DZS Software Solutions to Preview ClinPlus® Clinical Trial Management System (CTMS), ClinPlus Report, and ClinPlus Data Management Solution Suite at 45th Drug Information
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 --(PR.com)-- 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.
###
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.
###
Contact
DZS Software Solutions
Keith Ward
732-764-6969
www.clinplus.com
Bob Borysko, VP Programming and Development
x128
Contact
Keith Ward
732-764-6969
www.clinplus.com
Bob Borysko, VP Programming and Development
x128
Categories