Alternatives to i-OMS

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.

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.

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

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.

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.

All researchers from different industries can use the same environment! ResearchManager is a platform that allows researchers to access all functions and information from one place. They can also share it with others. This platform is for researchers who are ready for the future. Future where patient and data access and sharing are central. We provide support for everyone involved in research in the life sciences sector. This is done through an online platform that includes the eClinical tools EDC and CTMS & ERMS. This allows researchers to share data and facilitates research at a higher level. We are also experts in the fields of data validation, enrichment, and collection.

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.

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.

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.

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.

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.

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.

OmniStar: the most powerful Grants, Ethics & Research management solution. Designed in consultation with research professionals and funders over 20 years, OmniStar is a comprehensive and flexible suite of products purpose-built to streamline the work of researchers, administrators and grant managers. Make confident grants, research and administration decisions. Why makes us different? • Intuitive User Experience: OmniStar boasts a user-friendly interface designed with simplicity and ease of use in mind. • Dedicated Support: Our team of experts provides exceptional customer support. From onboarding and training to ongoing assistance, we are here to ensure you extract maximum value from OmniStar. • Flexibility and Configurability: OmniStar is highly customizable, allowing you to tailor workflows, forms, email and document templates and reporting to align with your specific requirements. • Scalability and Adaptability: Whether you manage a small or large number of grants and research projects, OmniStar scales with you. • Continuous Innovation: OmniStar is committed to continuous innovation. We consistently update and improve our platform based on user feedback, industry trends, and emerging best practices.

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 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.

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.

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.

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 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.

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.

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.

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.

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.

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.

Clinical Conductor CTMS (Clinical Trial Management System) is a cutting-edge system for managing clinical trials. It's suitable for hospitals, research sites and asset management companies. Site networks, health systems, contract research organizations (CROs), and other healthcare facilities. This cloud-based solution makes clinical trials more efficient and helps research organizations make better business decisions. The key features include electronic data capture and enrollment management, document management, recruitment management, and many more.

We offer data to support your workflow, analytics that will help you outperform, as well as insights to give perspective. FactSet assists over 6,000 financial service firms with their most pressing problems, including optimizing technology costs, creating integrated workflows, mitigating risks, and creating efficient data governance within an organization. Our comprehensive data feeds, web and mobile analytics, and white-glove customer service transform the way investment professionals discover, decide, then act on opportunities.

To make health breakthroughs more rapid, people must be involved in research. We have created a platform that connects individuals, communities, researchers, and others through trust, transparency, shared value, and shared benefit. Every person has unique information that could lead to the next medical breakthrough. Sharing your health data can help uncover new insights. Communities bring people together to quickly find answers. We manage your data and health experiences so you can start right away. We bring together individuals and communities to share their health data in order to answer the most pressing questions of life. People can unite with a common vision of fairness and responsibility, and it can change the face of established systems and institutions. A team of passionate technology and genomics leaders created it.

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.

Teckro clinical trial software connects all stakeholders to crucial information. Every time. Everywhere. Every day, we find answers from our smartphones. The same applies to clinical trials. Research staff and CRAs always have access to the most current study information. Research staff can access the most important details via their mobile devices by simply tapping a button. Site staff and monitors can be notified in real time if any updates or amendments are required. Teckro, a cloud-based clinical trial software that runs quickly and requires no installation, is quick and easy to set up. It's easy, intuitive, and simple. Teckro is secure hosted and in compliance with major industry regulations, such as FDA 21 CFR Part 11. You don't need to worry about version management as long as you have the approved version of the study documents.

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.

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

Longboat, a cloud-based clinical support solution, provides users with an integrated Guided Compliance toolet to help them at all times. Longboat gives clinical trial staff the resources they need to focus on patients. Longboat allows patients access to essential study information and reminders for their visits. Longboat makes it easy to manage the controlled rollout and revision of the clinical trial protocol.

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.

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.

MEDAS HIMS, a web-based ERP software for small- to large-level hospitals, provides enhanced patient care, real-time data sharing, revenue generation, and operational efficiency. This browser-based system can be used with a variety of devices to allow for accurate and easy data capture. The system's well-defined workflow allows organizations to manage OP/IP functions efficiently and effectively, while ensuring high patient satisfaction. The integrated, advanced EMR module captures maximum information and allows for easy, safe and secure access. Multi-tenant architecture allows for the management of multiple sites/locations.

