The ClinPlus Suite of clinical trial management software 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. They 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, MedDRA coding, WHO Drug coding, clinical programming and clinical trial management 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.  

 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 enables teams who use clinical trial management systems 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 the assurance that comes with using our proven solutions.