Alternatives to ResearchManager

Labguru, a cloud-based Electronic Lab Notebook, LIMS and Informatics Platform that offers a complete solution to life science research and industry, is secure and reliable. It records and manages laboratory data, inventory, molecular biology tools, and chemistry tools. This allows labs to run more efficiently and automates lab operations. Labguru allows scientists to design experiments and workflows. They can also capture structured and unstructured information, manage projects, and share their results. You can create custom-designed experiment templates and integrate protocols, SOPs and other cutting-edge features to improve data quality, streamline workflows, and reduce costs. Labguru is available via the cloud on desktops as well as mobile devices. Labguru is part Holtzbrinck Publishing Group. It serves more than 100,000 scientists from universities, research institutes, startups, and large pharma companies around the world.

Bipsync combines your entire research process into one intuitive, powerful platform. The Bipsync Research Platform has been proven to increase productivity, improve collaboration, and simplify compliance. It was designed to assist professional investors in managing and accelerating their research.

Turnkey research management solutions can help you get funding, deliver results, manage everything in between, and do it faster and more efficiently with eRA Research Software. More corporations, universities, and research institutions worldwide have chosen the InfoEd Research Software Solution in order to save money, improve data integrity, manage administrative processes, accelerate compliance for electronic research administration, and make it more cost-effective than any other research compliance software. Our core belief is that industry knowledge and experience are the foundation for superior software development in research administration software. This has led to an unrivalled suite of research support technological apps, professional services software, and industry education programs by InfoEd Global, specifically designed to meet the needs of modern research institutions.

Dynamo brings the moving pieces that go into smart, successful alternative investment management into one integrated, configurable platform. All of our modules can work together on one technology stack to build one centralized, automated, and comprehensive platform for private equity and venture capital funds, real estate investment firms, infrastructure, hedge funds, endowments, pensions, foundations, prime brokers, fund of funds, family offices, and fund administrators. Dynamo does the heavy lifting and automates repetitive and manual processes with configurable dashboards, workflows, and reports. This way, your team can focus efforts on the human touch and insights that make your firm succeed. Dynamo’s long-tenured Client Services and Support team is committed to delivering excellence and ongoing wins as you embrace the platform for your unique business needs.

Our AI-powered research platform helps you fight information overload. Natural language processing and automation will make your research more efficient. This will allow you to spend less time searching and more time analysing. Your team can seamlessly collaborate with one another using our integrated research notebook. Find information that others have missed and generate alpha from linguistic or alternative data. Combat information overload. We process millions upon millions of data points to surface the information you need to stay ahead in the markets.

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.

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

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.

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.

EDGE, a cloud-based Clinical Trials Management System, has been successfully integrated into the UK's clinical research infrastructure and the devolved countries. Currently, EDGE is used in 80% of England's NHS regions, Scotland, and Northern Ireland. EDGE is the leading research management system in the UK. EDGE was launched in 2000 and adopted by the National Cancer Research Network. It has seen tremendous growth and has a growing number international subscribers from countries which include Canada, Belgium, New Zealand, South Africa and India.

The research business is all about getting your research read, valued and paid for. The Connect solutions are a modular, flexible set of services that world flow has designed to address these issues. It is important that your Research is easily accessible and discoverable by clients. We solve this problem by combining a Research Portal with Native Apps, Emails with tracking and links, push to Aggregators and consolidated readership, all backed up by flexible Authoring. Create a variety research, market color and commentary, as well as news, using template-driven authoring tools. Manage your balance sheets, macro-numbers, and company fundamentals centrally by sector, country or individual coverage. Email distribution tools allow you to keep your clients informed about the latest product releases and news.

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.

iOMS For Research Teams(c), was developed in collaboration by The Royal Wolverhampton Hospitals NHS Trust. It contains a cohesive integrated set of modules that helps all stakeholders effectively manage research management areas. All stakeholders can access a single platform that provides real-time views and engages them in research. Decision making is made easier by the inclusion of drill-down and detailed reports.

