Alternatives to Randomize.net

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.

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.

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.

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

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.

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.

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.

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.

DSG, Inc., a global leader in eClinical, offers a complete suite of innovative technology solutions as well as data management services to the global clinical research community. DSG's eClinical platform offers a competitive advantage and on-time delivery. DSG solutions have been used in thousands clinical trials across the globe using our award-winning eCaseLink™, platform and eCaseLinkDesign for enterprise licensing. The company was founded in 1992 and is proud to have been awarded the SCDM Data Driven Innovation Award.

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 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.

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.

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.

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.

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.

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.

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

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.

Trialpack Designer is a powerful and easy-to-use tool that allows you to create blister packs and cards for clinical trials. It is especially useful for designing packages for complex blinded trials, such as dosage titrations and double-dummy. It contains configuration data for the Trialpack PC Controller and the Trialpack Controlled Dosing Systems. Easy and direct on-screen design of filling patterns, print images, and blister shapes. Access rights for users can be very precise. Workflow features that include electronic signatures. Audit trail that is 21 CFR Part 11 compliant. Reports with detailed packaging instructions.

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.

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.

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.

Cytel is the leading global provider of software for clinical trial design, biometric services and advanced analytics. They specialize in optimizing trials and helping pharmaceutical companies unlock the full potential of real-world and clinical data. Cytel was founded in 1987 by renowned statisticians Cyrus Mehta & Nitin Patel. The company has been at forefront of adaptive trial technology & biostatistical sciences. Our software solutions including the East Horizon platform enable precise trial design and simulation using adaptive and Bayesian methods to optimize protocols and speed up drug development. The East Horizon platform combines key components from Cytel's software portfolio into one unified solution, with R integration. This enhances trial design capabilities. Cytel also offers the Xact suite of software, a comprehensive toolkit that allows statistical analysis of small datasets and sparse or missing data.

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.

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.

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.

Trial leaders can control the timelines and adapt to changing conditions with the eAdjudication®, software managed service. They also have the ability to monitor trends in provider performance over long trials and to ensure protocol conformity. The innovative, all-inclusive managed software service will help you avoid hidden costs and time delays in your Endpoint Adjudication Study. The eAdjudication®, Managed Software Service is the best way to manage Endpoint Adjudication. The eAdjudication® platform allows staff from Ethical, study teams, committee members, and clinical organizations to interact online in real time in a user-friendly and GxP compliant environment. This avoids manual processes that can be costly, time-consuming, expensive, and error-prone. eAdjudication®, all-inclusive services, streamline integration and adoption EA software across eClinical organisations.

Complete control. Full visibility. LifeSphere CTMS is an intuitive trial management system that allows clinical operations teams to reduce complexity, speed up timelines, and stay organized. A modern, user-friendly cloud application streamlines study management and automates key tasks throughout the trial's lifecycle. A simple yet powerful trial management app that gives full oversight of trial activities helps you navigate complexity. Streamline your clinical environment by using a turn-key platform that allows for payments and monitoring, and connects seamlessly with LifeSphere eTMF.

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.

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.

CSAM Studies (previously MedSciNet Studies), is an online environment that allows for secure and highly customizable hosting of clinical trials and studies of all sizes. It has a 20-year history of hosting successful clinical trials and research of all types. Studies is a web-based platform for medical research. It offers a sophisticated online application package that allows you to host, maintain, and monitor projects of any size or complexity. The standard Studies solution from CSAM MedSciNet includes all the components necessary to set up a clinical trial or study. The benchmark solution supports rich and interactive data entry forms, flexible workflow structures, advanced data validation, analysis and exporting capabilities.

RealTime-CTMS (cloud-based clinical trial management software) is a leading, cloud-based system that can be used to increase efficiency and profitability of site networks and research sites. The solution includes fully-integrated services such as RealTime TEXT, RealTime TEXT, or RealTime eDOCS. This allows for faster and easier access to study and subject information through intuitive navigation. RealTime-CTMS also offers other options, including online document storage, appointment reminders and data collection.

Protocol Manager assists clinical operations in managing global trials for drugs, biologics, vaccines and other devices at all stages of development. Protocol Manager will help you comply with FDA's 21 CFR Part 11 regulations by ensuring that your company has implemented the right Standard Operating Procedures. Protocol Manager supports Web Services technology for seamless, automatic integration to many popular EDC or IVRS products. Integration is possible via an export/import method for systems that do not support Web Services. A database and tracking tool that can manage multiple trial information and metrics.

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.

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.

Intrinsic's clinical trials management system (Intrinsic CTMS®,) was designed with the end user's in mind. It minimizes data entry and focuses on proactive study management. Intrinsic is cloud-based and features a simplified interface, the ability of managing studies at any level, as well as a task-based design. This new era in trial management tools has been introduced. Intrinsic®, the first global CTMS, is natively integrated with all Microsoft applications including Outlook, Excel and SharePoint. Users can import bulk data from CROs and study updates using the CRO clinical trial management system. Dynamic Worksheets allows users to quickly create 'live exports' for ad-hoc analysis or reporting. Intrinsic CTMS® also uses Power BI, a cloud-based report tool that allows users to report on data from other clinical system, such as EDC or IRT without having to build expensive data warehouses.

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.

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.

Full cycle product for Research and Development Teams in the Pharmaceutical Industry. The product includes Electronic Trial Master File and Trial Management. It also has Electronic Document Management with eSignature support. This product is suitable for areas regulated by 21CFR Part 11 requirements.

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.

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.

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.

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

The Datimbi Platform is ideal for applications that require large amounts of structured data from many collaborators. It also has built-in quality assurance controls. You can monitor and control the quality of your collection process in real time and perform reporting and analysis. You need to get things set up quickly. Our platform is optimized to handle solutions such as eCRFs in Clinical Trial Management, Social Case Management or any other workflow-driven data collection or processing. You can usually get your platform up and running in one week if your need falls within one of these categories. An easy-to-use web interface allows you to set up roles, workflow transition states, data collection forms, processing rules and lists of values, as well as custom email alerts. These tools can be managed either by your staff or via a Datimbi service.

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.

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.

LifeSphere eTMF provides a single source of truth for your clinical trial. Discover a flexible solution that streamlines the inspection process, ensures compliance and saves time and effort for your organization. LifeSphere eTMF is the first system that supports the TMF reference models. It aligns Clinical documentation, regulations and study protocol in one solution. Create and manage your clinical trial from a single source. Live collaboration and real-time sharing of documents will ensure the quality, timeliness and completeness of your trial master files. TMF inspections can be streamlined quickly and efficiently for any audit. Maintain compliance using embedded workflows and dashboards which allow easy trial reconstruction.

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.

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

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