A family-owned company, bioMérieux has grown to become a world leader in the field of in vitro diagnostics. Our entrepreneurial adventure, begun over a century ago, is driven by an unrelenting commitment to improve public health worldwide. Since 1963, we've been paving the way in the field of in vitro diagnostics and have contributed greatly to improving public health and making the world a healthier place. The solutions that our teams imagine, develop and manufacture are key to enable healthcare professionals and industry players to make confident decisions to improve patient outcome and ensure consumer safety.

Operator of a comprehensive software and data analytics system platform intended for the process of clinical research. The company's platform integrates functions for clinical data management, encompassing advanced electronic data capture and standardization tools, as well as core clinical operations features like site monitoring and electronic trial master file management, enabling biopharma organizations to accelerate study timelines, improve data quality, and drive smarter global clinical studies.

Most healthcare CRMs are retrofitted sales platforms that create more problems than they solve. At Frontier-IQ, we built intelligent healthcare CRM for life sciences that eliminates inefficiencies without adding complexity. Our Solutions: + Patient-Focus™: Smarter patient CRM that empowers support teams to help patients faster—from insurance verification to medication access—without gaps, delays, or unnecessary steps. Featuring configurable workflows, mobile-optimized interfaces, and seamless EMR integration. + Clinical-IQ™: Streamline clinical trials with real-time tracking, automation, and compliance tools that reduce inefficiencies and keep research moving forward. Includes predictive analytics that anticipate and prevent potential bottlenecks before they occur. + Data-IQ™: Transform healthcare data into clear, actionable insights that drive smarter decisions by breaking down data silos. Our AI-powered platform connects disparate data sources and delivers personalized insights without requiring data science expertise. Why Frontier-IQ for Life Sciences CRM: • No Hidden Fees. No Overcomplication. Just Smarter Healthcare. • Designed for Efficiency. Built for Real-World Impact. • Proven ROI—More Value, Less Wasted Time. • Configurable by Your Team, Not IT: Make changes in minutes, not months. Discover how our patient CRM helps life sciences teams streamline workflows, improve patient outcomes, and drive measurable results. Schedule a demo or request more information to see how our solutions can make a difference for you. Explore the frontier of patient-centric innovation. Visit our website (www.frontier-iq.com) to learn more. Frontier-IQ: UNIFYING HEALTHCARE: PATIENTS, DATA, RESULTS

At Castor, we believe in the power of clinical research and the power of technology. And we know that together, these forces can help extend human healthspan. To achieve this reality, we must make patient-centered clinical trials a possibility for everyone, anywhere in the world. That's why we are using technology to capture the world's research data and optimize each activity of a clinical trial. From recruitment to monitoring, our modular clinical trial platform makes it easier to design and deploy trials, enroll and engage patients, collect data and analyze results. Each module can be used individually or in unison with others, providing the ability to customize each solution to fit your needs, and grow at your own pace. That’s delightful for patients, effortless for study teams, risk-free for sponsors.

Triall offers the technology, tools, and expertise to drive your clinical development forward. We empower clinical research professionals throughout the full clinical trial lifecycle—from study design, to execution, and post-study activities. CIX (coming soon) Triall’s Clinical Insights Exchange (CIX) provides data-informed insights for study design and planning by applying privacy-enhancing technologies to analyse historical clinical trial data. eClinical solutions Triall offers an interoperable suite of eClinical solutions that can be configured to your unique study needs. Our platform includes advanced web-based, mobile, and wearable integration capabilities to support decentralised, hybrid, and centralised clinical trials. CRO services Triall has built a network of selected CRO partners that each excel in their respective domains, allowing us to offer you a truly end-to-end service offering that covers all key aspects of clinical trial design and execution. Want to elevate your clinical trials to new heights? Check out our website or reach out to our team at contact@triall.io

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, commercial and real world insights into outcomes to address modern market realities.   We bring together a talented team of professionals with a deep understanding of patient and physician behaviors and market dynamics. Together we share diverse insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. Syneos Health is powered by an authentic, inclusive and high-performance culture that cares for colleagues, customers, patients, communities and the environment.

