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 unifies your complete research workflow into a single, cohesive, and user-friendly platform. Demonstrated to improve efficiency, foster teamwork, and streamline compliance, the Bipsync Research Management Platform is meticulously crafted to assist professional investors in effectively overseeing and expediting their research endeavors, ensuring they stay ahead in a competitive market.

Gain access to top-tier information and insights regarding hospitals, medical professionals, and various healthcare providers, with daily updates ensuring accuracy. Our mission is to assist businesses throughout the healthcare landscape in expanding their operations and forging innovative pathways to success in the market. There are numerous reasons we have maintained our status as a frontrunner in healthcare commercial intelligence for over a decade. Driven by cutting-edge data science and artificial intelligence, we provide comprehensive intelligence tailored to all your business requirements. Healthcare commercial intelligence effectively clarifies the intricate network of data related to delivery systems, healthcare providers, insurers, patients, government entities, and more, allowing you to pinpoint the most suitable individuals, opportunities, and organizations for your offerings. Navigating the healthcare market with a new product can be challenging, as vital insights are frequently hidden within various fragmented data systems, complicating the quest for cohesive understanding. This is where healthcare commercial intelligence (HCI) steps in, representing a groundbreaking category of software that simplifies the complex data landscape surrounding healthcare delivery. By leveraging HCI, businesses can not only streamline their access to vital information but also enhance their strategic decision-making processes.

H1 Universe is an innovative platform that leverages artificial intelligence to enhance the management of healthcare data, offering users access to the most extensive global database of healthcare providers (HCPs). By merging information from various sources, such as public, private, and proprietary databases, H1 Universe provides valuable insights that are crucial for clinical trials, medical affairs, and commercialization efforts. This powerful tool enables healthcare teams to pinpoint essential stakeholders, refine clinical research processes, and make informed decisions swiftly, ultimately boosting overall efficiency within the healthcare landscape. Furthermore, the platform not only aids in real-time decision-making but also fosters collaboration among healthcare professionals, paving the way for improved patient outcomes.

At Komodo Health, we integrate an extensive understanding of patient interactions with cutting-edge algorithms and years of clinical knowledge to create our Healthcare Map, which offers the most accurate representation of the U.S. healthcare landscape. This Healthcare Map serves as the backbone for our comprehensive suite of software solutions, designed to help you provide exceptional value to your customers, colleagues, and patients alike. Relying solely on traditional scholarly data for strategic planning is now outdated. Our Aperture platform has been meticulously crafted to deliver unparalleled insights into clinical leadership and influence, enabling improvements in care standards where they are needed most—whether that involves the most referenced author, a prominent social media influencer, or the physician with the highest patient volume. Moreover, conventional open/sampled prescription and patient-level data often overlook critical patterns that are essential for accurately identifying individuals with complex care needs or uncommon medical conditions. By addressing these gaps, we aim to enhance patient outcomes and streamline healthcare delivery.

Numerous organizations globally rely on IQVIA to accelerate the drug development process, guarantee the safety and quality of products, enhance commercial efficacy, deliver appropriate treatments to patients, and ultimately promote improved health outcomes by facilitating access to and delivery of healthcare. Transform your approach to clinical development by seamlessly integrating data, technology, and analytics to streamline your trials. The outcome? Quicker decision-making and minimized risks, enabling you to provide transformative therapies at a faster pace. With its expertise rooted in data, sophisticated analytics, and deep industry knowledge, IQVIA offers tailored capabilities to clients throughout the healthcare landscape. Stay informed by exploring the latest insights and updates from IQVIA's data scientists, healthcare professionals, researchers, and other industry experts on crucial topics that resonate with your interests. From emerging industry developments to practical applications of our capabilities, a wealth of information awaits you here. Engaging with this content also empowers you to stay ahead in a rapidly evolving healthcare environment.

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

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.

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.

Comprehensive research management solutions are tailored to assist you in securing funding, achieving outcomes, and overseeing all related processes more efficiently with eRA Research Software. Across the globe, a growing number of top-tier research institutions, universities, and corporate entities have opted for the InfoEd Research Software Solution to enhance cost efficiency, boost data integrity, streamline administrative workflows, and expedite compliance within electronic research administration, surpassing other options in research compliance software or eRA tools. We firmly believe that a deep understanding of the industry and its nuances forms the cornerstone of exceptional software development in the realm of research administration, leading to an unmatched collection of technological applications for research support, professional services software, and specialized educational programs by InfoEd Global, all crafted to meet the evolving needs of contemporary research environments. This commitment to excellence ensures that our clients are well-equipped to navigate the complexities of modern research endeavors.