Pillar science offers software tools that are specifically designed to help you manage your research. We help you and your research team to focus on your research. Pillar Science is simple to set up. It connects your tools: you can enter data in spreadsheets and type protocols in word processor. You can also communicate in real-time. It covers all your research needs, so you don't have to duplicate any information. We use established security procedures to encrypt your data and store it securely wherever you need it. All your data are automatically backed-up. Pillar Science fine-grained authorization allows you to control who has access. Pillar Science will help your team follow standard methods and SOPs in your research. GxP research can be done using electronic signatures and FDA 21 CFR Part 11 compliance. To ensure regulatory compliance, you must decide where to store your data.

The illumin Knowledge & Research Management System records, quantifies, and precisely answers questions and answers given to clients and staff. It is the ideal tool for knowledge and research management. It is easy to customize and will fit every library's unique reference workflows. The knowledge base is automatically created and can be searched for relevant information. This allows for easy sharing. You can manage the large amount of knowledge in your organization easily and have it available anywhere and anytime. Softlink's Liberty, illumin and other tools make information easily accessible to your users. Your library can lead the way into the future. illumin is a great tool for knowledge management and research management. It records, quantifies, precis's questions and answers and provides them with the information they need.

OpenText™, a leading provider of information management solutions for life sciences organizations, helps them to harness insights from data and content to improve their decision-making and accelerate product development. Integrate, manage and securely exchange data between people, systems, and things. Use information assets to drive innovation and commercialization. Cloud-native software can run anywhere, giving you freedom of choice. OpenText for life sciences accelerates discovery by delivering actionable insights that can be used to drive innovation in pipelines. Intelligent capture allows you to capture and manage research papers in electronic lab notebooks. Text mining can help you gain insights. Unstructured text in clinical trial reports, study protocol, clinical safety and efficiency findings, can be used to extract knowledge. Learn how to intelligently analyze and classify clinical trial documents and extract them to reduce the risk for costly stops and starts.

CalibreRMS, a complete Research Management System, has an intuitive interface that allows you to record, share, and collaborate on data in a mobile-friendly, customizable, and user-friendly format. Calibre RMS is more than a note management tool. It seamlessly integrates your qualitative research with your modeling, analytics and modeling. It can be customized to your investment strategy and allows for immediate collaboration between teams from any location and on any device. Calibre RMS allows you to integrate it with other modeling tools and analytics tools without being locked in a proprietary system. It also includes audit trails to simplify compliance.

NoodleTools is an online platform for managing research that encourages authentic research and critical thinking. Students learn how to organize themselves as they analyze information, create accurate citations and archive source material. They also take notes, outline topics and prepare for writing. Students can access three levels of support that are tailored to their abilities and grades. The classroom environment allows teachers and librarians to give feedback, monitor individual contributions to group works, and view statistics on source use. We support students to engage in deep research and create original work, unlike an auto-cite or auto-evaluate product. NoodleTools was also created with student privacy in mind. Recognize and assess credible sources. Expert assistance is available to help you generate accurate MLA, APA and Chicago references. Create connections, make original ideas, and present arguments.

Cortellis™, a suite of life science intelligence software solutions, reveals hidden insights in data. This allows you to make better informed decisions throughout the R&D process. We have taken out the tedious work of finding, integrating and analysing data so that you can concentrate on the crucial decisions required to bring your products to market quicker. Cortellis provides unique data analysis that is rich in domain knowledge, industry insight, and therapeutic expertise. This allows you to unlock hidden insights that will allow you to make data-driven decisions that drive innovation. With the most comprehensive and deepest intelligence, you can get precise and actionable answers to specific questions throughout the R&D process. Cortellis is an indispensable part your daily work flow.

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.

