We are excited to be releasing version 2.0 of this system. This release contains many enhancements, the highlights include a unique site visit report completion tool and review workflow , custom notifications, report scheduling/delivery and direct integration with Medidata Rave and other CDISC compliant EDC and IVRS systems. In fact, DZS has recently become a Medidata Technology Partner.
Initially released in November of 2009, ClinPlus CTMS is our youngest product in our 16 year history. With the recent introduction of version 2, this system is quickly gaining popularity with contract research organizations and sponsors in various sectors of drug, biotech and medical device development.
Our clients chose ClinPlus CTMS primarily for its clean, logical design. This ensures successful training and acceptance within the user population as they can concentrate on their tasks rather than struggle with an unwieldy system.
Steve Trigilio, the chief architect of ClinPlus CTMS, has more than 20 years clinical experience in various roles including CRA, Clinical Project Manager, Chief Technical Officer, and Systems Architect. This real-world experience is evident in this product as he is able to design from the user’s perspective, regardless of their role.
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. Our aggressive pricing structure is also helping to win clients. We offer the software as a purchase, lease or Software as a Service (SaaS) Universities and other not-for-profit organizations enjoy a 30% discount off our commercial pricing (not applicable for SaaS).
The Site Visit Report Completion Tool and Workflow
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.
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