The ClinPlus Suite of clinical trial software products and clinical outsourcing services offers solutions designed to enable your clinical study team to successfully manage and expedite clinical trials. 

Our solutions are proven  and extremely flexible and allow Sponsors to define their unique standards and requirements for clinical studies and also allow CROs to meet varying demands from multiple-study Sponsors while satisfying the strict guidance requirements of the FDA, EMEA and other regulatory authorities worldwide. 

Clinplus clinical data management, coding, report and trial management products 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 and our commitment to evolve as the clinical trials landscape changes.  

 From clinical data management that involves collection, coding, data analysis, safety and efficacy reporting and clinical trial management to business process outsourcing, ClinPlus empowers clinical data management, biostatistics and clinical trial management teams to increase their accuracy and efficiency when conducting mission critical tasks.

 DZS/ClinPlus clients also enjoy a low total-cost-of-ownership (TCO), second-to-none support and a peace-of-mind that comes with using our proven solutions.