Worktribe, a cloud-based platform for software development, transforms higher education administration by facilitating better collaboration, greater efficiency and greater transparency. End-to-end, seamless research management from conception to publication and beyond. For higher education teams, we offer intuitive, secure, cloud-based, curriculum management. We have worked with UK higher education institutions to create the best platform for curriculum management and research. It is intuitive, cloud-based, and built for efficiency, transparency, and collaboration. Continuously evolving to meet the challenges in HE administration. Trusted by 38 top UK universities and now available on Google Cloud. Worktribe is being used by more people every year to create teams and not regimes. Worktribe is the best cloud-based software platform to manage curriculum and research in higher education.

Qiqqa secures all PDFs and makes them searchable on all devices. You don't have to hunt for the missing paper again with automatic identification, tagging, and categorization. You can capture all your annotations, comments, highlights, and tags while you read PDFs in Qiqqa. You can then use powerful annotation reports to quickly review what you've read so that you don't forget the important details. Qiqqa helps you navigate through the literature and understand your research niche. It then highlights the most relevant and influential papers in the niche. Qiqqa allows you to find the next paper by following keywords, authors, and citations. Qiqqa's themes, annotation reports and search function will show you everything you need to cite in every section of your paper.

The amount of information required for investment decisions and due diligence is overwhelming to modern investment managers. Research management is a complex process that involves many sources. It can be difficult to identify and find the most important information. Tamale, the investment research management software we offer, allows investment teams to spend more time on ideas and less time searching for data. Tamale RMS allows investment managers to quickly search for and find important documents and records. Tamale's mobile experience is fast and flexible, allowing them to make better informed decisions faster. You can achieve a repeatable, disciplined due diligence and decision making process. Tamale RMS was designed by and for investment professionals.

Zotero is the only software to automatically detect research on the internet. Do you need an article from JSTOR? Or a preprint from ArXiv.org. Need a news story from The New York Times? Or a book from a library. Zotero covers everything. Zotero makes it easy to organize your research in any way you like. You can organize items into collections and tag them using keywords. You can also create saved searches that fill automatically with relevant materials as your work progresses. Zotero can optionally sync your data across devices. This allows you to keep your notes, files and bibliographic records up-to-date. You can access your research from any internet browser if you choose to sync. Zotero allows you to co-write a paper, distribute course materials, and build a collaborative bibliography. You can share your Zotero library with as many people as you wish, and it is completely free.

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.

Verity is the only platform that integrates investment research & data into a modern research workflow. One platform that combines best-in-class idea generation, workflow & productivity tools allows you to power differentiated research at the speed required for modern investing. Verity analysts provide unique insights and data to help you succeed. Verity integrates better that any other solution. It should be your process or the highway when it comes to your process. Verity provides investment professionals with clear, accurate, and structured information. You will receive your reports via email or custom feeds. The Verity team of analysts produces 100s of reports each year that customers value as an addition to their in-house analysts.

ANALEC believes that technology and software can help full-service brokers-dealers combat the structural decline they face and reset their business models so that they remain sustainable. Our offerings help brokers to increase productivity and cost-competitiveness, as well as improve revenue generation prospects. Over the last decade, institutional stockbroking has faced significant headwinds. Intense competition and regulatory scrutiny, as well as declining commission pools, have all contributed to the economics of this business. We have also seen a growing difference between clients' expectations of value-add versus broker compensation expectations. Investment research as a packaged service has not been commercially attractive.

Science 37 is a company that specializes in clinical research. Its Metasite model eliminates the physical distance as a barrier to participation, allowing patients to participate anywhere. This approach allows access to more than 90% of patients that are not able to participate in site-based research. It offers the recruiting power of twenty sites in one, and provides the flexibility needed by patients to participate from anywhere. The Metasite is powered a proprietary platform which drives uniform study orchestration. It guides the workflow of study staff and patients, and captures study data without requiring manual reentry. This centralization of platforms, people, and processes ensures protocol compliance. It also ensures high-quality data. Science 37's medical teams, telemedicine researchers, and mobile nurses are experienced in conducting remote trials in various therapeutic areas.

