Greenphire Signs Enterprise Agreement with Top 20 Biopharmaceutical Company
KING of PRUSSIA, PA (June 25, 2012) – Greenphire, the leading provider of clinical payment technology and service solutions to Biopharmaceutical and medical device companies, today announced it has signed a 5-year enterprise agreement with a top 20 Biopharmaceutical Sponsor for its eClinicalGPS solution.
The eClinicalGPS solution will allow the Sponsor to fully automate the calculation, approval and execution of payments to clinical research sites in over 200 countries in local currency. The solution will be deployed across all new and existing studies. Beyond the immediate need to more effectively manage the payment process, improve efficiency, reduce costs and provide a single source for clinical financial analytics, the solution also provides the platform on which to aggregate all site payment in preparation for the compliance requirements of the Sunshine Act and related international transparency regulation.
Greenphire Co-founder and Chief Executive Officer Sam Whitaker, commented, “this agreement represents the beginning of a significant change in the way Sponsors think about the payment process within the clinical trial environment. Our vision of applying well designed, automated and scalable technology to a process which has historically relied on manual processes is driving positive change. We are reducing administrative burden, reducing payment cycle times and improving accuracy.”
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.
