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The ClinPlus 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.

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DZS to Preview New EDC and CTMS Products at SCDM 2011

  
  
  
  

Clinical Trial Technology Leader to Preview New Web-based EDC and CTMS Product CapabilitiesSCDM 2011

Bound Brook, NJ, September 1, 2011 – DZS Software Solutions, Inc., a leading provider of ClinPlus® clinical trial software and service solutions (www.clinplus.com), today announced its plans for the Annual Meeting of the Society for Clinical Data Management (SCDM), taking place September 11-14 in Baltimore, Maryland. The SCDM Annual Conference is the world's largest education event for clinical data managers and related professionals, attracting approximately 650 attendees from across North America and around the world.

DZS will spotlight several major new product releases for their data management, electronic data capture (EDC), coding and clinical trial management systems (CTMS) which broaden their already existing trial software capabilities in capture, management and reporting of clinical, operational and safety data.

ClinPlus EDC® is an all inclusive, ASP .NET system that represents a three year effort by DZS to deliver a more flexible, lower cost alternative solution to larger EDC systems. ClinPlus CTMS 2.0 offers pharmaceutical, biotech and medical device sponsors and contract research organizations (CROs) simplified delivery under a new SaaS subscription model in addition to traditional installed and 3rd party hosted delivery options. ClinPlus CTMS 2.0 offers enhanced functionality with site visit report authoring and review workflow, automated email notification of events and alerts, scheduled report execution with email delivery, enhanced EDC integration and improved data importing capabilities.   

These new product releases reflect DZS’s ongoing focus on improving clinical trial productivity and leveraging new web-based technologies that increase the value of trial data and improve the quality of that data to support regulatory approval for new compounds, biologics and medical devices. DZS/ClinPlus will host booth demos (Booth #317) to showcase the capabilities and interoperability between these latest clinical technologies.

 

For more information, please email: salesandmarketing@clinplus.com or visit http://www.clinplus.com

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.

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