Bound Brook, NJ (PRWEB) June 14, 2011
DZS Software Solutions, Inc., (http://www.clinplus.com - the makers of ClinPlus® brand clinical software), an innovative software solution that has served the Life Science market since 1992, will be offering live demonstrations of the new version of their ClinPlus CTMS 2.0 software at the Drug Information Association's 47th Annual Meeting, DIA 2011, to be held in Chicago on June 19-23, 2011. Booth # 1542-44
ClinPlus CTMS 2.0 is a next-generation web-based trial management solution which makes it easier to track, measure and report on virtually every aspect of a clinical trial or study program. The relational database at the heart of the CTMS displays clinical trial operations information at various levels including, among others, trial, country, site, investigator, product, clinical research associate (CRA) etc. The main interface to the ClinPlus CTMS provides a clean and logical representation of the trial activities including site activity, subject enrollment, clinical supplies inventory, communication logs, finances and system administration. In addition to an intuitive overall Project Overview, ClinPlus CTMS provides easy access to milestone events, top site enrollers, as well as other clinical trial related activities. Color-coded progress bars give immediate feedback and warnings if necessary to study stakeholders. Most screens present summary information first, and allow the user to drill down for more detail. Access to projects, sites, menus and features is restricted using role-based security. The “My Favorites” feature allows users to add shortcuts to their most frequently used screens onto the menu bar.
An all new Site Visit Report Tool feature enables CRAs and Project Managers to author and review trip reports, while managing the workflow from first draft through final approval. This new feature will enable clients to configure report templates based on visit type and country, and to integrate CTMS data directly into the trip report. Unlike many other trip report authoring tools, the data entered by the CRA while creating the report is deeply integrated with the main features of the CTMS to reduce data redundancy. Updates to system data elements commonly found in the trip report sections such as regulatory documents, issues, enrollment, SAEs and deviations are done while creating the report and do not need to be re-entered into other areas of the system.
The availability of ClinPlus CTMS in a SaaS delivery model is another extremely important and timely development for many emerging Life Science organizations struggling with the challenges of improving clinical trial productivity while at the same time reducing expenses.
"The appeal of our new SaaS delivery model is its immediate availability to Life Science organizations of all sizes, and its ability to accommodate a wide range of the requirements needed to quickly and effectively deploy the software and get clinical studies up and running in weeks and not months,” said Bob Borysko, DZS’s VP of Product Development. “By improving global user accessibility and communications, tremendous efficiencies and time savings can be realized, manual operations can be reduced and redundant data and tasks can be completely eliminated.”
Be sure to visit DZS at Booth # 1542-44 to arrange a demonstration, or contact salesandmarketing(at)clinplus(dot)com or visit http://www.clinplus.com/ctms-landing---clinplus-clinical-trial-management-copy
About DZS Software Solutions, Inc.
DZS Software Solutions, Inc. is a privately held company founded in 1996 providing clinical trials software for clinical data management and analysis to the biotech and pharmaceutical industry worldwide. Over 50 clients globally presently use ClinPlus® software for data collection and capture, data cleansing, coding, analysis, clinical trial management and reporting. When the software is coupled with DZS services and training, many ClinPlus clients have dramatically improved productivity and maximized the value of clinical research investments and gained a competitive advantage to get medicines and products to market faster.
The ClinPlus® Software Solutions Suite for Clinical Trials provides premium tools required by pharmaceutical companies, contract research organizations (CROs), biotechs, and medical device manufacturers to expedite clinical trials and meet the strict data formatting requirements of the FDA and other global regulatory agencies.
The ClinPlus® Software Solutions Suite’s unmatched cost-of-entry, scalability, flexible delivery options and exceptional training and support have gained DZS a reputation for delivering exacting quality and helping clients achieve early visibility to reliable clinical data. DZS software engineers possess decades of statistical analysis, clinical data management, clinical project management, and ADE/Drug coding and table/list/report building experience. This real-world experience is incorporated into every ClinPlus® system design and is evident in the reliability and enhanced features found in every system!
Keith W. Ward
Director of Global Marketing & Sales
DZS Software Solutions, Inc.
1661 Route 22 West,
Bound Brook, NJ 08805-1258
Office: (732) 764-6969 Ext: 129
Fax: (732) 764-6755
# # #