Mission Statement
Our mission is to serve the Life Science Industry with the highest level of integrity by providing software solutions and services aimed at improving the clinical trial process while reducing total operating expenses. Our mission is fulfilled through the mutual satisfaction of the needs of our clients, investors, and employees.
DZS ClinPlus has your solutions for clinical software and clinical services. Their mission is to serve the Life Science Industry with the highest level of integrity by providing software solutions and services aimed at improving the clinical trial process while reducing total operating expenses. They fulfill their mission through the mutual satisfaction of the needs of their clients, investors, and employees. Their clinical data management products have been helping clients in the pharmaceutical, biotechnology, medical device and contract research industries for more than fifteen years to manage clinical studies across multiple therapeutic areas and collect quality data so that they meet strict timelines and stay within budget.
The Clinical Trials Management System (CTMS) provides users with the flexible tools they need to easily configure their system so that it can meet their specific needs. ClinPlus offers a system that is both flexible and scalable. The web-based .NET software solution will empower your pharmaceutical, biotechnology or device organization and contract research organization to manage and collaborate on clinical trial operations so that clinical trial design is expedited and the set-up runs more efficiently. The benefit to you is a secure, stable, and centralized access to multiple sites, trials, and programs.
The Clinical Trials Management System can be conveniently used as web-based with most internet browsers. This allows you to efficiently collect and manage patient and trial administration data with enhanced data importing capabilities. You can use CTMS installed, as 3rd party hosted, or in a SaaS delivery model. Incorporating CTMS for your clinical data management will help you drastically reduce your trial administration costs while easily managing the investigator/patient process with a unique site visit report completion tool and review workflow. This mission of ClinPlus is evident in the features they offer in this product that help you perform clinical trials more easily while reducing your operating cost!
CTMS allows you to remain 21 CFR Part 11-compliant with the FDA, so that your organization’s integrity is intact. You will be able to track the site and overall aggregate study progress with user-defined indicators and graphically present enrollment metrics and projections and ensure immediate response. Save time when you monitor, schedule, sign and submit trip reports electronically. If you need custom reports to meet your specific client or business needs, the experts at DZS can configure them to meet your needs. The process will be simpler from start to finish when you store and search data on all personnel and stakeholders associated with the clinical study.
Go to www.clinplus.com to learn more about the Clinical Trials Management System that will simplify the clinical trials process at your organization. You will enjoy all of these convenient features in addition to a lower operating cost. With more than fifteen years of experience to back their products, DZS/ClinPlus has the expertise to provide you with the clinical software solutions that you can rely on. You can request a demo or ask them a question online or call 1866-ClinPlus to find out more. ClinPlus is your path to clinical trial success and they are waiting to show you the way!
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