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.

Combat the challenges of information overload with our advanced AI-driven research platform. By minimizing the time spent on searching, you can focus more on in-depth analysis, thanks to innovative natural language processing and automation that enhances your research efforts. Our collaborative research Notebook empowers your team to work together effortlessly, facilitating a more cohesive workflow. Harness the potential of linguistic and alternative data to extract valuable insights that others might overlook. Tackle information overload effectively as we analyze millions of data points and highlight the crucial information needed to maintain a competitive advantage in the markets. Sentieo is designed to help you discover alpha-generating insights from a variety of sources, including news, regulatory filings, market trends, historical data, documents, notes, financial fundamentals, projections, and more, all while keeping your team connected. With everything you need consolidated into a single workspace, Sentieo reveals insights that can significantly enhance your team's performance and decision-making. Ultimately, the platform ensures that your research capabilities are not only efficient but also strategically insightful.

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.

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

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.

The Medidata Clinical Cloud represents our innovative platform designed to revolutionize the clinical trial journey for patients, sponsors, CROs, and research institutions. As the sole comprehensive technology solution focused exclusively on clinical research, the Medidata Clinical Cloud addresses the entire research spectrum from inception to completion. Our platform enables organizations in the life sciences and medical device sectors to reduce development expenses, manage risks effectively, and expedite the introduction of treatments and devices to the marketplace. Whatever selection you make for your clinical trial initiatives, you will benefit from the capabilities of the Medidata Clinical Cloud. At Medidata, we are at the forefront of the digital evolution in clinical research. With the power of artificial intelligence, machine learning, and sophisticated analytics, our platform connects researchers, study coordinators, investigators, and patients, thereby hastening the research process. Additionally, it provides a regulatory-compliant, patient-friendly electronic informed consent solution for clinical trials, ensuring a smoother experience for all parties involved. This integration of advanced technology not only streamlines operations but also enhances the overall quality of clinical research.

Pillar Science offers specialized software solutions to streamline research management for you and your team, allowing you to concentrate on your studies. The platform is user-friendly and can be set up effortlessly, integrating various tools so you can input data into spreadsheets, write protocols in a word processor, and communicate in real time without hassle. It is designed to meet all your research requirements, eliminating the need for data duplication. With robust security measures in place, your information is encrypted and securely stored according to your preferences, while automated backups ensure you never lose vital data. The fine-grained authorization system allows you to control who has access to your information, enhancing confidentiality and security. Additionally, Pillar Science supports your team in adhering to standardized methods and SOPs essential for effective research. With features like electronic signatures and compliance with FDA 21 CFR part 11, you can confidently conduct GxP research. You also have the flexibility to choose your data storage location to maintain regulatory compliance, ensuring that your research meets all necessary standards. This comprehensive approach not only optimizes your research process but also enhances collaboration among team members.

Ensuring that your research reaches an audience, is acknowledged, and generates revenue is essential in the research industry. World Flow's Connect Solutions offers a modular and adaptable suite of services aimed at addressing these challenges. Making your research easily accessible and searchable for clients is crucial for success. By leveraging a combination of tools such as a research portal, mobile applications, email with tracking and links, distribution to aggregators, and integrated readership, all supported by adaptable authoring options—whether through Connect Compose or alternative industry solutions—you can effectively meet these needs. Additionally, you can produce a diverse array of research, market insights, commentary, and news using template-based authoring and composition tools. Moreover, you can manage your financial statements, macroeconomic data, and company metrics efficiently, categorized by sector, country, or specific coverage areas. Lastly, keep your clients informed about the latest updates, news, and product launches through effective email distribution strategies. This comprehensive approach ensures that your research not only reaches its intended audience but also maximizes its impact and value.