IQVIA is trusted by thousands of organizations worldwide to accelerate drug development, improve product quality and safety and commercial effectiveness, get the right treatments for patients, improve healthcare delivery and access, and ultimately drive better outcomes. Connect data, technology and analytics to optimize clinical development. The result? The result? Faster decision making and lower risk, so you can deliver life-changing treatments faster. IQVIA offers specialized capabilities to customers in the healthcare industry, thanks to its foundation in data, advanced analytics and expert insights. Watch the latest from IQVIA data scientists and doctors, as well as other subject matter experts, on the topics that are important to you. You can find everything you need, from industry trends to how our capabilities are being applied to help, here.

Ready by ArcheMedX for Pharma and Biotech Trusts to better equip their trial team, improve decision-making, and reduce study delays By understanding which sites and teams are best equipped to conduct the study, you can avoid the most common causes of study delays. Reduce the time and cost of resolving problems, especially early in a trial. You can be confident that the sites you choose truly understand your patient eligibility requirements. You'll feel more confident that they will be better equipped to help you enroll eligible patients faster, meet enrollment targets, and avoid screen failures. You can be confident that the trial team is fully conversant with the protocol, down to the individual and study objectives. You can predict where there are risks so that you can avoid them and have fewer deviations overall.

We create solutions that connect and empower clinical trial ecosystems. The Enrollment Performance Monitoring platform that sponsors love and sites rely on. It is used by over 2,000 research sites in 26 countries, and half of the top-20 global biopharma firms. Sites are able to move patients forward by spending less time on redundant and manual tasks. Sites do less double work. Sites and sponsors will have fewer logs, phone calls, emails, and emails. With real-time access and real-time data, sponsors can optimize enrollment. It is simple and easy to use, with over 1,800 sites in 26 countries using it for patient recruitment. To run more predictable and faster clinical trials, access powerful enrollment and recruitment insights. You can stop wasting time and get back to what matters most: helping patients. You can manage recruitment across all sponsors, trials, and CROs. Once you enter information, it will go where you need.

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.

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.

Research and clinical trials were traditionally conducted outside of local hospitals and doctors' offices. Patients didn't know that research could improve their health or their outcome, and doctors weren't always informed. Elligo allows for a wider participation in clinical research. With access to more than 150 million patients and their data (and more than 150 million others), physicians can offer research as an option to patients who otherwise wouldn’t have access. Traditional methods of recruiting are limited by geographical limitations, such as the proximity of patients to research sites. Patients prefer to work with their trusted healthcare provider.

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.

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.

We offer a level of collaboration that is not possible in traditional CRO environments. Our goal is to help you succeed in your clinical development program. Clinipace is a global, full service contract research organization (CRO) that focuses on clinical research. Clinipace offers a level of collaboration that is not possible in traditional CRO environments. We place a strong emphasis on personalized services, regulatory expertise, therapeutic leadership, and customized solutions. Our mission is to improve clinical research in major therapeutic areas such as oncology, rare diseases, gastroenterology and nephrology. Clinipace aims to make a difference in drug development and health care. We combine the most advanced technology with a CHALLENGE ACCEPTED approach.

Phoenix CTMS is a web application that combines the capabilities of database software used for clinical research in one modular system. The Phoenix CTMS is now publicly available (LGPL 2.0) after years of collaboration with trial sites at Medical University of Graz. This feature set is unrivalled and designed to meet all regulatory and operational requirements of the clinical front end of academic research at CROs (Contract Research Organisations), hospitals and clinics conducting clinical studies at any phase. A CDMS that supports unlimited Javascript form scripting (server-side and browserside) is what you need. You will need to deal with large electronic case report forms (eCRFs) Want to explore an open-source alternative to eCRFs. To create complex queries in ad-hoc databases to find matching candidates using set operations, You will need to conduct multiple trials simultaneously and organize staff and resources at each site. You will need software to implement different processes for ICH GCP.

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.

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.

Studypages is an integrated clinical trial management system designed to streamline clinical operations and unify participant experiences. It provides a set of tools to facilitate participant engagement, site administration, sponsor oversight, communications, collaboration, and workflow automatization. Studypages integrates these functionalities to create a single platform that increases the efficiency and effectiveness in clinical research. This accelerates the development of new medical innovations.

We help PIs overcome common problems and limitations in setting up and selecting databases. QuesGen can also be hired by researchers to provide advice on data management best practices, and additional services to help them get their studies up and running faster. Expert partner for many academic institutions and researchers. Our flexible data platform allows for data curation and management of large data sets. Ability to quickly set up and scale research projects. QuesGen provides a complete data model, an assessment library, and curation expertise. QuesGen makes it easy to get up and running quickly and ensures compliant data so you can concentrate on the analysis. You can support multiple clinical research projects at your institution with HIPAA- and FDA 21 CFR Part 11 compliant solutions. These solutions can be integrated with your EMR, FITBIR (Federal Interagency TBI Repository), and other EMRs.

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.