Alternatives to KLINDAT

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.

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.

In-system protocol and its training program. Equipted with fingerprint attendance. Cronos offers highly customizable if/workflows that can be used to conduct derma/ patch/ other early phase BA-BE/ phase studies. You can capture, cleanse, and manage your data from paper-based or EDC based trials. Data extraction in desired datasets is possible using standards such as CDISC (SDTM) EDC tool that allows for real-time activities. Its Bedside Data Collection capabilities allow for faster and paperless assessments. It also includes a sample inventory and tracking facility. Compliance-ready data repository.The facility of data e-printing from almost all BA instruments/software and online review of data in defined workflow with e-stamping and e-signature.Project-wise view, export & archival of data. High-quality statistical reports (tables and listings) can be generated in fixed/desired formats.

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.

Check out our quick screening tools to help you identify high-risk patients with colorectal, breast and other cancers. Progeny Clinical makes it easy to manage family history, assess risk, and determine treatment options for your patients. You can access family history data online from your patients and create pedigrees automatically before you visit the clinic. You can edit or create new pedigrees at any time. You can instantly run validated hereditary risk assessment models for cancer at the touch of one button. Ambry Genetics offers genetic testing at a fraction of the cost. You can track and view lab results without leaving the software. Save time by creating letters, notes, reports, letters, and other documents using custom templates that include patient data fields. Quickly generate custom queries or spreadsheet reports using pre-configured data entry screens. To display the most recent pedigree, add a hyperlink to your electronic medical record.

ClinAccess™, 5.1 is the next generation in our industry-leading Clinical Data Management System, based entirely upon SAS®. It simplifies clinical data management, clinical trial analysis, and electronic submissions. Your staff will be more productive if your data is directly linked into SAS®. This eliminates the need to transfer data from Oracle/SQL into SAS. ClinAccess™, which is specifically designed for ease-of use, data entry, and management, includes features to monitor and track the quality and progress of ongoing clinical trials. Your data is always available in SAS®, ready for analysis, review, and submission to FDA. The database structure was designed to facilitate and accelerate statistical analysis. This results in less time and effort to analyze data and a shorter time to market. ClinAccess™ is the best solution for security, auditing, and reliability.

Electronic source documents - eSource – eliminate paper, standardize and simplify workflow and reduce errors and omissions. BREEZE eSource does more than just schedule visits and create templates. BREEZE eSource synchronizes clinical contexts, regulatory requirements, and protocol requirements with study procedures. This ensures that users capture all protocol-required data. BREEZE business rules ensure that data collected is accurate, complete, accurate, and in compliance with regulations. Our dedicated team of clinical trial specialists delivers customized, study-specific eSource documents to review and approve before study start-up. They also support you throughout the trial by modifying them as necessary. Modules work seamlessly together. Cross-Module Action Multiplier takes things one step further, anticipating and completing automatically any additional tasks you enter. For example, the completion of visits or procedures automatically posts invoicing, recalculates scheduling, etc.

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.

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.

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.

EasyTrial.net can be accessed from anywhere because it is a web-based system. EasyTrial.net allows you to easily involve others as you have individual access control which allows you to share data and block access if necessary. EasyTrial.net can be used as a GDPR-compliant storage solution. You have complete control over your data. You are the investigator and EasyTrial.net is the data processor. If requested, they will enter into data handling agreements. We are a specialist in IT and cyber security and are a professional supplier of data security. EasyTrial.net has been used in thousands of clinical trials over the years. This system is approved by many hospitals, data legislation authorities, and educational institutions across many countries.

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.

Catalyst ABA Data Collection. Catalyst can be used to collect and manage a variety of data types. Your Catalyst system can be adjusted to meet your specific needs. Diagnostic information, such antecedents and consequences, locations, times, etc. Topographical behavior data such as frequency, severity and duration.

The premier clinical trial management system, specifically designed to overcome the technical challenges of managing clinical trials. CTMS Master makes it easier for users to communicate, reduces manual work, and eliminates redundant data and tasks. This allows for more efficient trial conduct. A Site Visit Report tool that integrates with an automated workflow eliminates duplicate data entry. It also facilitates the creation and distribution of out-of-the box Site Visit Reports (SVR). Standard templates can be used for site and project documents, budgets, events, milestones and site visit reports. CTMS Master offers more than 100 metrics/statistics to help you track clinical study sites, countries, and projects. It also includes 80+ standard reports and ad-hoc reporting capabilities. CTMS Master allows you to create site-specific budgets using a default template, track accrued and future obligations, and define automatic or manual approval for each payment type.

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.

Collaboration and document control. myClin is an eTMF platform that allows for collaboration and collaboration. You can upload and share your study documents on myClin's secure central channels. You can access your documents quickly and receive critical updates and training faster. You have full control of your data. The "File it!" feature allows you to see who has read and understood your study materials. You can record evidence of study execution and review training actions such as views, filing or downloading at individual or team level. Inspection readiness. Always be ready for inspection. Our compliance score shows how compliant each study site or team member is with the appropriate study information. You will be guided to areas that are less compliant in your study. This helps you improve risk management. We will create a myClin channel so you can share myClin with the team in just a few hours. It's that simple.

