Alternatives to Unlearn

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.

OpenClinica is a leading provider of clinical data management software solutions. OpenClinica provides powerful tools to ensure that clinical trials are compliant and efficient. OpenClinica Enterprise, OpenClinica Participate and OpenClinica Randomize are the core products.

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.

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.

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.

SimpleCTMS was created to provide the benefits of a CTMS (Clinical Trial Management System) but without the large upfront financial and resource commitments that traditional enterprise systems require or the inefficiencies inherent in worksheet trackers. SimpleCTMS offers early-stage drug developers a cost-effective and scalable solution to improve study startup costs, management, and performance associated with clinical trials. A dedicated client manager offers pro-active support, guidance, and guidance. Our team of clinical software specialists provides technical support to all users. Additional fees may apply for customized training and professional services. Supported by a quality system that uses validated software processes.

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.

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.

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.

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.

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.

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.

Leapcure, a leading platform for patient recruitment and engagement, connects clinical trial sponsors to eligible patients. We use advanced technology and strategies to improve patient outcomes and trial participation. Our platform streamlines recruitment, ensuring that suitable candidates are quickly and efficiently added to trials. Leapcure's mission is to advance medical research by making clinical trial more accessible and efficient. We work closely together with sponsors and patients in order to ensure a smooth and successful experience during the trial. This will ultimately contribute to the development of new therapies and treatments.

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.

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.

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.

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.

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.

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.

Accelerating the development and delivery of life-saving medicines, and enabling cancer patients to have access to the best quality of cancer research and care. Our software revolutionizes patient access to innovative drugs & clinical trials. FICS is a software that allows the collection of regulatory standards data during patient care. FICS combines traditionally separate and noncommunicating applications to create a novel end-to-end platform. This allows clinical trials to be performed faster, easier and with greater quality.

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.

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.

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

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.

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.

Our software provides a complete end-to-end tracking solution that can be used in clinical trials. Simply download the software to your trial managers' mobile devices, and let TruLab's blockchain technology do the rest. To spot potential problems, don't wait for samples to reach a central laboratory. Observe data anomalies as the samples progress through the clinical trial. TruLab allows remote access to samples. 20% of samples are lost in late-stage trials or deemed unusable. This is not acceptable from a logistical, ethical, and financial standpoint. Samples are not collected only at clinical sites anymore. The new world of sample collection at residences presents new challenges in sample tracking. TruLab tracks samples anywhere in the world, from home to repository.

Clinials Trial Search uses AI to simplify complex trial information, increasing participant engagement and enrollment. Benefits: Enhanced Engagement: Empowering participants with plain language descriptions. Access to a diverse group of participants eager to participate in clinical trials. Listing on Clinials trial search is free. Referral fees range from $300 to $5,000 depending on the complexity of the trial.

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.

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.

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.

Formerly eClinicalOS IBM Clinical Development is a unified cloud-based data management platform. It offers a smarter way of collecting and managing clinical data. IBM Clinical Development is a SaaS solution that allows users to access all study data and platform functions via an intuitive and simple web interface.

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.

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.

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.

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.

Our market-leading solution for patient randomization, trial supply management, and patient randomization is available in multiple modalities. It is the most customizable and customizable Interactive Response Technology on the market. IXRS®, which is available in multiple modalities, can accommodate any combination of study objectives. It also includes a team of professionals biostatisticians, integration experts, and language experts that are available 24/7. Site-facing functions are designed for automating steps that are susceptible to human error. Site users can make data corrections themselves without having to call a Help Desk or fear of violating trial compliance. Instead of reading hundreds of pages of legalese and specifications, visual tools are easier to understand. You can view and react to every stage of the software build, eliminating surprises at delivery.

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.

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.

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.

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.

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.

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.

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.

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.

Clinical Ink is your guide to making confident decisions and obtaining cleaner data. Clinical Ink is a pioneer in eSource. Their technology platform and delivery capabilities give you greater certainty from source through submission. Explore Lunexis™, a connected eSource Ecosystem that provides data capture solutions tailored to your protocol at the crucial moments that matter. Lunexis makes it easy to create an integrated, simple eSource solution that gives you access to your study data from anywhere, anytime. We offer more than fast, reliable data. We also provide confidence. Your sites and patients will have a smoother experience. You can also be sure that your patients will be more cooperative and engaged, and that your protocol will be executed correctly. Lunexis can help you make informed, optimal decisions when you start the most complicated studies.

The constructive IWRS ensures a well-organized, systematized supply of drugs between investigation sites. This reduces drug wastage and proactively handles complex randomization procedures for large multi-center studies. SyMetric Platform with Dynamic and Adaptive Randomization helps avoid imbalances between subjects. This results in balanced Treatment Assignment regardless of sample sizes. SyMetric Platform allows patients to handle their subjects. It offers Subject Screening and Enrollment as well as Visit Management, IP dispensing, receipt, Unblinding and Withdrawal tools. This makes it easy and efficient to manage them effectively. SyMetric Platform's robust IP supply management functionality allows drug supply mangers to closely control supplies sent to Sites and adjust supply strategies based on treatment arms and new ratios.

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

eCOA, digital technologies, and other digital technologies, are the future of clinical and research. They bridge the gap between traditional and forward-looking, patient focused development. YPrime's eCOA services are not only high-quality patient data but also provide a better user experience across investigator sites, patients, and sponsors. YPrime uses an agile software development approach to quickly configure and customize functions to meet the needs of each study. This takes between 8-12 weeks. Clients have the opportunity to view the system at various stages of design and development before it goes live. Our pre-validated and configurable authoring environment makes it easy to set up start-up times and make post-production changes such as protocol amendments.

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.