Clinical Trials Software
ClinPlus Data Management
Capture electronic and paper-based data within a single data management system. Learn More...
Manage your trials with a web-based Clinical Trials Management System for Sponors and CROs. Learn More...
Code meds and adverse events using WHO Drug, MedDRA or any other dictionary. Learn more...
Convert CDISC SDTM to ADaM and produce all safety and efficacy tables and listings. Learn more...
Sales and Support:
1-866-254-6758 (toll free, US)
1-732-764-6969 (outside US)
DZS is a SAS software reseller. Let DZS save you money on your SAS licensing. Contact Bob at: 732-764-6969 Learn more...
Clinical Trials Services
DZS Clinical Services is the Contract Research Organization for Life Science Companies who are searching for a true partner. With over 30 years of experience in a wide range of therapeutic areas and levels of research support, we have the knowledge and the expertise to help your teams meet their clinical development goals. We combine a unique brand of flexibility from our services division with our proprietary ClinPlus software, all built on a foundation of quality. As a result, we have successfully provided tailor-made contract research and software services to some of the largest global pharmaceutical companies and the smallest biotech start-ups.
Whether you need to outsource an entire project to our team of experts, find talented individuals to manage your projects in-house, or require a customized Functional Service Provider (FSP) model to help execute your clinical program, you should expect the highest level of attention and quality from your outsourcing partners. As a quality-focused CRO, it’s our unique passion for clinical research and desire for excellence that differentiate us.
- Clinical Project Management
- Clinical Monitoring
- Clinical Data Management
- Medical Coding
- Statistical Programming and CDISC Implementation
- Biostatistical Consulting
- Medical Writting
- Customized FSP Models
- Staffing and Recruitment
DZS Software Solutions, Inc. developed the ClinPlus Suite of Software products to enable your clinical study team to successfully manage and expedite clinical trials. These products support:
Our solutions are proven and extremely flexible and allow Sponsors and CROs to define their unique standards and requirements for clinical studies while satisfying the strict guidance requirements of the FDA, EMEA and other regulatory authorities, worldwide.
ClinPlus systems support complex study designs and adaptive clinical trials as regulatory pressures force life sciences companies to design more complex and comprehensive studies. DZS's current software development roadmap demonstrates our focus on improving drug development, as well as our commitment to continually evolve as the clinical trials landscape changes.
DZS/ClinPlus clients also enjoy a low total-cost-of-ownership, second-to-none support, and the assurance that comes with using our proven solutions.
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