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.
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.
Improving Engagement While Maintaining Data Integrity & Validity
March 19th 2024In recognition of Women's Health Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and uMotif's Chief Product Officer, Julia Lakeland, discuss new technologies improving patient engagement and reducing the emotional and logistical burdens of participation, ethical considerations that should be addressed when implementing those technologies, while ensuring patient privacy, and much more.
Using Patient Reported Outcomes in Dermatology Trials
April 25th 2024In part 3 of this video interview with ACT editor Andy Studna, Melissa Mooney, director, eCOA sales engineering, IQVIA sheds light on the unique challenges of dermatology trials and how clinical outcome assessments can be implemented in them.