Quanticate
, a leading global provider of data-related clinical services recently announced its partnership with Clinical Ink, a US-based company that offers a tablet-based system for collecting electronic source data in clinical trials. The objective of the partnership is to provide a consolidated eSource solution to increase the quality of the data captured and to introduce real-time remote monitoring of data. Quanticate will be utilizing Clinical Ink’s award-winning SureSource® solution that has been proven to speed up the availability of clinical data from clinical research sites.
“As a Clinical Research Organization (CRO) specializing in data-related services, we have been actively working with our customers to develop solutions that can help to provide efficiencies, whilst improving overall quality,” explains David Underwood, Chief Executive Officer at Quanticate. “Our newly launched centralized service provision (CSP) approach is focused on centralizing data to gain additional insight and provide fast access to data within a study and across a portfolio. Our CliQ portal has been developed to offer this insight, and with the use of SureSource by Clinical Ink, access and visualisation of study data will be much quicker also.”
“We are pleased to partner with Quanticate to bring the benefits of eSource to the European clinical trial market,” commented Ed Seguine, CEO of Clinical Ink. “The benefits of our approach to eSource are immediately apparent and, when coupled with Quanticate’s additional services, will provide our customers with real opportunities to simultaneously reduce cost and increase quality in their clinical trial projects.”
In addition to offering traditional EDC and paper options, Quanticate plans to support SureSource as part of an integrated approach to replace EDC with technology that captures source data during a patient visit – no secondary data entry by sites and no source data verification by monitors. Clinical Ink’s SureSource platform has recently been recognized by Gartner Research, Microsoft, and the Society for Clinical Data Management for the “significantly disruptive potential in the area of EDC” that this eSource model represents.
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.
Reaching Diverse Patient Populations With Personalized Treatment Methods
January 20th 2025Daejin Abidoye, head of solid tumors, oncology development, AbbVie, discusses a number of topics around diversity in clinical research including industry’s greatest challenges in reaching diverse patient populations, personalized treatment methods, recruitment strategies, and more.
VERITAC-2 Trial Shows Vepdegestrant Significantly Improves Survival in ESR1-Mutant Breast Cancer
March 24th 2025Phase III VERITAC-2 trial results show vepdegestrant significantly improved progression-free survivalcompared to fulvestrant in patients with ESR1-mutant (ESR1m) advanced or metastatic breast cancer, but did not achieve statistical significance in the overall intent-to-treat population.