The illumin Knowledge & Research Management System is designed to efficiently collect, document, quantify, and summarize the inquiries and responses that staff and clients provide. Serving as an ideal solution for managing knowledge and research, it can be easily tailored to meet the specific needs of any library's reference processes. Its automatically generated knowledge base transforms into a thorough, searchable database of pertinent information that is readily shareable. Seamlessly handle the extensive flow of knowledge within your organization, ensuring that valuable information is accessible for discovery and delivery at any time and from any place. Both Softlink’s Liberty and illumin empower your library to provide information to users, positioning it at the forefront of future advancements. With illumin, you have a robust tool that not only collects and organizes data but also enhances the overall efficiency of knowledge management within your institution.

iOMS For Research Teams© was created in partnership with The Royal Wolverhampton Hospitals NHS Trust, featuring a cohesive and integrable suite of modules designed to assist all parties in efficiently overseeing various aspects of research management. This unified platform offers a real-time perspective that actively involves all stakeholders participating in research efforts. Additionally, it includes comprehensive and detailed reports that can be analyzed in depth, facilitating informed decision-making processes. By streamlining communication and management, it enhances collaboration among team members and stakeholders.

NoodleTools serves as a web-based research management system that fosters critical analysis and genuine research efforts. It aids students in maintaining organization while assessing data, crafting precise citations, archiving reference materials, taking notes, outlining subjects, and gearing up for writing tasks. With three tailored levels, the platform accommodates students of varying grades and skill sets, ensuring inclusivity. Additionally, the classroom setup enables librarians and educators to provide guidance, track individual contributions to collaborative efforts, and analyze statistics regarding source usage. Unlike automated citation and evaluation tools, NoodleTools encourages learners to engage thoroughly with their research and create original content. The platform is also designed with a strong emphasis on safeguarding student privacy online. Users can identify and assess pertinent, credible sources while generating accurate MLA, APA, and Chicago-style references, all with personalized assistance from experts. This holistic approach not only helps students forge connections and develop original ideas but also empowers them to articulate their arguments effectively, enhancing their overall research experience.

OpenText™ Information Management solutions empower organizations in the life sciences sector to harness data and content insights, enhancing their decision-making and speeding up product development. These tools enable seamless integration, management, and secure sharing of information among individuals, systems, and devices. By utilizing information assets effectively from research and development through to commercialization, organizations can benefit from adaptable cloud-native software that operates in any environment. OpenText for life sciences significantly accelerates the discovery process, facilitating the extraction of actionable insights that foster innovation in the pipeline. Users can convert research papers into electronic lab notebooks through intelligent capture, and uncover valuable insights using text mining techniques. Moreover, the platform allows for the extraction of knowledge hidden within unstructured text of clinical trial reports, study protocols, and findings related to clinical safety and efficiency. It also offers methods to intelligently analyze, categorize, and extract information from clinical trial documents, ultimately minimizing the risk of expensive delays and interruptions in the development process. By effectively utilizing these advanced capabilities, life sciences organizations can significantly enhance their operational efficiency and drive forward their research initiatives.

Qiqqa ensures the security of all your PDF documents while providing instant accessibility and search functionality on any device. With its automated processes for identifying, tagging, and categorizing your PDFs, you will no longer need to search endlessly for that elusive document. As you read your PDFs within Qiqqa, whether online at your desk or offline while traveling, you can easily capture all your tags, comments, highlights, and annotations. When it's time to revisit your readings, Qiqqa offers powerful annotation reports to help you remember crucial pieces of information. Additionally, the platform navigates your literature by gaining insight into your research area, showcasing both the most relevant and significant papers within that field. You can also discover your next reading material by exploring citations, authors, and keywords. Thanks to Qiqqa's themes and detailed annotation reports, you’ll have a comprehensive overview of everything to cite in each section of your manuscript, streamlining your research process. This not only enhances your organization but also boosts your productivity as you compile your work.

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.

Discover valuable insights within your data by utilizing the Cortellis™ suite of life science intelligence tools, enabling you to make more informed decisions throughout the entire R&D process. We have alleviated the burden of gathering, integrating, and analyzing data, allowing you to concentrate on the essential choices necessary for expediting your products' market entry. With a unique combination of extensive, high-quality data, fortified by profound domain knowledge, industry insight, and therapeutic expertise, Cortellis reveals crucial insights that facilitate data-driven decisions, ultimately speeding up innovation. Access tailored, actionable responses to your specific inquiries throughout the R&D lifecycle, drawing from the most comprehensive and in-depth intelligence sources available. By incorporating Cortellis into your daily routine, you can significantly enhance the pace of innovation and streamline your workflow. This makes Cortellis not just a tool, but a vital partner in your path to success.

