CFS Clinical Exceeds $700 Million in Clinical Trial Site Payments
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.
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