CFS Clinical (CFS) achieved a significant milestone of $700 Million in site payments issued – a number that continues to grow as pharma drives to accelerate trials and comply with the latest Sunshine Act legislation. Since its inception, CFS has been perfecting its first-to-market solutions to solve the number one issue among doctors participating in clinical research – getting paid timely to improve cash flow. Not only do better payment processes promote research for new medicines, but also the Centers for Medicare & Medicaid Services (CMS) Sunshine Act, now known as “Open Payments,” is mandating transparency with a national program for these payments. While the Open Payments program has created significant challenges for the industry, it is also disrupting antiquated payment processes and forcing the adoption of better practices for keeping clinical trials a viable business model for physicians.
CFS’s methodology to this complex payment process entails a highly controlled and fully integrated global payment environment, which improves pharmaceutical sponsor compliance with the U.S. Federal Open Payments, state, and growing global aggregate spend reporting requirements. Moreover, the process drives physician’s satisfaction and ability to participate in research, which is critical to bring new drugs to market. As the market leader, CFS is also the only company in its space with a SSAE16 SOC 1 Type II report for its investigator site payment processing environment.
“Reaching this milestone of nearly three quarters of a billion dollars in investigative site payments is exciting for us, but we’ve only just begun,” comments Greg Seminack, President and Managing Partner of CFS Clinical. “The advent of the TransCelerate initiative is proof of the industry’s desire to drive positive disruptive change, and CFS is well positioned with a core competence in transforming the business and financial management of trials.”
The team of CFS experts leverages its technology platform, CFS Payment InSite™, to issue payments electronically to sites on behalf of pharmaceutical sponsors around the world, efficiently and accurately. In addition, CFS supports its clients by navigating the global tax complexities and contractual considerations inherent in the process – an essential service when dealing with the 40+ countries in CFS’s current portfolio.
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.
FDA-Approved Gene Therapy Beqvez Shows Sustained Efficacy, Safety in Long-Term Hemophilia B Trial
April 17th 2025Beqvez (fidanacogene elaparvovec), an FDA-approved one-time gene therapy for hemophilia B, demonstrated sustained factor IX expression, low bleeding rates, and a favorable safety profile over long-term follow-up.