Wemedoo is a clinical technology company built on deep clinical research expertise. We specialize in unified Clinical Research Information Systems (CRIS). Our clinical trial software, oomnia, unifies Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), Randomization and Trial Supply Management (RTSM), electronic Informed Consent (eConsent), electronic Source (eSource), electronic Patient-Reported Outcomes (ePRO), and electronic Clinical Outcome Assessment (eCOA) into one interoperable solution. By replacing fragmented platforms with a unified data model and shared governance layer, Wemedoo makes clinical research faster and smarter while ensuring 100% oversight, full data traceability, and continuous regulatory compliance at all times. We support sponsors and CROs conducting clinical trials of any size, design, or geographic scope, from single-country and decentralized studies to large, global programs, all requiring structured data, inspection readiness, and complete operational control without system fragmentation.

Historically a boutique provider of hosted clinical data management systems to a limited number of “referral only” clients, Simplified Clinical has become a leader in EDC/CDMS software solutions. This leadership role has been made possible by combining a successful 20-year track record and a strategic partnership with Microsoft and their Azure/Cloud for Healthcare. Our belief is that web-based CTMS software should be simple and affordable. Our Clinical Discovery Platform (CDP) provides an intuitive, compliant solution allowing investigators, clinicians, and data managers to perform their roles accurately and efficiently. Our products and services have been and will continue to be a reflection of the needs of our clients and their investigational partners. Our staff and partners are made up of industry veterans in the fields of clinical, regulatory, data management, and information systems development. The team has been assembled in order to help research organizations reduce and control the costs associated with performing clinical trials, while increasing the speed with which clinical trial data is collected, processed and made available for meaningful analysis. We believe that when it comes to information systems, simpler truly is better. Our unwavering commitment to this guiding principle is demonstrated in our name, and in our Clinical Discovery Platform℠. We have conducted extensive field-based research, which included one-on-one interviews, Focus groups, and hands-on system usability testing. As a result, we have concluded that the specific goals of our clients and investigational end users can best be met through the development, maintenance, and delivery of simplified clinical data systems. Feel free to contact us to explore our on-line CDP Demo, for answers to any questions you may have, or to discuss options for your next clinical study.

We fix the execution layer of clinical trials. Clinical trials rarely fail because of science—they fail because of execution. Enrollment delays, fragmented participant management, and incomplete data continue to slow timelines and increase risk. Curavit is a Clinical Research Organization (CRO) and Remote Clinical Site purpose-built to address these challenges. We enable sponsors to recruit, enroll, and manage participants at national scale. All while working seamlessly alongside existing CROs, sites, and study infrastructure. Our model improves what matters most: *Faster, more predictable enrollment *Better participant engagement and retention *High-quality, longitudinal data collection

Trialize cuts the biggest operational pain‑points in clinical trials. It turns the slowest, most error‑prone parts of trial operations into automated, real‑time workflows — compressing timelines and boosting data quality in one step.

IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.

Science 37 is a clinical research site that delivers trials directly to patients' homes. We accelerate research by expanding patient access to trials, leading to faster approvals and better health outcomes for all. Our solutions empower life sciences companies to reach diverse populations beyond traditional means of conducting clinical research. To learn more, visit www.science37.com or email science37@science37.com.

Veeva MedTech enables medical device and diagnostic companies to streamline the complete product development and commercialization lifecycles to deliver products to patients with greater speed and efficiency. Veeva MedTech’s offering includes applications that advance clinical, regulatory, quality, commercial, sales, and medical operations.

Macro Trials is the precision research clinical platform, driving increased research velocity and an amplified patient experience to unlock value for all stakeholders in the clinical trial ecosystem. Via its digitally powered infrastructure and "hub-and-spoke" distributed model, Macro partners with pharmaceutical companies, CROs, providers, and health systems to conduct trials for high-value therapeutics. The company’s turnkey platform empowers physicians to participate in groundbreaking research via workflow-native efficiency tools, clinical research personnel and a network of logistic partners. Macro’s clinical trial intelligence platform and proprietary real-world evidence as a service (RWEaaS) product supports life sciences companies in all aspects of therapeutic research, development, and commercialization.