Flatiron Health's Evidence Solutions provide a flexible way to generate both prospective and retroactive real-world evidence. This allows life sciences companies to accomplish their oncology research objectives more efficiently. Flatiron Horizon is the core of these solutions. It integrates a vast repository with over 5 million deidentified patient records, 1.5 billion data points and advanced curation methods. This platform supports different stages of the biopharmaceutical lifecycle including discovery, clinical studies, regulatory submissions and post-marketing obligations. Flatiron's services include real-world data configurations tailored for specific oncology requirements, prospective evidence generation via low-interventional study, protocol optimization, identification of patients, and seamless EHR to EDC data transfer via Flatiron Clinical Pipe.

Outwit your competition. All-in-one Amazon seller software suite. You can easily manage, research, and automate all aspects of your Amazon business. There are no restrictions on the number of products you can manage. Perform vital tasks and access essential data across your vast catalog. Multiple seller accounts. Multiple Amazon seller accounts can be managed under one roof. You can easily compare your vital statistics across all accounts, individually or together. Delegating is essential for any large business. So that your employees can do their jobs, create sub-accounts with restricted permissions. Simple Transition. Easy transition from your current platform or Elite Seller without losing any data thanks to the 2 year backlog download. Customizable Dashboard. You can customize your dashboards to suit your needs. You can add widgets and tabs to track all your business metrics. All of the widgets and tabs can be adjusted to meet your specific needs.

Fibi is a cradle to grave eRA solution designed to meet the needs of research and higher-education institutions of all sizes. Fibi is an electronic research administration suite that normalizes and simplifies complex administrative procedures in managing funded research. Fibi allows seamless integration of extensions as well as external systems. Middleware of enterprise-class, built for rapid development. Independent Modules can easily be enabled within the system. Native app to connect and serve your key users with research administration. Fibi includes a variety of pre-packaged research reports that are tailored to the needs of research institutes.

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.

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 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.

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.

VACAVA Healthcare Solutions reduces the complexity and costs of regulatory document management for clinical trials. Documents can be lost or delayed if they go through a manual workflow. VACAVA solutions streamline regulatory processes by storing forms, profiles, and documents in one easy-to-access online place. With electronic approvals, documents can seamlessly move through your workflow (21 CFR Part 11 compliant). Easy-to-read dashboards enable efficient management. VACAVA's Regulatory Document Management System was developed in collaboration with a major clinical research base to simplify operations, and dramatically increase efficiency. VACAVA's Regulatory Document Management System can be tailored to your specific needs. It is surprisingly affordable. VACAVA's solutions can be customized to meet your unique needs. They are flexible and scalable and delivered via cloud so that you don't have to worry about security and backups.

Dasseti offers software solutions for the due diligence and monitoring process of asset and funds managers. Dasseti provides a powerful and flexible set of features that automates and digitizes assessment of funds. These include: digitized due-diligence questionnaires engine; automatic flexible responses flagging, scoring and management engine; research management and reviews management; CRM, collaboration and workflows; external managers portals and analytics ..... Our goal is to assist investors and investment consultants in increasing efficiency of their due diligence and monitoring process through digitization. Dasseti solutions help investment consultants, sovereign funds, pension plans and foundations, endowments and family offices, wealth management firms, funds of funds, insurers, banks, and funds of funds select or monitor managers across asset classes.

Our Smart Protocol system is designed to automate and add intelligence to clinical trials design with AI. Smart Protocol is revolutionizing how research teams design clinical trials. Humans can no longer physically digest all the information necessary to make a decision in today's digital age. A majority of companies have valuable data that isn't being used. Documents are stored in repositories without any line-of-sight. Companies in life science are making costly and difficult decisions based on incomplete information. We want to transform companies like yours' from a document-driven environment to one that is data-driven. We aim to reimagine how clinical trials are planned and researched by removing barriers between data and end users. We do this by mining huge amounts of trial-related documents both from customers and the public domain.

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.

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.

