigator sites, patients, SAEs, deviations, inclusions, visit reports, phone contacts, investigational product management, trial facilities, and finances. Study managers can plan and track their trials in real time to make better decisions faster. With the Ennov CTMS dashboard functionality, study personnel get on-demand analytics to improve quality, control risk, and reduce costs.

Being organized is key to success in clinical research. It can be difficult to bring the right resources at the right time. This is especially true for document management during clinical trials. GRAVITY is the long-term solution for site and trial master file management. Both files have been converted into an electronic format that is easy to use and coordinates. This package allows for logical and efficient document management. GRAVITY is an integrated eTMF/eISF system. It serves as a portal for sponsors, CROs and Sites. GRAVITY can be used for any entity by itself. Documents begin to flow in when a site has been selected for a clinical trial. However, it is important to maintain the initial pack of essential documents. GRAVITY has unique features that allow users to monitor the essential document management and alert them when documents are about to expire.

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.

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.

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.

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.

Our multi-modal platform is the foundation of everything we do for you and your team. Clinical StudyPal, a patient-centric technology, is fully configurable and comprehensive. It makes your research easier, more efficient, and more cost-effective. It works as an app and encourages collaboration between sites and patients. It acts as a web interface and manages your studies with powerful analytics. It also acts as a notification system, keeping your patients and team informed. What can Clinical StudyPal do? What can Clinical StudyPal do for you? Our team is committed to providing you with everything you need to have a successful trial.

IVR Clinical Concepts is a company that specializes in virtual clinical trial technology. They also offer patient engagement solutions. They offer electronic patient-reported outcome and patient diaries that aim to deliver better results with fewer mistakes, resulting in shorter deadlines and lower cost. They also offer outreach and recruitment services, with a focus on outreach, prescreening, real-time data collection, and data collection in real-time. The screening, registration and randomization solutions they offer are described as being modular, flexible and configurable. IVRCC also offers clinical trial management solutions that reduce workload and provide more control. They also offer eClinical Integration Services to seamlessly connect data. Their chart review services offer real-world data as well as clinical insights. IVRCC focuses on custom, modular and configurable solutions that improve the patient experience while optimizing clinical trial success.

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

Medilake is your premier solution for comprehensive clinical and non-clinical trial data management We are pleased to introduce Medilake, a versatile and innovative platform that excels at the seamless management of clinical trial and nonclinical trial data. Medilake is the best choice to simplify, optimize, and enhance data management processes in an era when data is the lifeblood for healthcare and research. Why choose Medilake to manage clinical and non-clinical trial data? Unified Data Hub - Streamlined collaboration - Data Integrity & Security Advanced Analytics - And Customization and Scalability

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.

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.

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.

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.

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

This company offers a variety of clinical trials management solutions suites for various CROs, Pharmaceutical and Biotech industries. BizNET-CTM is a multi-functional platform that allows a CRO (Contract Research Organization), to plan, manage, design, execute, monitor and analyze trial-related activities and data in compliance with regulatory requirements and protocol obligations. A complete solution suite that addresses all aspects of clinical research projects, from Project Management to feasibility assessment to patient or volunteer enrollment using iris recognition technology to capture clinical trial data and multi-level review to data archiving. BizNET-CTM Suite is designed to manage all documents, tasks and processes, audits, relationships, audits, training, and other information that are required throughout the life of a clinical study.

WCG ClinSphere offers a new approach to running clinical trials from beginning to end. The platform, which uses artificial intelligence to connect sites, sponsors and CROs with participants, is a unified cloud platform. From start to finish, manage your trial from one place. The WCG ClinSphere architecture is based on four principles of efficiency. Our unsurpassed clinical data feeds into a federated AI-learning model, enabling intelligent automation across the lifecycle of clinical trials. Stay informed and make timely decision with access to the latest reports and insights. Workflows that are easy to understand will simplify tasks and improve accuracy. Streamlined operations, logistics, and processes through the entire clinical research journey. The power of massive data stores and deep analysis to make the connections needed for faster clinical research.

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.

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.

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.

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.

Omda MedSciNet improves the quality, utility and management of medical information from collection to analysis. This secure, standardized software allows clinical researchers and other professionals from medicine and academia to easily gather and analyze well managed medical data. The Omda team is specialized in designing and building clinical studies and custom database applications for medical research. The Omda MedSciNet platform is a highly customizable, feature-rich and reliable online environment that hosts and manages sophisticated study and trial systems. Omda MedSciNet is a proven platform that has hosted studies and clinical trial systems of all sizes and scopes for over 20 years. The standard implementation includes all the components needed to establish fully functional clinical trials or studies.

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.

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.

Datatrak International, Inc. is a software-as-a-service provider of enterprise cloud-based technologies for the life sciences industry. Datatrak's unified eClinical solution and related services improve efficiency and cost effectiveness for the clinical trial industry. Datatrak developed its multi-component, comprehensive solution using a single platform. This concept was expanded to include services delivery through Datatrak's Clinical and Consulting Services groups. The Company offers a complete range of software products that can be used to speed up the reporting of clinical research data to sponsors and regulators. This is faster than using loosely integrated technologies. Our goal is to empower workgroups with role-based access, version-controlled file management and calendar events, tasks, and contacts. All built within our eClinical software applications, including EDC, CTMS and reporting.