Bond Health accelerates clinical trial enrollment by helping research sites find eligible patients using structured and unstructured EHR data, then streamlining outreach and scheduling workflows. Our platform reduces prescreening overhead, improves recruitment efficiency, and supports sites running multiple studies at once.

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.

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.

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!  

Harbor EDC automates the most tedious and time-consuming parts of a clinical trial. For sponsors, we build your CRFs and EDC automatically, reducing set up time from months to days. For sites, we automate the data entry for you, whether you're collecting source data on paper or electronically.

The Contract Network delivers market insights and AI to speed up the paperwork that delays clinical trials, so new treatments reach patients faster.

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

UpSite Clinical is transforming the clinical trial budgeting process through its advanced AI platform, TrialProTM.  Hundreds of research sites, site networks, academic medical centers, and protocol sponsors are accelerating study startup by using TrialPro to digitize protocols, build and price budgets, identify unbudgeted work, and perform Medicare Coverage Analysis. The result has been impressive: Significantly improving negotiating cycle times and dramatically reducing work, while improving consistency and lowering errors.

TrialPro Fair Market Value benchmarks are extremely accurate and are not only calculated by therapeutic area and study phase, but also site specific characteristics and the most current data. TrialPro delivers integrated Medicare Coverage Analysis with direct linkage to National Coverage Determinations, Local Coverage Determinations, Local Coverage Articles, and treatment guidelines. The platform supports study financial forecasting and fosters more streamlined collaboration across stakeholders.

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 nearly 60 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.