Alternatives to TrialStat

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.

In a matter of hours, you can create an eCRF that is just as easy to use and as simple as a paper one. This will help you avoid the most common problems in data collection for Pre-authorisation and post-authorisation studies. When creating an eCRF, make sure you have an EDC that is flexible. This will allow you to adapt to any type of study. The EDC includes a number of monitoring and management tools that will help you save a lot of time and effort in managing and monitoring the study. You should use a valid system that gives trust to the sponsor and allows for the collection of high quality data. Do not wait until the analysis phase to find errors in the data. Otherwise, you will have to chase down investigators to correct them. Avoid making the process of creating an eCRF long and complicated.

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

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

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

Complex eClinical Solutions for EDC/ERT/eCOA significantly speeds up the start and completion of clinical trials (up to 5 days), reduces costs (up to 80% for monitoring), and increases capitalization and attractiveness (recognized by 89% customers). 96% of data science specialists say it increases the knowledge and advancements of Data Management and Data Science professionals. 94% of investigators love interfaces' usability. Strong internal competence in Data Management 365 is an important part of the Data Management 365 policy. This allows us to not only better understand the challenges faced by Data Managers and improve the MainEDC™, but also to transfer technology and best practices to our clients.

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.

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.

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

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

Streamline your clinical studies with Clinvigilant, your global cost-effective eClinical tools provider for CROs, Pharma, Biotech, Nutraceuticals and Academic organizations in clinical and post-marketing stages. Most of our clients choose and stay with us for thanks to our: ♦ Fast EDC set-up (less than 4 weeks). ♦ Cost-effectiveness. ♦ 3rd party integrations (including legacy systems). Our cloud-based suite (Microsoft Azure) is HIPAA, ICH-GCP, GDPR & 21 CFR part 11 compliant and we have been audited by the FDA, EMA and MHRA. The Clinvigilant eClinical suite includes: EDC, CTMS, eCRF, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them within your existing software ecosystem. Every interaction and data exchange creates Audit Trails, which provide compliant real-time data visibility across all relevant roles. Our products are modular, highly customizable, and available on the web, iPad, and Mobile App for both Android and iOS. We also support Patient's Own Device (BYOD) and interface with Devices and Wearables. Clinvigilant💊, your one-stop🌐solutions provider for clinical trials☁️ .

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.

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.

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

Rave EDC (Electronic Data Capture), Medidata's most advanced, robust, and secure EDC system, is used for patient, clinical trial site, and lab data management. Rave EDC is the core of the Medidata ClinicalCloud™, a unified clinical research platform that connects processes and eliminates data reconciliation, and provides cross-functional and cross study data insights. Centrally manage users, roles, studies, sites, and other information across all Rave EDC (and other Medidata Clinical Cloud products). Eliminate duplicate data and inconsistencies in study master data (e.g. different IDs for different sites in different applications). Rave EDC is the core of Medidata's unified solution to Clinical Data Capture and Management. It allows for the aggregation and reconciliation data from multiple sources, Medidata eConsent and Medidata eCOA; and intelligent data review and analysis using Rave TSDV and Medidata Detect.

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.

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

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

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.

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.

Mednet is an eClinical technology company that specializes in healthcare solutions for the global life science community. Mednet's flexible, EDC-centric eClinical platform increases the efficiency of clinical research of all sizes. Mednet's comprehensive solution suite provides all the tools necessary to create and manage clinical research. It can also adapt to changing demands and requirements. Mednet has been trusted by CROs in every sector of the pharmaceutical, medical device, and biotechnology industries for almost 20 years. They provide the expertise, reliability, and innovation that they need to succeed. Mednetsolutions.com has more information.

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

Data management is crucial to the success and efficiency of your clinical research. Despite being complex, Quanta View, an e-CRF, makes it possible to control the processing of your data. Quanta View includes elements such as monitoring, follow up of inclusions, and project management. The application will be there to help you in all aspects of your clinical research. It is accessible via the internet and responsive. It adapts to all media (tablet, laptop, etc.). Quanta view is designed for the pharmaceutical, medical device, and cosmetic industries.