Cytel stands out as a prominent global innovator in software for clinical trial design, biometrics, and advanced analytics, focusing on maximizing the efficiency of clinical trials while aiding pharmaceutical companies in harnessing the full scope of both clinical and real-world data. Established in 1987 by renowned statisticians Cyrus Mehta and Nitin Patel, Cytel has consistently been a leader in adaptive clinical trial technology and the field of biostatistics. Its software solutions, notably the East Horizon platform, facilitate accurate trial design and simulation, employing adaptive and Bayesian methodologies to enhance protocols and expedite the drug development process. The East Horizon platform serves as a comprehensive integration of Cytel's reliable software offerings, featuring R integration that significantly improves trial design functions. Furthermore, Cytel provides the Xact software suite, which is an all-encompassing toolkit designed for statistical analysis of small datasets, including those with sparse and missing data. By continuously innovating and expanding its product offerings, Cytel remains committed to providing cutting-edge solutions that meet the evolving needs of clinical research.

Zotero stands out as the sole software that effortlessly detects research materials available online. Whether you are in need of an article from JSTOR, a preprint from arXiv.org, a news piece from the New York Times, or a book from a library, Zotero is equipped to assist you at every turn. This tool allows for endless organization of your research, enabling you to arrange items into collections and categorize them with keywords. Additionally, you can create saved searches that fill automatically with pertinent resources as you progress in your work. Zotero offers optional data synchronization across various devices, ensuring that your notes, files, and bibliographic records are consistently updated. With synchronization enabled, you can conveniently access your research from any web browser, adding an extra layer of accessibility. Beyond individual use, Zotero facilitates collaborative efforts, allowing you to co-author papers with colleagues, share course materials with students, or compile a shared bibliography. You can effortlessly share a Zotero library with an unlimited number of collaborators, all at no charge, making it a perfect tool for group projects and academic endeavors. Such versatility makes Zotero an invaluable resource for researchers and students alike.

Worktribe is an innovative cloud software solution that revolutionizes the administration of higher education by enhancing collaboration, increasing efficiency, and fostering transparency. It offers a comprehensive research management system that guides users from initial concept to publication and beyond. Additionally, it provides a user-friendly and secure curriculum management tool tailored for higher education teams. Our collaboration with various UK institutions has led to the creation of an unparalleled platform designed specifically for effective research and curriculum oversight. With its powerful and intuitive features, Worktribe continuously adapts to address the evolving challenges faced by higher education administration. Trusted by 38 prominent universities in the UK, it is now accessible via G-cloud, broadening its reach. Each year, an increasing number of individuals are leveraging Worktribe's capabilities to foster teamwork rather than control. As the leading cloud software for managing research and curriculum in higher education, Worktribe stands out as an essential tool for academic institutions aiming to thrive in a dynamic educational landscape.

Harnessing actionable insights from the leading AI-driven clinical analytics platform allows your teams to effectively manage risk and enhance performance throughout studies, systems, sites, and vendor relationships. The cutting-edge technology from Saama is specifically crafted to optimize workflows, automate labor-intensive tasks, and foster improved collaboration among various clinical functions such as operations, medical review, data management, biostatistics, and pharmacovigilance. Both sponsors and CROs depend on Saama's capabilities for data aggregation and AI solutions, which facilitate superior decision-making, minimize delays, and drastically reduce costs and timelines associated with drug development. By leveraging Saama's tools, you can accelerate the pace of clinical trial innovation. When your clinical data is centralized and continuously updated, it simplifies the lives of your ClinOps and medical review teams considerably. Furthermore, Data Managers, often undervalued, can shift their focus from repetitive tasks to the critical data points that truly drive project success, ensuring that their expertise is fully utilized in the process. This transformation not only enhances efficiency but also contributes to the overall quality of clinical outcomes.

Contemporary investment managers often grapple with an overwhelming amount of information required for making informed investment choices and conducting thorough due diligence. The diverse origins of research management complicate the task of pinpointing what really matters. However, with Tamale, our investment research management software, investment teams can focus their efforts on collaborating over ideas rather than sifting through extensive data. Tamale RMS enables investment managers to swiftly access vital details about contacts, firms, funds, and relationships, thanks to its efficient search capabilities for crucial records and documents. By leveraging Tamale’s agile and user-friendly mobile experience, they can make quicker and more informed decisions. This ultimately leads to a structured and consistent approach to due diligence and decision-making processes. Designed specifically by and for investment professionals, Tamale RMS stands out as a dedicated research management solution tailored to meet the unique needs of the investment community. As such, it fosters a more productive environment where teams can thrive and drive better outcomes.

