Ultra-Scan to Showcase Biometric Technology Established to Assist in Clinical Trial Management
Ultra-Scan's TouchLink Solution Allows CROs to Accurately Identify Patients and Ensure Study Integrity.
Buffalo, NY-June 13, 2006-As federal regulations become stricter, it is important for clinical research organizations (CROs) to take the necessary measurements and precautions to accurately identify study participants and their eligibility for clinical trial participation. Ultra-Scan Corporation, an identity management solutions provider, will showcase its TouchLink Identity Management Software at the Drug Information Association's 42nd Annual Meeting in Philadelphia. Researchers and trial administrators will have the opportunity learn more about this revolutionary technology in support of clinical trials.
Ultra-Scan's TouchLink Identity Management Software offers clinical research organizations an accurate and cost-effective solution for establishing, managing and repeatedly validating subject identity. TouchLink provides standalone or integrated identification utilizing Ultra-Scan's patented ultrasonic fingerprint identification system to quickly and easily enroll and identify a subject population within a single site or across multiple sites and facilities. From screening through post-study follow-up, TouchLink can positively impact study results and enhance subject safety by providing essential identity validation. In turn, this ensures that each authorized subject is properly tested, treated, monitored and reimbursed during clinic and study encounters.
TouchLink is supported by Ultra-Scan's patented Livescan Ultrasonic Identification Systems (LUIS™), a biometric technology that uses ultrasound, high frequency sound waves, to capture high quality fingerprint images across all user populations and operational environments. LUIS can "see through" dirt, newsprint, hand lotions and other common finger contaminants, guaranteeing unsurpassed accuracy, reliability and ease of use.
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.
