Advanced Monitoring Methods offers quality monitoring, data collection, compliance, and environmental consulting services.

BioMerieux designs, develops, manufactures, and markets in vitro diagnostic systems for clinical and industrial applications. The company’s diagnostic systems consist of reagents and consumables used to conduct biological tests, for use in performing screening, diagnostic assistance, prognosis, and treatment monitoring; instruments, platforms, and autoanalyzers used for automated testing at high or low throughputs; software to process analyses and systems to interpret biological test results; and other related services such as the installation and maintenance of instruments, user training, and the audit of laboratory workflows. BioMerieux offers diagnostic systems for clinical applications including the diagnosis of infectious diseases, comprising HIV, tuberculosis, and respiratory diseases, as well as cardiovascular diseases and targeted cancers based on the analysis of biological samples such as blood, saliva, and urine; and for industrial applications including the analysis of microbiological manufacturing such as food, pharmaceuticals, and cosmetics. The company markets and sells its products through a network of distributors to private sector analysis laboratories, hospital laboratories, blood banks, and physician office laboratories; food, pharmaceutical, and cosmetics industries; and independent quality control laboratories. It has operations in Europe, the Middle East, Africa, North America, Asia-Pacific, and Latin America. BioMerieux were founded in 1963 and is headquartered in Marcy l’Etoile, France. It is a subsidiary of Institut Mérieux.

Medidata is an unified life science platform. They help generate the evidence and insights to help pharmaceutical, biotech, medical device and diagnostics companies, and academic researchers accelerate value, minimize risk, and optimize outcomes. Their products and solutions include clinical cloud, patient cloud, decenteralized clinical trials, and more.

Frontier is a software application service provider that delivers end-to-end applications and data management solutions for the Life Sciences Industry. The company was founded in 2013 and is headquartered in Blue Bell, Pennsylvania.

Castor is an international health-tech company founded by CEO Derk Arts, MD, Ph.D. Their cloud-based clinical data platform simplifies the entire clinical trial process, from recruitment to analysis, for researchers worldwide. More than 50,000 researchers across 90 countries are using Castor to supercharge their research. Castor’s platform has supported more than 4,000 commercial and academic studies that cover a broad range of therapeutic areas including diabetes, cardiovascular disease, rare diseases, infectious diseases, and oncology. Researchers on the platform generate vast amounts of data from traditional and remote trials, and Castor recently reached milestones of 180,000,000 data points and 2,000,000 enrolled patients. Castor’s goal is to make the world’s research data reusable, enabling AI-driven clinical trials, and ultimately creating a future in which they maximize the impact of data through reuse.

Triall brings Web3 to medical research by creating a digital ecosystem of blockchain-integrated software solutions that secure and streamline clinical trials. Triall’s solutions make clinical trials tamper-resistant and enable secure and efficient integrations between the many isolated systems and parties involved in clinical trial processes. Triall’s software is co-created with clinical trial professionals to ensure optimal user experience, solving actual industry pain points.

ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialise in the strategic development, management and analysis of programs that support Clinical Development - from compound selection to Phase I-IV clinical studies.

Syneos Health® (Nasdaq:SYNH) is the only fully integrated biopharmaceutical solutions organization. The Company, including a Contract Research Organization (CRO) and Contract Commercial Organization (CCO), is purpose-built to accelerate customer performance to address modern market realities. We bring together approximately 24,000 clinical and commercial minds with the ability to support customers in more than 110 countries. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients.

Provider of medical informatics system intended to enhance data quality, flexibility, and real-world evidence. The company's platform integrates clinical trials, medical devices, and real-world data collection, enabling healthcare professionals to access relevant patient, hospital, and real-world data for informed decision-making.

Simplified Clinical provides world class clinical trial software as a service (SaaS). Their belief is that web-based CTMS software should be simple and affordable. Their Clinical Discovery Platform (CDP) provides an intuitive, compliant solution allowing investigators, clinicians, and data managers to perform their roles accurately and efficiently. Their products and services have been and will continue to be a reflection of the needs of their clients and their investigational partners. They believe that when it comes to information systems, simpler truly is better. Their unwavering commitment to this guiding principle is demonstrated in their name, and in their Clinical Discovery Platform℠. They have conducted extensive field-based research, which included one-on-one interviews, Focus groups, and hands-on system usability testing. As a result, they have concluded that the specific goals of their clients and investigational end users can best be met through the development, maintenance, and delivery of simplified clinical data systems.

