Alternatives to EDGE

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.

OpenClinica is a leading provider of clinical data management software solutions. OpenClinica provides powerful tools to ensure that clinical trials are compliant and efficient. OpenClinica Enterprise, OpenClinica Participate and OpenClinica Randomize are the core products.

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

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.

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.

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.

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.

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.

Accelerating the development and delivery of life-saving medicines, and enabling cancer patients to have access to the best quality of cancer research and care. Our software revolutionizes patient access to innovative drugs & clinical trials. FICS is a software that allows the collection of regulatory standards data during patient care. FICS combines traditionally separate and noncommunicating applications to create a novel end-to-end platform. This allows clinical trials to be performed faster, easier and with greater quality.

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.

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.

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.

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.

This company offers a variety of clinical trials management solutions suites for various CROs, Pharmaceutical and Biotech industries. BizNET-CTM is a multi-functional platform that allows a CRO (Contract Research Organization), to plan, manage, design, execute, monitor and analyze trial-related activities and data in compliance with regulatory requirements and protocol obligations. A complete solution suite that addresses all aspects of clinical research projects, from Project Management to feasibility assessment to patient or volunteer enrollment using iris recognition technology to capture clinical trial data and multi-level review to data archiving. BizNET-CTM Suite is designed to manage all documents, tasks and processes, audits, relationships, audits, training, and other information that are required throughout the life of a clinical study.

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.

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.

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.

The industry's best eSource, CTMS and eRegulatory software. CRIO's electronic source is the best in its class and allows you to capture source data instantly and in real time. You can eliminate up to 90% of paper and improve data quality by as much as 80%. CRIO's intuitive clinical trial management system will help you take control of your operations. You can schedule patients, track financials, streamline recruitment, and much more. Electronic regulatory binders are now ready for the 21st Century. This includes the first ever electronic delegation log, all 21 CFR Part 11 compliant. Clinical trial sponsors can now remotely monitor your sites' source data, and regulatory documents via an online portal. Join our network of 500+ clinical research sites from around the world. Our mission is to help your business grow. We help you streamline your site's operations so that your studies don’t stop because you aren’t in the clinic.

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

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

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Medilake is your premier solution for comprehensive clinical and non-clinical trial data management We are pleased to introduce Medilake, a versatile and innovative platform that excels at the seamless management of clinical trial and nonclinical trial data. Medilake is the best choice to simplify, optimize, and enhance data management processes in an era when data is the lifeblood for healthcare and research. Why choose Medilake to manage clinical and non-clinical trial data? Unified Data Hub - Streamlined collaboration - Data Integrity & Security Advanced Analytics - And Customization and Scalability

Cloudbyz CTMS is a cloud-based trial management platform natively built on Salesforce Cloud. It is aimed at sponsors, clinical research organizations (CRO), and clinical sites for managing end-to-end clinical trial operations. Designed for clinical research, it expedites implementation and drives user adoption. Cloudbyz CTMS comes with an intuitive, straightforward design that allows for quick deployment. Boasting a rich set of features, Cloudbyz CTMS makes it easy for users to manage all aspects of clinical trials, including sites, enrolment, documents, events, milestones, site visit reports, finances, inventory, etc. The solution benefits are listed below- 1. Secure, reliable & scalable 2. Faster time to value 3. Monitor study progress & risks from planning to close-out 4. Seamless collaboration among sponsors, CROs & sites 5. Improved clinical team efficiency

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.

Flexible eCRF platform that can be used for non-commercial clinical trials. It can be configured to any clinical trial protocol. Our eCRF solution was developed from the many years of experience gained by researchers and medical teams who collaborated on research projects. The system is easy to use, user-friendly, and very flexible. The prepared solution meets all quality standards. We have full control over the code and can continue to develop it and adapt it to meet the changing needs of regulators and clinical trials market.

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.

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.

Formerly eClinicalOS IBM Clinical Development is a unified cloud-based data management platform. It offers a smarter way of collecting and managing clinical data. IBM Clinical Development is a SaaS solution that allows users to access all study data and platform functions via an intuitive and simple web interface.

ePharmaSolutions is building something new. We are not a high tech company. We are an idea-driven company whose thinking is deeply rooted in technology but not limited by it. We provide solutions to improve the management, activation, and training of clinical trial sites. We offer technology-enabled solutions that "un-complicate" clinical trial management. ePharmaSolutions is a leader in e-clinical solutions. Our solutions improve the selection, training, activation, and management of clinical trial sites. We bring new thinking to old problems and provide technology-enabled solutions to enable sponsors, contract research agencies, and investigator sites to "uncomplicate" clinical trial management.

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.