Princeton, NJ-The Avoca Group today announced a new platform to accelerate the prequalification of clinical service providers by leveraging analytics-driven technology and industry-leading standards to provide rapid, intelligent access to in-depth RFI questionnaires. The Diligent™ Prequalification Platform furthers the work Avoca has become known for over the past 20 years, and reinforces its mission to transform the clinical trial execution process by bringing efficiency, quality, and risk mitigation to the forefront. “The Diligent Platform centralizes prequalification information, which we believe will transform how the industry approaches this process,” says Patricia Leuchten, CEO, The Avoca Group. “The current methodology for prequalifying and selecting vendors is redundant and dysfunctional. By combining the Avoca Quality Consortium’s industry-accepted standards with an intelligent technology platform, we are able to offer business process transformation by shortening timelines for clinical trial execution. The offering enhances quality, mitigates risk and increases compliance. This is the first stage of a comprehensive technology roadmap.” Purdue Pharma, Sanofi, and Seattle Genetics have committed sponsorship to support development of the technology. In addition, the sponsors will direct the expansion of Diligent beyond its current focus on endpoint generating technical services and into more functional CRO service categories including, data management, field monitoring, and biostatistics. “The Diligent platform is a powerful solution to streamlining the prequalification process and supporting companies in making the best decisions while maintaining compliance,” says Marie Anne Stager, Vice President, Clinical Development Operations, Seattle Genetics. “The platform affords companies the opportunity to better utilize technology to enhance clinical trials processes.” The Avoca Group welcomes CROs and other types of service providers to join this select group of Diligent sponsors. The support and input of other clinical research providers adds value to the offering and future developments of Diligent. For information on becoming a sponsor, contact [Dennis Salotti at dennis.salotti@theavocagroup.com]. Link to Diligent RFIs: http://theavocagroup.com/diligent/rfis-currently-available/ About The Avoca Group The Avoca Group, whose clients include top five pharmaceutical companies and global contract research organizations (CROs), is a driving force behind the continuous improvement of outsourced clinical research. In 2011, the Avoca Quality Consortium™, a pre-competitive collaborative, was formed and sponsored by Pfizer and Lilly. Members include more than 70 pharma, biotech, and clinical service providers. Founded in 1999, the company works exclusively in the health care industry with a focus on clinical research and clinical outsourcing. Learn more about The Avoca Group at www.theavocagroup.com and on LinkedIn and Twitter.
FDA Approves Nipocalimab for the Treatment of Generalized Myasthenia Gravis
April 30th 2025Approval is based on results from the pivotal Vivacity-MG3 trial in which IMAAVY (nipocalimab-aahu) demonstrated superior disease control throughout 24 weeks when compared to placebo plus standard of care.
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.