DZS/ClinPlus® demonstrates enhanced functionality for ClinPlus CTMS® and ClinPlus Report®

DZS Software Solutions Inc. will unveil new functionality for their suite of clinical trial software products -Data Management, Coding, Report and Clinical Trial Management. Stop By Booth# 927

Bound Brook, NJ - June10, 2010 - DZS Software Solutions, Inc. plans on demonstrating several new enhancements for their clinical solutions at the upcoming DIA Annual Conference in Washington DC, June 13^th-16th.  (DZS is at Booth #927).

Since 1996, DZS Software Solutions Inc., innovators of the ClinPlus brand of products has been committed to providing the most technologically advanced clinical software products to manage the data of clinical trials, to life science professionals, helping them streamline the clinical trial process and accelerate the process of bringing life-enhancing medicines, biologics and devices to market.

Most recently, DZS responded to industry challenges to increase clinical trial productivity and reduce operating expense by launching a web-based clinical trial management system (CTMS) at last year's DIA Annual in San Diego. Since that time, the system has gained increasing acceptance because of its ability to improve site productivity, eliminate redundant systems and existing manual tasks and help enforce adherence to trial procedures and regulatory compliance. The system also helps provide a real-time trial financial and recruitment picture with immediate access to data about patient recruitment, site payments and supply inventory.

Several newly developed modules will be demonstrated at DIA, including online site visit trip report design and workflow tools (including electronic signatures), automated event notifications and subscriptions to scheduled reports.  An upcoming release planned for later this year will include these features, as well as other new capabilities such as SAE worksheet tracking, additional global reporting options, and enhanced subject visit schedules to handle multiple cohorts or cycles.

DZS/ClinPlus has also partnered with APT, an information technology firm located in Allentown, PA, to host ClinPlus(CTMS) and provide Software-as-a-Service subscription model pricing and accessibility for our global customers. The partnership with APT provides value-added technology services for all of the ClinPlus product line to meet the stringent needs of the pharmaceutical industry for 21CFR Part 11 compliance.

In response to the recent clinical data study standards set out by the Clinical Data Interchange Standards Consortium (CDISC), specifically with regards to the Study Data Tabulation Module (SDTM) and the Analysis Data Model (ADaM), DZS enhanced their SAS-based ClinPlus Report software so that adhering to and properly managing these data standards among workgroups, between departments and across the enterprise could be achieved much more efficiently, resulting in dramatic time and cost savings, increased productivity and earlier visibility to reliable clinical data. ClinPlus Report also touts an extensive template library (50+) for generation of CDISC/ ADaM compliant safety tables and listings for ten data domains with supporting documentation in a validated, standardized way.

According to Bob Borysko, VP of Programming and Development at DZS Software Solutions, "These developments underscore our commitment to helping the life science industry meet the challenges of both regulatory and standards-setting bodies as efficiently and effectively as possible." Added Mr. Borysko "Our goal is to offer robust solutions to help our clients leverage these standards and expedite their clinical trials."

To speak to a product expert or arrange a personalized demonstration, please contact sales&marketing@clinplus.com or follow this link to request specific information or pricing: http://www.clinplus.com/products/clinical-trial-management-software?utm_campaign=CTMS-1.1-Promo&utm_source=Fast%20Pitch%2C%20LinkedIn%20Groups

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, 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 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

http://www.linkedin.com/profile

kward@clinplus.com

http://www.clinplus.com/