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.

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.

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.

One platform to research, document, and collate your clinical data. The Nucleus platform simplifies research data. One platform to store all your study documentation, clinical data, submission data, and compliant media. Nucleus Documents allows you to manage and control your media and quality documentation. You can easily manage, control, and share company content. Our centralized regulatory document management solution makes it easy to manage and collect electronic trial master files. Nucleus Coding allows you to code dictionary terms against both WHODrug and MedDRA dictionaries. It can be used in our standalone application or integrated into your data capture software.

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.

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.

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.

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

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

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.

Preclinical information is found in many laboratories. It can be stored in multiple systems within the laboratory and with several external partners. Team members are unable to have clear and informed decisions without a unified solution because they lack transparency in core business data. Pristima, a fully integrated digital laboratory execution platform, features intelligent workflows, task automation, and data and information management throughout the entire preclinical process. Xybion's preclinical platform provides a central data repository as well as a standard archive platform. This platform can help you increase productivity and lower costs. With complete transparency across all platforms, gain visibility into the information that is there and take actions based on your current business needs. Effective data management can reduce the time it takes to submit final SENDs from end-of-study.

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.

Clario CTMS is a user-friendly, intuitive, end-to-end management system for clinical trials. It brings control, efficiency and quality to data flow and workflow. This results in cost savings in time and labor, as well as operational and operational expenses. This web-based CTMS allows you to view and manage your operational performance anywhere and anytime. Clario CTMS, a Microsoft Office-based workplace environment, transforms disjointed clinical trials into a cohesive and efficient work environment by using the most popular office productivity tools around the globe. Clario CTMS can seamlessly exchange information with SharePoint and other Microsoft products. This makes it a powerful, high-performance system. Integrating Office processes with clinical operations can reduce paperwork, significantly lower administrative overhead, and result in a low total cost of ownership.

Ofni Clinical is a clinical database management tool that creates and quickly implements secure, regulatory-compliant clinical trial databases. Ofni Clinical offers comprehensive search and report capabilities, strong data validation and edit-check options, flexible customization tools, and is easy to implement quickly and economically. The databases can be used to collect data from existing Case Report Forms as well as electronic data capture systems that are paperless. Most Ofni Clinical projects take less than a month from project initiation to validation. Contact us today to learn more about Ofni Clinical and how it can be used for clinical trials. It matches your existing Case Report Forms, reducing training and implementation expenses while adding electronic data capture & review capabilities. Features include extensive edit checks and data validation to detect and correct data entry errors and support data analysis.

A scalable, real-time, collaborative, out-of-the box solution for CROs, Life Science Consultants and Industry Stakeholders. Built in an Audit Ready Compliant Cloud environment (ARCC). All 21 CFR Part 11 requirements are met. GxP audit ready. Pre-configured Departmental. Communications with internal and external stakeholder. Secure data integration between remote teams. Collaboration in review and approval. Turn access on/off according to need (EX: auditors), reducing audit prep time from days to hours. Preconfigured to eTMF Reference models & EDM. Intelligent content management tools can improve workflows. Improve document management with real-time collaboration, automatic indexing and co-authoring. Pre-configured, validated system that manages documents and data electronically in accordance with eCTD mandates.

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.

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.

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.

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

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.

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.

Clindata Cloud is able to receive pre-clinical, clinical, and Risk Metric data from multiple sources/sites. It empowers clinical operations teams with submission-ready data sets and analytics, as well as risk-based monitoring alerts and risk-based monitoring alerts. Consolidate and harmonize study data from multiple sources into a comprehensive data model. Validate the data received for completeness, accuracy and consistency. To eliminate noise and create submission-ready data set in real-time, standardize data according to CDISC data standards. Based on standard data, generate submission-ready analytics in real time.

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.

Novatek's Clinical Assay Management software provides a consistent approach for the collection, management, and integrity of clinical research data. Novatek's Clinical Assay Management software tracks all sample data and manages them throughout the entire analytical process. It also ensures that there is a single verifiable version of all clinical and analytic data sets. Novatek's Clinical Assay Management Software helps organizations manage their studies based upon a specific product. This application will also give the structure required to ensure that all steps are completed in a timely fashion.

Ethical eAdjudication combines innovative endpoint adjudication technology with e-clinical software. Ethical eAdjudication is a cloud service that is intuitive and easy to use. It is designed for committee members, study leaders, QA staff, as well as committee members. Users can use Ethical eAdjudication to perform independent review and adjudication in a timely, quality-controlled, and effective manner.

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.

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

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.

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.

All the power and functionality of a powerful, integrated clinical data management system (CDMS), Clinical Trial Management System(CTMS) or Electronic Data Capture System(EDC). Our innovative, flexible, and compliant Clinical Trial Software System can provide all your study information. Your servers or ours. Clindex®, which can be installed on your server or on the Fortress Medical Cloud (SaaS – Software as a Service), is available. Cloud access is available worldwide and your data is stored in a SOC 3 certified data centre. We can build what you can dream of. Clindex®, provides all the tools necessary to create your own study database. The help documentation and quick start manuals will guide you through each step. Our Clindex services team can also create a study for your company.

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.

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.

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.

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.