Outsmart Your Rivals. An all-encompassing software suite for Amazon sellers. Effortlessly research, manage, and automate every aspect of your Amazon business without restrictions on the number of products you can oversee. Carry out crucial tasks and dive into important data across your extensive catalog. Multiple Seller Accounts. Efficiently manage various Amazon seller accounts within a single platform, allowing you to analyze key metrics collectively or individually. A successful enterprise cannot thrive without delegation. Establish sub-accounts with restricted access so your team can effectively fulfill their responsibilities. Smooth Transition. Transitioning from your existing platform to Elite Seller is seamless, and your data remains intact thanks to a two-year backlog download feature. Customizable Dashboard. Adjust your dashboards to meet your specific needs, personalizing your control panel with different tabs and widgets that showcase all your business metrics. Everything is flexible, ensuring that the platform can be molded to suit your evolving requirements. With these robust features, your Amazon business can reach new heights of efficiency and success.

ANALEC is convinced that advancements in technology and software can significantly contribute to addressing the structural challenges that full-service broker-dealers face and assist them in re-evaluating their business models for long-term viability. Our solutions empower broker-dealers to enhance productivity and cost efficiency while also boosting their revenue potential. Over the past ten years, the realm of institutional stock-broking has encountered numerous obstacles. Factors such as fierce competition, increased regulatory oversight, shrinking commission pools, and the demand for unbundling commission payments to brokers have all put tremendous pressure on the industry's financial viability. Furthermore, there is an observable disparity between clients’ perceptions of value and the compensation expectations of brokers. The traditional model of providing investment research as a bundled service has struggled to maintain its commercial appeal in this evolving landscape. As a result, broker-dealers are compelled to innovate and adapt more than ever to thrive in a changing market.

Flatiron Health's Evidence Solutions provide a versatile method for generating real-world evidence, both prospective and retrospective, which aids life sciences companies in efficiently meeting their oncology research objectives. At the heart of these offerings is Flatiron Horizon, a comprehensive platform that combines a rich database of more than 5 million anonymized patient records and 1.5 billion data points, coupled with advanced curation techniques and disease-specific machine learning models. This innovative platform is designed to facilitate various phases of the biopharma lifecycle, including discovery, clinical study design, regulatory submissions, and post-marketing commitments. Furthermore, Flatiron's services deliver customized real-world data configurations that cater specifically to oncology, enabling prospective evidence generation through minimally invasive studies and optimizing protocols for better patient identification. Additionally, the platform ensures a streamlined transfer of data from electronic health records to electronic data capture systems with the functionality of Flatiron Clinical Pipe, enhancing overall research efficiency and effectiveness. Such capabilities position Flatiron Health as a leader in transforming oncology research through the power of real-world data.

Science 37 is a pioneering clinical research organization that focuses on decentralized clinical trials through its innovative Metasite model, which eliminates the need for physical proximity, allowing patients to engage in studies from virtually anywhere. This method significantly broadens accessibility, reaching over 90% of individuals who might be excluded from conventional site-based research, and harnesses the recruiting capabilities equivalent to 20 sites in one location, thereby offering patients the flexibility they desire. The Metasite operates on a proprietary platform that not only streamlines study orchestration but also facilitates the workflow for both patients and research staff, all while efficiently capturing study data without manual reentry. By centralizing personnel, processes, and technologies, this approach guarantees built-in protocol compliance, which leads to enhanced compliance rates and the collection of high-quality data. Science 37's dedicated in-house medical teams, telemedicine investigators, and mobile nursing professionals are well-versed in the conduct of remote trials spanning various therapeutic areas, thus ensuring comprehensive outreach. This commitment to innovative trial methodologies positions Science 37 at the forefront of transforming the landscape of clinical research.