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.

Flex Databases is an innovative, unified, and compliant electronic clinical platform that provides software solutions for clinical trials: pharmaceutical companies and CROs. Our system is composed of: - Clinical Trial Management System - Electronic Trial Master File - Project Management & Budgeting solution specifically designed for the clinical trials industry - Pharmacovigilance System - Learning Management System It was possible to create a flexible platform thanks to our unique experience and a qualified team of more than 100 professionals with a deep understanding the clinical trial process.

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

EvidentIQ's eCOA optimizes real-time, direct from-patient data collection. It offers a simple interface that provides advanced patient assessments to improve the patient experience and data quality. Customers can either benefit from an entire eCOA package, or choose the elements that meet their specific needs to create value. Get a demo from our experts to see how we can help you improve your study ROI. EvidentIQ's eCOA brings together data science and technology. Customers can either benefit from an entire eCOA package that covers all aspects of the process or add value by choosing elements that meet specific requirements. The solution can be used independently of any specific eClinical technologies, such as EDC systems. However, it can be integrated into any existing eClinical software. It has been created to collect any patient/clinician/observer reported outcome data in a streamlined, compliant and efficient way.

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.

Protocol First bridges the physical distance and breaks down silos in Clinical Research during the pandemic. Our solutions can also be used for "normal times". Technology, once a luxury, is now a necessity. We offer the tools you need to stay connected. Not only to help you continue your research but also to speed it up. Remote monitoring and auto-tagging. It can be used with any EDC. Protocol First focuses on breaking down silos between Sponsors, Sites, CROs, and functional areas. We offer comprehensive solutions for the many problems in Clinical Research. Protocol First is focused on getting your data right and to the right places. This includes AI/NLP/ML, both today and in the future. Your data must have an underlying structure. This is the most important aspect of AI. Protocol First's software suite ensures that data from patient to FDA can be used to harness the power of data science.

Data Management is a service we offer. We can help you with data management, statistical analysis planning, and model development. We provide all documentation required by FDA and other regulations. Our past experience has shown that more effort in the planning phase will result in a faster, more efficient trial at the end-phase. Our databases are created by data managers who have worked with many eCRFs and know the essential parts of electronic data capture system design. This allows the eCRF build to be completed in a very short time. Validation and testing of the eCRF is a mandatory part of the design. Different personnel are involved in order to receive a 100-percent detailed eCRF.

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

Cloudbyz EDC, a cloud-native application with an intuitive user interface, is designed to store and effectively manage clinical data throughout the life cycle of a clinical trial. Our innovative solution allows clinical research teams the ability to collect, analyze and manage clinical data that is of varying complexity and size. Create your study without coding, using an interface that allows users to create forms and navigate easily to the appropriate screens for data analysis and collection.

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.

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.

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.

GoResearch™ is a fully validated, innovative internet platform for electronic data capture(EDC) created by 2KMM for research projects such as clinical/observational studies andpatients registries. It supports such projects in many areas, including: configuration of the information flow, the Adverse Events management processes (including automatic e mail notifications to safety departments), random allocation to a treatment arm via the built-in randomization modules, data collection with the use individualized case report forms (eCRF), to meet the requirements for each study, and ePRO and eSource data integration through dedicated mobile and/or Web applications or flexible API (API).

You can jump-start your project with one of our applications. Are you unable to find the information you are looking for? Our intuitive visual designer allows you to create a new app. You can easily create your forms, build workflows, and design your app using our intuitive visual designer. No coding required! Drag-and-drop interface and intuitive visual designer allow you to create your study. The type of study you are doing and the data you want to collect will determine the structure of your database. You can then aggregate and review your data using specialized screens. You can check for discrepancies, manage incomplete forms and track follow-ups. Rediscover your database, and organize it according to the criteria that you choose. Use saved datasets to create filters in natural language for data analysis, workflow planning, patient management, and reporting.

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.

