Contact us to schedule a demo or for more information on our clinical trials software and outsourcing solutions
The ClinPlus Suite of clinical software products and outsourcing services offers solutions designed to enable your clinical study team to successfully manage and expedite clinical trials.
Our proven solutions are extremely flexible and allow Sponsors to define their unique standards and requirements for clinical studies and also allows 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 products support complex study designs and adaptive clinical trials as regulatory pressures force life sciences companies to design increasingly 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 data collection, coding, data analysis, safety and efficacy reporting and trial management to business process outsourcing, ClinPlus empowers clinical data management, biostatistics and clinical trial 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.
Our dedicated staff averages over 15 years experience in the clinical trials arena. We offer professional outsourcing services to help you maximize your clinical research software investment, gain early visibility to clinical data and assure your ongoing success.
Outsourcing Services include:
Every ClinPlus customer receives the highest level of support possible. Experienced professionals address issues in the same timely manner, whether you are a emerging, mid-size or large CRO, pharmaceutical, biotech or medical device company. We are proud to say that our support is among the best in the industry.