DZS Software Solutions to preview ClinPlus® Clinical Trial Management System (CTMS), ClinPlus Report, and ClinPlus Data Management Solution Suite at 45th Drug Information Association Annual Conference in San Diego, California June 21-24, 2009

ClinPlus® expands their existing suite of clinical trial software and service solutions to include web-based Clinical Trial Management System (CTMS)

 

 

 

 

 

 

 

 

Bound Brook, NJ (June 15, 2009) - DZS Software Solutions, Inc., developers of the ClinPlus brand of products, is a technology and services leader focused on global clinical trial solutions. DZS today announced they will be unveiling new branding as well as a new Clinical Trials Management System (CTMS) and a number of exciting new features and functionality to their existing ClinPlus Solutions Suite of products that include ClinPlus® Data Management and ClinPLus ®Coding.

Until recently, many research organizations have delayed the adoption of new CTMS technology due to the complexities of implementing such a system across their enterprise. Technological change of this scale that affects all areas of an organization requires new workflows and changes in inefficient, but well established manual routines can be extremely difficult and time-consuming to accomplish.

DZS‘s new web-based ClinPlus CTMS, based on Microsoft .NET technology makes the utilization and integration of information across the enterprise much easier than in the past. The ClinPlus CTMS dramatically improves site productivity by eliminating redundant systems and manual tasks and helps enforce adherence to trial procedures. The system also provides a real-time trial financial and recruitment picture with immediate access to data about patient recruitment and reimbursement. ClinPlus CTMS is designed to track the status of people, events, data and finances and documentation involved in and required for a clinical trial. It tracks planned activities and events to ensure that they occur, and notifies users about upcoming activities and events. The system allows research professionals to be proactive rather than reactive where possible, and enables the control and management of clinical trials in ways not possible when only spreadsheets or manual processes are used. The ClinPlus CTMS can proactively warn organizations of out-of-variance patient visits, deficient regulatory documents or documents due to expire, and unresolved monitoring issues. This capability enables resolution of queries within minutes rather than hours needed to find and possibly miss these issues. And because the system is web-based, all that's needed is an internet connection and a computer. As a hosted solution it offers low start-up costs, very few IT implementation issues, robust data security and unmatched levels of efficiency. And, by improving overall efficiency, ClinPlus CTMS helps reduce product timelines and meet trial deadlines.

DZS/ClinPlus will be exhibiting their suite of products at the San Diego Convention Center, Booths 1024-1026 from 9AM Monday June 22nd through 4:00PM Wednesday June 24th. Prospects are encouraged to arrange comprehensive system demonstrations by contacting: salesandmarketting@clinplus.com.

About 45th Annual DIA Meeting.

The DIA Annual Meeting is the biopharmaceutical industry's largest global, multidisciplinary event. The 45th DIA Annual Meeting's focus is 'Better Medicines: Improving Safety with Every Step' and is being held June 21-25, 2009 at the San Diego Convention Center in San Diego, California. For the first time ever, DIA is offering LIVE online content from the Annual Meeting. For more information on the meeting, visit http://www.diahome.org.

About DZS Software Solutions, Inc.

DZS Software Solutions, Inc. (www.clinplus.com) 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, 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 every system!

Contact:

Keith W. Ward

Director of Global Marketing

DZS Software Solutions, Inc.

1661 Route 22 West,

Bound Brook, NJ 08805-1258

Office: (732) 764-6969 Ext: 129

Fax: (732) 764-6755

kward@clinplus.com

www.clinplus.com