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 CRO for life science companies that are searching for a true partner. With over 30 years of experience in a wide range of therapeutic areas and pharmaceutical research support, we have the knowledge and the expertise to help your teams meet their goals in areas ranging from statistical programming to clinical trials, as well as all areas related to Data Management, Programming, Biostatistical Consulting, and Medical Writing.
We specialize in all aspects of clinical data management, including outsourcing, staffing and placement, statistical programming, scientific writing, and biostatistical consulting.
Whether you need traditional Clinical Data Management outsourcing, or a customized solution to meet your organizational needs, DZS has a solution that’s right for you.
- Clinical Data Management
- Drug and AE Coding
- CDISC Programming Services
- Statistical Programming
- 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.
Check out our Blog...