Historically, managing clinical trials at investigator sites involved either the cumbersome task of maintaining numerous shared spreadsheets or investing in costly software that often did not fit the Australian context. MAISi represents a revolutionary shift in this landscape. Originating in 2001 as a data repository for clinical trials at a prominent hospital, MAISi has transformed into an advanced workflow application designed to streamline various functions within research units. Serving as a centralized database, MAISi efficiently organizes information related to studies and the corresponding business units that manage them. This structured approach enhances management decision-making capabilities. Individual staff members within each business unit can access specific data pertaining to their studies, patients, investigators, and study team members, while those with broader access rights, typically Financial Officers and System Administrators, can view comprehensive data across all units. Additionally, this streamlined access promotes collaboration and improves overall operational efficiency.

Fibi serves as a comprehensive eRA solution, tailored to meet the intricate demands of research administration and compliance management across institutions of all sizes within the research and higher education sectors. This all-encompassing electronic research administration suite streamlines and standardizes the complex processes associated with managing funded research initiatives. With Fibi, users benefit from smooth integration capabilities with various extensions and external systems. It features robust enterprise-class middleware that is specifically designed for quick development, allowing for flexibility and adaptability in its use. Additionally, independent modules can be activated within the system as needed, enhancing its functionality. A dedicated app is also available to connect key users to the research administration processes effectively. Furthermore, Fibi offers an extensive array of pre-packaged reports tailored to meet the specific needs of research institutions, ensuring that they have access to vital information when required. This holistic approach not only simplifies administrative tasks but also empowers institutions to focus more on their research endeavors.

AssisTek stands out as a frontrunner in cutting-edge clinical technology solutions tailored for clinical research, providing specialized software that optimizes and improves the process of gathering patient data. With a legacy of over 25 years, the company has successfully facilitated more than 800 clinical research trials spanning 46 therapeutic areas, which include upwards of 500 multinational Phase I–IV clinical trials. Their electronic Clinical Outcome Assessment (eCOA) solutions boast scalability, customization, and efficiency, backed by a reliable cloud-based technology platform. Among their extensive product offerings are the TEK eCOA Tablet, which accommodates any questionnaire utilized in clinical trials, TEK eDiary, enabling the collection of patient-reported outcomes from home, TEK Configurator for comprehensive project development in clinical trials, and TEK Study Portal, which consolidates eClinical tracking, training, and reporting into one convenient location. AssisTek's innovative systems and services have established them as the preferred partner for data collection and analytics, winning the trust of both patients and healthcare professionals alike. As they continue to evolve, AssisTek remains committed to enhancing the efficiency and accuracy of clinical research methodologies.

Modern Interactive Response Technology (IRT) systems are becoming more intricate. The significance of flexible and customizable IRT cannot be overstated, as this technology serves as the primary source for essential data, including recruitment metrics, clinical trial attrition rates, patient attendance, and more. It is vital to select a platform that is intuitive, optimized for mobile use, and all-encompassing—underpinned by high standards of quality, adaptability, and expertise. Embrace a partnership that offers profound therapeutic knowledge tailored to the contemporary risk-based eClinical landscape. By merging advanced technology with specialized knowledge and a dedication to exceptional service, we enhance clinical trials to achieve favorable patient results. Our extensive understanding of clinical processes and supply chain dynamics fosters innovation, granting clients greater control over their Randomization and Trial Supply Management (RTSM) protocols. Our cutting-edge tools elevate quality assurance, improve site productivity, and enhance patient adherence significantly. Furthermore, our IRT platform is adaptable enough to cater to a wide array of studies, with the capability for full validation and deployment in just 30 days, ensuring efficiency in clinical trial operations. This swift implementation can lead to more timely data collection and improved overall trial management.

Dasseti delivers innovative software solutions tailored for the due diligence and oversight of asset and fund managers. By integrating a robust and adaptable suite of features, Dasseti streamlines the assessment of funds through tools such as a digitized due diligence questionnaire engine, an automated response flagging and scoring system, research and review management, customer relationship management (CRM), collaboration tools, workflow management, an external managers portal, and comprehensive analytics. Our mission is to empower investors and investment consultants to enhance the effectiveness of their fund due diligence and monitoring processes through the power of digitization and automation. The solutions offered by Dasseti are designed to assist a variety of clients, including investment consultants, sovereign wealth funds, pension plans, foundations, endowments, family offices, wealth managers, funds of funds, insurance companies, and banks, in selecting or overseeing managers across diverse asset classes such as equities, fixed income, hedge funds, private equity, real estate, and infrastructure projects. Ultimately, Dasseti aims to revolutionize how these entities manage their investment strategies and relationships.