Adaptive Clinical Systems, a global life sciences technology company, offers a simple, secure, validated, compliant and cost-effective solution for data interoperability as well as reporting and visualization for clinical trials. Adaptive Clinical offers the Adaptive eClinical Bus and Adaptive DataVIEW. The Adaptive eClinical Bus®, a cloud-based hosted service, will integrate with any EDC, eCOA, CTMS, ePRO/IWRS, Medical Imaging, IRT, Analytics, Data Acquisition Systems as well as RWD, EHR/EMR to reduce error and speed data management for any size study. With the Adaptive eClinical Bus, patient- centric clinical trials can ensure interoperability and full compliance from the many diverse eSources generated from the explosion of data from Digital Health Technologies (DHTs), such as wearables and remote patient monitoring (RPM) solutions. Key benefits of the Adaptive eClinical Bus include: ✔️ Fully-validated Platform with Detailed Audit Logs and Reports ✔️ Fully compliant with HHS 45 CFR Part 64, FDA 21 CFR Part 11, GxP and other regulatory guidelines ✔️ Standards-based for Interoperability ✔️ Easily Implement an eSource Data Capture Workflow ✔️ Adaptive Rules Engine offers Built-in Clinical Intelligence ✔️ Reusable components for Quick Installation ✔️ Full training and 24/7 support Adaptive DataVIEW provides a robust solution for visualizing and analyzing data from disparate sources quickly and efficiently. It provides real-time, bi-directional data from many disparate sources into comprehensive dashboards. Purpose built for clinical trial operational key performance indicators and dashboards. Reports can be created at the patient, site, study or program level, including across studies. Adaptive DataVIEW enables “single click-back” from any widget or dashlet to the data source regardless of eClinical tool.

Acceliant provides real-time, integrated clinical trial solutions for life sciences, CROs and pharma tools and expertise to take intelligent and smarter decisions. Its eClinical Suite allows users to build studies, design electronic case report forms (eCRFs), capture data through multiple sources (EDC), capture data directly from patients (ePRO), and manage other clinical data management functions. A pioneer in the EDC industry, Acceliant has been providing solutions in the clinical trial management space to the industry since 1999. Since then, Acceliant has served customers in the CRO, medical device, pharmaceutical, biotech, and non-profit drug research industries. The Acceliant eClinical Suite has helped facilitate clinical data management in hundreds of trials for global giants as well as emerging healthcare innovators.

Modern Trials partners with healthcare organizations and leverages electronic healthcare data to identify patients in need of advanced treatment options and match them with appropriate clinical trial opportunities in a patient-first and HIPAA-compliant manner. Warm handoffs are used to refer qualifying patients to contract research organizations for trial enrollment on a subscription + fee-for-service basis and ongoing support is provided to patients through trial participation. Modern Trials extends the ability of healthcare organizations and physicians to offer the most cutting-edge treatments available, we bring potentially life-saving therapeutics to patients in need and we help our customers, life science organizations, save $billions by filling their clinical trials with more representative samples faster and cheaper than ever before, reducing time-to-market for new therapeutics. Modern Trials is thrilled to announce our inclusion as an ARPA-H CXHub member and the launch of our Trial Recruitment Toolbox SaaS offering in 2024!

Emerging countries face the daily challenge of getting the right medical supplies, treatments & vaccines, to the right people, at the right time. The role of Vitalliance is to help simplify the complexity of the healthcare supply chain in order to improve patient outcomes. Vitalliance combines international public and private sector healthcare expertise with industry leading supply chain technology to maximize product availability, quality, and affordability. This shared goal is accomplished through collaboration and partnerships with Donor Organizations, Ministries of Health, Pharmaceutical Suppliers, Faith-Based, Philanthropic, and Private Sector organizations. The Vitalliance Health Network facilitates collaboration across a universal platform with complex supply chains that extend to all constituents. It provides essential secure sharing of information and real-time visibility across a mutual network for healthcare supply chain participants to plan, forecast, track, and execute more accurately. This cumulative solution has an exponential benefit in improving medical supply availability and improved patient outcomes.

Bloqcube is an innovative clinical trial management and financial systems software company dedicated to accelerating clinical research with integrity across Hybrid and Decentralized trial models. The company is redefining traditional cost structures through intelligent, secure, and integrated digital infrastructure. Recognized for innovation and industry impact: • 2019 PM360 Innovators Award • 2021 CIO Award • 2022, 2023, 2024, 2025 Prix Galien USA Nominee - Startups in Digital Health • 2022 UCSF Digital Health Rising Stars Nominee • 2022 PM360 Innovators Award for BloqBridge, Bloqcube’s Supply Chain Management (SCM) service • 2023 ConV2X Pitch competition winner

Yonalink provides EHR-to-EDC streaming and AI-driven CRF mapping along with other clinical trial data management solutions. Yonalink eliminates the manual work involved in clinical data capture to guarantee secure, error-free data collection from EHR to EDC. By collecting and transfering clinical trial data in real-time, Yonalink improves trial efficiency and data quality, reduces medical center staff burnout, and provides wider access to novel patient care opportunities.

