WCG is at the forefront of accelerating clinical research worldwide, serving as the trusted and preferred partner to biopharmaceutical and medical device companies, contract research organizations (CROs), research institutions, and site partners. Offering a unique combination of expertise, next-generation data and insights, and tech-enabled solutions, WCG reduces complexity and optimizes study operations and outcomes while maintaining the highest standards of human participant protection. For more than 55 years, WCG has maintained a relentless commitment to efficiency, safety, and impact, empowering clinical trials to deliver life-improving therapies swiftly. For more information, please visit wcgclinical.com or follow us on LinkedIn or X @WCGClinical.
Clinical.ly provides differentiated technological solutions to the clinical research industry, which helps research facilities focus on conducting studies as efficiently as possible. The company is dedicated to developing technology that reduces or eliminates tedious manual labor so that you can focus on both patient care and study growth. While your top priority is always the patient, the success of your business hinges on satisfying all your stakeholders.
Verily is an Alphabet health technology company focused on research, care, and public health to deliver on the promise of precision health and help people live healthier lives. A state-of-the-art clinical trial management system (CTMS), built for enterprise research sites, digitizes study protocols and eliminates siloed manual processes to enable more efficient research, higher-quality output and maximum research revenue.
CITI Program is the trusted standard in research, ethics, and compliance training. We are dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners.
DDOTS provides a software application for managing all aspects of clinical research: protocols, participants, eRegulatory, IRB, pharmacy and specimens. The application consists of 4 modules operating on the same platform, creating a seamless solution to manage research operations with maximum efficiency and productivity for users.
Your friendly clinical research experts are back! From the people who first imagined outsourcing coverage analysis as a helpful site service, we understand the current challenges of clinical research sites and are here to provide customized solutions. Whether you are needing to offload workload due to resource constraints, looking for experts to guide you through the increasingly complicated world of research, needing to reduce costs, or a combination of all three, we’re here to help!
Florence revolutionizes clinical research with Site Orchestration solutions that streamline site-sponsor collaboration and accelerate trials. Trusted by 30,000+ research teams in 90+ countries, we ensure security, compliance, and efficiency. Rated #1 on G2, Florence maximizes study capacity and inspection readiness. Explore our site-first solutions at www.florencehc.com.
The Contract Network is a legal technology company that has built the world’s first AI-powered collaborative contracting platform. The Contract Network works to foster transparency and better outcomes by providing all parties to an agreement a first-class and neutral platform to radically accelerate their negotiations and to collaboratively manage their contract compliance.
The Patient Recruiting Agency™ (TPRA) is a full-service Global Patient Recruiting & Retention Company working for Sponsors, CROs, & Investigators.
TPRA specializes in Patient-centric and Site-centric recruiting and retention support with a focus on diversity. With over 25 years’ experience, TPRA has completed hundreds of campaigns enrolling over 10,000 patients of all ages and races for more than 150 healthy, disease-specific, rare, and hard-to-reach indications in multiple languages in over 45 countries.
TPRA’s value proposition is that all services are performed IN-HOUSE, which provides TPRA’s clients with greater synergy, cost efficiency, flexibility, quicker delivery time, as well as a single point of accountability.
IN-HOUSE services include branding, content development, creative design, study material development and fulfillment, media production and placement, website development, online pre-screening technologies, & RADIUS365™ real-time online response & referral delivery, tracking, managing, and reporting system.
The most substantial attributes that differentiate TPRA from its competitors are our almost 25 years of experience, our flexibility to maneuver and execute under tight timelines, our ability to implement modifications or changes quickly, and TPRA’s scalability to easily adapt service variations to best suit any type of situation, no matter the size of program.
Whether if it is through supporting a single Site’s recruiting effort, or supporting a multi-Site, multi-country program, TPRA’s quality and pricing model makes them a leader in providing successful patient recruiting and retention solutions.
Flexible. Scalable. Experienced
TRIO-US is a network of 10+ independent oncology practices across the United States interested in providing cutting edge cancer research and care to their patients in their communities. We are focused on keeping patients close to their homes while gaining access to new therapies they may not otherwise get access. We have a long-standing affiliation with UCLA that allows us to partner with clinician-scientists to bring new therapies to patients and the global community. We partner with industry and other medical centers to help develop, execute and oversee early research projects with important scientific merit we feel contribute to the oncology community, patients, clinicians, and scientists.
Upsite Clinical is transforming clinical research site administration through its clinical trial budgeting platform, TrialPro. This tool helps sites recoup countless hours and boost profitability by automating budget line itemization from study protocols and incorporating personalized Fair Market Value (FMV) pricing recommendations based on therapeutic area, study phase, and site, while finding unbudgeted work in the protocol.
Yunu provides innovative imaging workflow and data management solutions designed to optimize clinical trial processes. By integrating advanced technologies, Yunu enables life sciences organizations to streamline imaging workflows, improve accuracy, and accelerate timelines. Yunu’s platform supports clinical trials across various therapeutic areas, offering scalability and flexibility for organizations of all sizes. For more information, visit yunu.io and follow us on LinkedIn or X @Yunu_Inc.
We partner with clinical research organizations to accelerate the operations of every employee with interpretable, reasoning based technique designed to reduce manual workflow burden and enhance internal expertise.