Data collection can be time-consuming and messy for researchers doing clinical research. This is especially true if you use paper forms. Teamscope was created to make it easy for you to collect data, secure it and analyze it instantly. We want you to be less concerned about your research data, and more free to do the things that you love. Teamscope makes it easy to switch from collecting data on paper to electronic in no time. Our online form builder allows you to customize your survey forms with 11 different fields. Skip logic allows you to hide or show fields based on the values entered. Skip logic allows you to create alternative paths and branches within surveys. Each path can be as complicated as you like. Our experts are available to help you create any form on Teamscope.

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

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.

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

Viedoc designs engaging software that modernizes clinical research so that necessary treatments can reach the people who need them faster. We believe in life and science, in people, and in our collective power to change the world and build a healthier future. That unmatched driving force is what pushes us to innovate, accelerate and improve every aspect of modern clinical studies. Since 2003, Viedoc has united scientists and clinical trial professionals in a shared mission of pushing life-changing research forward. Our solution has been used to power thousands of studies, by collecting data from over a million patients and allowing it to flow smoothly across sites and countries. We take great pride in helping bridge the gap between patient and researcher – and, in the best of cases, between research and breakthrough.

TrialMaster, the most intuitive Electronic Data Capture (EDC), Suite on the Market, offers superior usability and flexibility. It is your EDC solution for Phase I to IV clinical trials. TrialMaster increases efficiencies and reduces workflow impact, while improving data quality, which results in faster study submissions. TrialMaster's built-in ePro enables site researchers, patients to self-report their outcomes, and sponsor staff access the platform from any device (desktop or tablet, smart phone, tablet, or laptop). All system screens adjust in real-time to the device's size. Single sign-on (SSO), which allows sponsors to use their own IdP to authenticate, reduces the need for multiple passwords and user names.

Cost-effective data capture. LifeSphere EDC offers sponsors and CROs an economical way to capture, manage, and report clinical research data. It combines disparate systems into one unified database, eliminating the need to reconcile and integrate them. The site captures clinical data directly, eliminating the need to enter data and fill out paper CRFs. Study development time is reduced and changes to live studies can be easily implemented. Integrate with the LifeSphere Clinical cloud platform – including LifeSphere eTMF, LifeSphere EDC – to seamlessly connect operations and data management. Single sign-on functionality allows easy access to a variety of applications. Open architecture allows for rapid integration with third-party applications via API.

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.

CORE (Clinical On Demand Research) offers a range expert services that include the design, construction and running electronic forms for clinical trials in the UK and abroad. CORE not only creates the forms you need but also provides randomization, data management, and all the necessary statistics. CORE provides vital data to researchers in both the academic and commercial worlds. CORE has forged a strong partnership with FormsVision. The Unit first engaged with FormsVision under a FP7 EU funding scheme. CORE has successfully deployed the ALEA eCRF to support trials in the UK and New Zealand. CORE offers a range services, including database build. (CRFs and randomisations, drug supply management, and ePRO (ALEA). Data hosting (ALEA hosting for data/videos/images/documents). Expert advice (including writing a protocol advice, statistics support, and funding application).

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.

Germany is the country with the most research in Europe. Each year, over 600 studies are conducted in clinical and non-clinical settings. It is becoming more difficult to manage and conduct, as is the case with all studies. It is becoming increasingly difficult to coordinate appointments and employees, keep study data up-to-date, and have documents readily available for any queries. You can declare war on the paper economy, exchange heavy files for a tablet and find information in seconds with one click. This will allow you to spend your time doing what is important: research. StudioMED+'s digital study management software will assist you in this. StudioMED+ is a flexible tool that adapts to your needs.

Our application offers a web-based interface that can be used to collect data from a variety clinical situations or study types. The flexibility of the application's data capture methods for collecting patient outcomes allows data to be adapted to any specialty, patient population, research study, or other situation. Improve the quality of patient care by using population analytics and tracking patient-reported outcomes. It is compatible with both personal computers and tablets via a secure web-based interface. Researchers can generate reports in real-time. This allows them to manage the entire process of single-center and multi-center studies regardless of their geographic location. DADOS Platform offers a user interface (UI), and do-it yourself tools for researchers and clinicians to create programs and studies that bridge the gap between clinical care and research. DADOS is easy to use and accessible from anywhere.