We are Trial Informatics (TI), a Data Science company founded by a group of experienced medical doctors, health scientists, IT professionals, and data scientists in South Korea with the vision to reinvent clinical trial data with digital health technologies. Our mission is to digitalize clinical trial processes by capitalizing on Data Science, thereby supporting medical doctors, clinical researchers, contract research organizations (CROs), pharmaceutical companies, and other stakeholders to succeed in a clinical trial, small or large, with the state-of-art IT technologies and Data Science tools at every important stage of clinical development. Our solutions aim, among others, to streamline clinical research process, integrate data workflows of various stages, warehouse clinical trial data in a standardized manner, uncover new insights from past data, and serve as a digital platform for Decentralized Clinical Trials (DCTs). We have two child companies, TI Image and iAID. TI Image (https://tiimage.com), headquartered in Singapore and led by Dr. Amy Lee, is a global imaging CRO providing, most importantly, the central reading service for imaging clinical trials end-to-end on all the major therapeutic areas. iAID (https://iaidimage.com), headquartered in South Korea and led by Dr. Jeongjin Lee, is an AI company specializing in the AI medical imaging process, with invention of a high-speed web-PACS, which is now widely employed by the leading hospitals and medical research labs in South Korea. Contact: cs@trialinformatics.com

What is TrialX? TrialX is a clinical research and space health informatics company headquartered in New York City. From launching the first clinical trials app on Google Health in 2008, to powering online patient recruitment and research data collection for space missions, TrialX is empowering clinical research here on earth and beyond. Our Solutions: Enterprise Patient Recruitment: With our award-winning patient recruitment management platform – we are helping thousands of patients find relevant trials and get connected to research teams seamlessly. Recently, we announced the launch of a new Diversity, Equity and Inclusion (DEI) toolkit in the platform – that will have a wide ranging impact by bringing diversity and inclusion in the front and center of patient recruitment workflows. Our platform serves as a central system for patient recruitment operations at major pharmaceutical sponsors, large academic research centers and patient advocacy groups, which includes a clinical trials finder, study website builder, pre-screeners, referral tracking, volunteer registry and real-time analytics. Remote Data Collection: TrialX's fully scalable end-to-end Remote Data Collection platform powers hybrid/virtual global clinical trials. Clinical trial teams can manage both sites and patients within the system. Key features include eConsent, Pre-screeners, eCOA/ePRO, Cognitive Tasks, Virtual Visits, Push/SMS Reminders, Wearable Integrations, and a powerful analytics dashboard to monitor participants and unlock insights. Online Talk Shows: CureTalks raises clinical trials awareness by bringing patients, patient advocates and researchers on the same platform. Visit trialx.com to learn more.

WHAT WE DO: Mosio enables clinical research teams to improve patient adherence, communications, and data collection on mobile’s most popular channel: text messaging. If you're finding, like other researchers, that phone calls and email isn't getting the job done, it's time for text messaging, which can be automated, personalized, and easily integrates with third party clinical trials software like EDC, CTMS, ePRO, or eCOA. Study sponsors, CROs, Principal Investigators, and research teams use Mosio to improve patient engagement, retention, and data collection efforts with interactive mobile messaging. Our software makes research teams more efficient in how they communicate with study participants through messaging automation and interactive elements delivered to participant mobile phones. WHO WE HELP: ✅ Clinical Trial Sponsors (Pharma and Biotech) ✅ Cancer Centers and Clinical Research Organizations ✅ NIH-Funded Studies ✅ Clinical Trial Managers, Clinical Operations Managers/Directors, Clinical Project Managers, Principal Investigators, Clinical Research (Study) Coordinators, and any research staff who communicate regularly with study participants. BENEFITS: ➕ Interactive dosing reminders and medication adherence alerts. ➕ Automate data collection. ➕ Increase engagement and adherence. ➕ Fix your no-show problem with SMS appointment reminders. ➕ Improve retention with automatic coordinator check-ins and motivational messaging. ➕ Efficiently communicate via two-way text messaging automatically, or in real-time. ➕ Pre-schedule personalized survey questions or messages based on individual participant timelines. GET IN TOUCH: Capabilities: https://www.mosio.com/capabilities Pricing: https://www.mosio.com/get-pricing