DZS to Launch Upgraded eClinical Software at DIA
Bound Brook, N.J. - DZS Clinical Services, a global provider of clinical development and data analytic services, has announced that it will be launching its enhanced ClinPlus 3.1 eClinical software at the Drug Information Association (DIA) Annual Meeting in Philadelphia. The ClinPlus eClinical Platform combines electronic data capture, a clinical trial management system, an interactive web response system and eTMF functionality into a single, user-friendly platform. The eClinical software maximizes productivity while minimizing the risk in clinical programs by centrally managing system and project security, global contacts and institutions, project design reports and notifications. “The enhanced ClinPlus eClinical software will really be a differentiator. Through ClinPlus, coupled with our full-service clinical development strategy, we provide a direct line to improved clinical trial performance for our clients,”said Greg Ambra, vice president of clinical operations at DZS Clinical Services. “Having EDC, CTMS, IWRS and eTMF functionality unified under one proprietary software platform provides maximum flexibility, functionality and efficiency for our clients.” The software has a simplified role-based user interface that requires just a single sign-in to access all eClinical components. The advanced software platform also replaces EDC and CTMS integrations with simple mapping and seamless web APIs when users need to integrate with third-party systems. “We look forward to providing in-booth demonstrations of the newly enhanced software at DIA,” said Bob Borysko, vice president of programming and development at DZS Software Solutions, the parent company of DZS Clinical Services. To meet with the DZS team at DIA 2016, visit Booth 2009 or schedule an appointment. For more information about DZS Clinical Services’ capabilities, visit DZS.com. About DZS Clinical Services DZS Clinical Services provides clinical development and data analytic services for global pharmaceutical, biotech and medical device companies. DZS delivers improved clinical trial performance through clinical project and data management, clinical monitoring, medical writing, staffing and recruitment. DZS leverages its proprietary eClinical software platform ClinPlus® to help clinical study teams successfully and efficiently manage the collection of clinical data. Visit DZS.com to learn more about extending your clinical capabilities.
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.