VACAVA offers healthcare solutions that simplify and reduce the costs associated with managing regulatory documents for clinical trials. The reliance on manual workflows can lead to delays and the risk of losing important information whenever documents are transferred. By utilizing VACAVA's solutions, you can enhance your regulatory processes by centralizing profiles, forms, and documents in a single, easily accessible online platform. With electronic approvals in compliance with 21 CFR Part 11, documents transition smoothly throughout your workflow. User-friendly dashboards provide efficient oversight, making management straightforward. Developed in partnership with a leading clinical trial research organization, VACAVA’s Regulatory Document Management System is designed to streamline operations and significantly boost efficiency. Additionally, it is surprisingly cost-effective and can be tailored to suit your specific requirements. VACAVA’s offerings are not only flexible and scalable but also delivered through the cloud, eliminating concerns about server management, security, and data backups. This means organizations can focus more on their research and less on technical hurdles.

Our innovative Smart Protocol system is designed to infuse automation and intelligence into the design of clinical trials using artificial intelligence. This groundbreaking solution is transforming the traditional manual processes that research teams have relied on to create clinical trials. In today’s digital landscape, it is practically impossible for individuals to thoroughly analyze every detail pertinent to a decision. Furthermore, many organizations possess valuable data that often goes untapped, with documents frequently stored in repositories that lack visibility. Consequently, life science companies may find themselves making significant and expensive choices based on insufficient information. Our goal is to transition organizations like yours from a document-centric approach to a more insightful, data-driven methodology. We are redefining the research and planning of clinical trials by eliminating the obstacles that separate data from its end-users. To facilitate this, we gather extensive amounts of trial-related documents from both your resources and the public domain, so you can focus on what truly matters—delivering better outcomes for patients. By streamlining access to critical data, we empower teams to make informed decisions faster and more effectively.

Protocol First not only connects disparate locations and dismantles barriers in Clinical Research during the pandemic, but its offerings remain valuable during regular times as well. What was once viewed as optional technology has now become essential. Our solutions facilitate ongoing communication, enabling research not just to persist but to thrive and progress at an accelerated pace. Featuring a fully integrated remote monitoring tool equipped with automatic tagging, our system operates seamlessly with any EDC, anytime, and from any location. Protocol First prioritizes the integration of Sites, Sponsors, CROs, and various functional areas to create a cohesive research environment. We provide holistic solutions that tackle the numerous challenges faced in Clinical Research. The foundation of Protocol First is ensuring accuracy and proper placement of your data, which increasingly incorporates AI, NLP, and ML technologies. A critical component of utilizing AI effectively is establishing a robust structure for your data. The suite of software offered by Protocol First guarantees that data flows efficiently from patients to the FDA, maximizing the potential of data science and enhancing the overall research process. As we move forward, our commitment to innovation will continue to evolve, further amplifying our impact in the field.

DFnet is a company specializing in healthcare technology that delivers eClinical solutions such as electronic data capture, eSource, and comprehensive data management services. We enhance clinical trials globally by providing increased flexibility, improved data quality, and enhanced efficiency. Our platform allows for data collection from various sources, including paper CRFs, EDC, and other electronic systems, along with online and offline tablet entries and ePRO. You can either set up our system on your premises or utilize our secure cloud hosting options. Our advanced optical recognition technology accelerates SDV and RBM processes, significantly reducing the time required for manual data entry. Designed for optimal adaptability in multi-center studies, our web-based data capture system makes data from any source readily accessible in a centralized real-time platform. This capability ensures that researchers can make informed decisions quickly and efficiently, ultimately improving the overall conduct of clinical trials.

CSAM Studies, formerly known as MedSciNet Studies, is a robust and highly adaptable online platform that has demonstrated success in managing clinical studies and trials for two decades. This web-based environment for medical research provides an advanced suite of applications designed for the hosting, administration, and oversight of projects varying in scale and intricacy. The standard offering from CSAM MedSciNet includes all essential elements necessary to establish a fully operational study or clinical trial. Additionally, this benchmark solution is equipped with features that facilitate dynamic and interactive data entry forms, customizable workflow structures, and sophisticated capabilities for data validation, analysis, and exportation. By leveraging these tools, researchers can ensure a comprehensive and efficient approach to managing their clinical studies.

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.