eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert biometrics services and the elluminate Clinical Data Cloud – the foundation of digital trials. Together, the elluminate platform and eClinical Biometrics Services give clients self-service access to all their data from one centralized location plus advanced analytics that help them make smarter, faster business decisions.

For over 25 years, ScienceMedia, a protocol compliance management company, has been at the forefront of delivering innovative, multimedia learning solutions aimed at improving clinical competency across all functional areas in the world's leading Life Sciences organizations. ScienceMedia delivers science and medical training that will engage your people. Visit ScienceMedia's YouTube channel to learn more. Request a free demo of SMi Trial.

Bioforum offers a wide range of consulting, data management, and biostatistical services to help your clinical trial succeed and get accredited. Our interdisciplinary team of medical writers, clinical data managers, programmers, and statisticians has the experience and flexibility to provide customized, proactive support for all projects and programs, whether small and highly specific or large and complex.

From specialty biotechs to multinational pharmaceutical companies to nonprofits and academic medical centers, we partner with clients across the clinical trials continuum, from start to finish. Our approach is to provide scalable solutions based on the specific needs of each client.

Introducing BioGrid; The most effective way to graphically represent data-driven insights, BioGrid is an intuitive and easy-to-navigate analytics and visualization platform.

Medidata is leading the digital transformation of life sciences, creating hope for millions of patients. Medidata helps generate the evidence and insights to help pharmaceutical, biotech, medical device, and diagnostics companies, and academic researchers accelerate value, minimize risk, and optimize outcomes. More than one million registered users across 2,000+ customers and partners access the world's most trusted platform for clinical development, commercial, and real-world data. Medidata, a Dassault Systèmes company (Euronext Paris: FR0014003TT8, DSY.PA), is headquartered in New York City and has offices around the world to meet the needs of its customers. 

With over 15 years of experience in conducting early-phase clinical trials for Biotechnology and Pharmaceutical companies, Nucleus Network understands the evolving landscape of drug development. Access to patients, shortened recruitment timelines, and the evolution of pharmacodynamic (PD) biomarkers are key fundamentals underpinning Nucleus Networks' multi-country, multi-site approach to Phase 1 clinical trials.

Nucleus Network White Paper Streamlining Early Phase Development

Sponsors are increasingly off-shoring Phase 1 trials due to opportunities for cost reduction, improved timeline, increased quality, and additional market entry opportunities. Review the whitepaper to understand regulatory differences, speed benefits, and how to maximize Phase 1 value inflection.

Clario is a leading healthcare research and technology company that generates the richest clinical evidence in the industry for our pharmaceutical, biotech and medical device partners. Across decentralized, hybrid, and site-based trials, our deep scientific expertise, global scale, and the broadest endpoint technology platform in the industry allow our partners to transform lives. Clario’s eCOA Digital Solutions has been powering hybrid and decentralized clinical trials (DCT) for over 20 years, enabling sponsors to collect high-quality endpoint data from any modality or location, all while improving the patient experience and diversity. Clario has the only technology platform that combines eCOA, cardiac safety, medical imaging, precision motion, and respiratory endpoints. With 30 facilities in nine countries, Clario's global team of science, technology, and operational experts has helped deliver over 19,000 trials and 870 regulatory approvals for over five million patients in 120 countries. Our innovation has been transforming clinical trials for 50 years. 

August Research is an American-owned, boutique CRO focused on clinical trial operations across Europe. From Spain to Georgia, we are your 'high-touch' partner for successful clinical trials in Europe.

CluePoints provides Sponsors and CROs a better way of detecting and managing risks that may impact the outcome of clinical trials. Our solutions, all of which are underpinned by Central Statistical Monitoring, a technique that’s being investigated by the FDA for selecting sites for inspection, are deployed to drive a Risk-Based Quality Management strategy, as advocated by ICH and FDA.

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 22,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators, and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years are moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With people, insight, and focus on operational excellence, we work With Heart^TM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference.

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At Worldwide, we believe a personalized approach is the only way to unlock the power of everyone working on a study – from operational and therapeutic experts to site partners and scientists. That means you’ll always have direct access to our experts. You’ll be able to tap into more than 30 years of therapeutic experience on a global scale. And your mission is our mission – we are dedicated to working with you to meet your goals.

Case Study: Executing With Speed and Quality Operational & Strategic Excellence in the Delivery of a Global Phase III Trial

YPrime has more than 10 years of experience designing cloud-based technology solutions to meet the needs of today’s complex challenges while innovating for tomorrow’s clinical trials. From designers and developers to managers and support techs, our seasoned team works with one goal in mind: Ensuring an optimal experience 
for sponsors, sites, and patients. Our interactive response technology (IRT) and electronic clinical outcome assessment (eCOA) platforms, clinical supplies consulting, patient engagement, and decentralized clinical trial (DCT) solutions help expedite and improve the quality of patient management, supply chain management, drug accountability, and clinical data. Our scientific staff help clients focus on those endpoints and timepoints that answer the most important research questions and meet regulatory expectations. Our data science team optimizes the technology to drive better outcomes and deliver the highest quality data. Our data services and tools help sponsors bring together fragmented clinical research data into contextual information they can act on. YPrime’s technology and service offerings enable sponsors to move faster and more efficiently to their next development milestone. We’re here to help you make a positive impact by bringing life-changing therapies to market

Stiris Research Inc. is an entrepreneurial Clinical Trial Management Company, providing comprehensive study management solutions for Phase I through Phase IIIB clinical research. We provide tailor-made services from full-service outsourcing to focused clinical study management.

Science 37 Holdings, Inc.’s (Nasdaq: SNCE) mission is to accelerate clinical research by enabling universal trial access for patients. Through our Metasite™ we reach an expanded population beyond the traditional site, delivering on our goal of clinical research that works for everyone—with greater patient diversity. Patients gain the flexibility to participate from the comfort of their own homes, at their local community provider, or at a traditional site when needed. Our Metasite is powered by a proprietary technology platform with in-house medical and operational experts that drive uniform study orchestration, enabling greater compliance and high-quality data. To learn more, visit www.science37.com, or email science37@science37.com. Visit Science37 Vimeo to learn more about the services their team offers.

Greenphire’s suite of best-in-class technology solutions enables clients to prioritize the patient journey, so treatments and cures can be delivered to those who need them faster. Committed to modernizing and integrating each step in the participant journey and the overall clinical trial lifecycle, Greenphire has established an unmatched suite of patient convenience solutions, including a mobile-enabled technology platform that offers a personalized and empowering end-to-end participant experience from trial identification (patient registry) through participation. ClinCard® and ConneX® remove financial and logistical barriers, simplifying the delivery of global patient convenience initiatives and improving recruitment and retention. Greenphire’s EnvisiX™ and eClinicalGPS® transform the budgeting and site payment process, resulting in expedited study start-up and improved site sustainability.

Faro Health is bringing clinical trials into the digital age by helping teams manage and balance the complexity of modern trial designs through a cloud-native platform. The Faro platform enables study teams to design complex clinical trials using small modular building blocks and combines that with data-driven insights to orchestrate and automate operationally complex trials. Faro brings balance, centricity, and flexibility to protocol development through automation and integration to downstream systems and vendors, ensuring they are always up to date, and correctly configured. As a result, clinical trials using Faro are operationally efficient which avoids delays due to ambiguity and generates data that can be trusted. Watch here to learn more about Faro Health.