Curavit is a “virtual CRO”, purpose-built to design and execute decentralized clinical trials. The company works with our clients to design their trials from first principles, based on the team’s decades of experience in research and digital health technologies. For each trial, they assign an experienced principal investigator, who is an expert in the specific disease area, to develop the protocol and drive the regulatory submission process. Curavit manages participant recruitment, enrollment, and consent. Under the direction of the PI, their clinical study team executes the entire decentralized clinical trial.

Trialize is an AI-driven clinical trial automation platform that dramatically accelerates timelines, cuts costs, and ensures real-time data insights to reduce the risk of missing endpoints.

IQVIA is the result of the 2016 merger of Quintiles, a leading global contract research organization, and IMS Health, a leading healthcare data and analytics provider. The research and development segment focuses primarily on providing outsourced late-stage clinical trials for pharmaceutical, device, and diagnostic firms. The technology and analytics segment provides aggregated information and technology services to clients in the healthcare industry, including pharmaceutical companies, providers, payers, and policymakers, as well as data and analytics capabilities for clinical trials, including virtual trials. The company also has a small contract sales business.

Science 37 is making the promise of virtual trials the new reality. By engaging with patients from the comfort of their own home, the company provides access to patients who can never be reached by traditional site-based research models. Its virtual model has proven to enroll faster, retain patients at a higher rate, and reach a more representative patient population. Science 37 has conducted more virtual (or decentralized), interventional trials than any other company, using an expansive, in-house network of telemedicine investigators and home-health nurses. The company's research is powered by the industry’s most comprehensive, fully integrated clinical trial platform purpose-built to conduct virtual trials.

Veeva Systems is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence and customer success, Veeva has over 400 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs. Founded in 2007, Veeva is a publicly held company headquartered in the San Francisco Bay Area, with offices in Philadelphia, Barcelona, London, Paris, Beijing, Shanghai and Tokyo. For more information, visit www.veevasystems.com

Developer of a precision research clinical platform designed to bring therapeutics to market. The company provides an infrastructure to reduce the complexity of distributed trials that includes new site activation and site monitoring, enabling investigators and patients to facilitate and optimize clinical research.

Adaptive Clinical Systems™ is an eClinical Technology Solutions provider and “Problem-Solver” providing EDC to CTMS integration and data flow improvements in your clinical trials. Through their innovative Adaptive eClinical Bus® solution, their focus is on helping improve clinical trial operations through interoperability. The Adaptive eClinical Bus® gives their clients the freedom to choose the best eClinical tools of any third-party or proprietary systems while enjoying the benefits of a fully integrated system. The Adaptive eClinical Bus includes “connectors” for leading clinical trial software from well-known vendors such as BioClinica, Medidata, and Clinical Conductor; open source clinical trial tools such as OpenClinica and Clinovo; and popular EMR/EHR tools from EPIC, PointClickCare, and others.

Acceliant offers eClinical trials solutions to global contract research organizations, pharmaceutical and medical device enterprises Acceliant is a preferred partner of global contract research organizations (CROs), pharmaceutical and medical device enterprises for e-Clinical trials solutions and services. Our journey coincides with the origin of the e-Clinical trials industry. Our expertise and long-term relationships with sponsors help us shape the next-generation e-Clinical suite of solutions.

Modern Trials provides electronic healthcare data to identify patients in need of advanced treatment options. They offer services that include emr-integrated participant identification, participant screening, a clinical trial management system, and non-trial emr data monetization.

Vitalliance Corporation is a pharmaceutical supply chain management and analytics company. The service includes Humanitarian aid network, logistics management solution, and Africa support center. The company offers customer support through email.

Bloqcube is an innovative company built an integrated clinical trial management and financial system. It automates processes, optimizes intermediaries, and integrates siloed systems. The company delivering innovative solutions to address inefficiencies in the pharmaceutical value chain for the benefit of patients. Bloqcube also built on an iPad with one-time electronic data entry, which helps to take the trial to the patient in order to facilitate greater access by patients who are unable to travel to sites. Both financial and patient activity data are delivered in real-time, and the use of blockchain enhances data integrity in order to ensure more secure storage of information and minimizes the vulnerability to malware attacks. Bloqcube was founded in 2017 and is headquartered in Piscataway, New Jersey, USA.

YonaLink is a global network of over 30,000 medical centers that provides EHR-to-EDC streaming and AI-driven CRF data mapping. YonaLink collects clinical trial data in real-time, improves trial efficiency and data quality, reduces medical center staff burnout, and provides wider access to novel patient care opportunities.

Developer of drug discovery management platform designed to provide convergence between IT services for clinical trials. The company's platform features the ability to provide image data management during clinical trials, data warehousing for accumulated data of completed trials, case review and medical monitoring during clinical trials and more, enabling healthcare companies to manage their drug discovery pipeline for both ongoing trials and completed trials.