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.

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.

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.

Complion's platform was designed for clinical researchers. Our solution ensures compliance at the highest level with the lowest effort and the most efficiency. This allows you to concentrate on what really matters: improving and advancing patient outcomes. Our eReg solution is available to all clinical trial stakeholders, whether you are a Sponsor, Research Site or CRO. Reduce costs, avoid redundancy and increase staff productivity. You can easily archive, view and get signatures from any device. An audit trail is built into the system to ensure accuracy and eliminate patient safety risks and study conduct. Our clients include hospitals, cancer centers, and medical centers as well as multi-specialty clinics and dedicated research sites.

ClinicalWave.ai, built on AWS' cloud platform, is an integrated AI platform designed for life sciences companies. It uses cutting-edge NLP to extract valuable insights and automates the redaction and extraction sensitive data from clinical documents. It is made up of: 1. ClinRedact AI - Our Redaction Product that automatically identifies and removes sensitive information from clinical documents. This product saves time and ensures data integrity. 2. ClinExtract AI - The AI Data Extraction Product that uses NLP and Machine Learning to extract relevant data from clinical documents. This product provides valuable insights and streamlines workflows. 3. ClinDICOM AI - Experience the power and features of our DICOM data extraction product. It offers targeted redaction, customizable redaction rules, intelligent context analysis, audit trail compliance and a user friendly interface.

Cytobank, a cloud-based platform that allows for analysis, storage, sharing, and sharing of mass cytometry data, is available. Cytobank can be accessed via the internet using a web browser and an existing account. Cytobank does not require any additional software or hardware to be installed, updated, or maintained. Both license types have the same functionality. This license is ideal for large research groups, pharma, biotech R&D teams, clinical research organizations, and other clinical research organizations. Private Cloud, Access is controlled by an administrator role. Larger compute caps for functionality such as viSNE

Truveta, a platform for health data and analytics, is dedicated to saving lives through data. Truveta aggregates de-identified electronic records from more than 30 health systems to provide researchers with comprehensive patient data including clinical notes and genomics. This vast dataset includes more than 120,000,000 patients and provides a representative view on patient care in the United States. Truveta Studio is the platform's integrated analytical solution. It allows researchers to analyze specific populations using powerful tools such as notebooks and dashboards. All of this takes place in a secure HIPAA-compliant setting. Platform data is updated every day, ensuring timely insight into patient care and outcomes. Truveta is committed to data quality, as evidenced by its use of Truveta Language Model. This AI model, which includes large-language and multi-modal AI, transforms EHR data to clean, accurate data points that can be used for medical research.

ConcertAI is the leading provider of AI solutions for the healthcare industry. They specialize in oncology. Their mission is to improve patient outcomes by accelerating insights using real-world data and AI technologies. ConcertAI provides a range of products and services that are designed to improve clinical research and patient care. Their Real-World Data Products offer comprehensive, fit-for-purpose data sets that support a wide range of research needs within the enterprise. The digital trial solution streamlines the clinical trial process, while the Clinical Trial Optimization platform (CTO) uses large-scale AI for trial design and execution. ConcertAI, in collaboration with NeoGenomics has developed CTO - H, a SaaS offering advanced research analytics, and operational optimization, for hematological malignancies.

The new eTMFConnect is now available. Simplicity without compromise. We have re-engineered eTMF Connect to make it more scalable, faster, and more efficient for today's clinical trial environment. Improved Data Visualizations and Reporting Views. Montrium now provides a variety of new data visualizations and reporting tools integrated into eTMFConnect, allowing for more powerful business intelligence applications. Project teams and clinical operations managers will have greater visibility into TMF quality, timeliness, and completeness with better functionality. These improvements will help you elevate your TMF strategy across clinical programmes. Every clinical trial is different. The subtle nuances and regional differences can add layers of complexity that can keep even the most skilled TMF professional awake at night. Your eTMF platform must be flexible enough to handle these nuances and differences.

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.