With over 30 years of experience in eClinical technologies, DZS Clinical Services can support your clinical research needs at all levels.
From electronic data capture (EDC) to interactive web response systems (IWRS) and clinical trial management systems (CTMS), we can help your site navigate the complex waters of eClinical technologies. Whether you are looking for management of monitoring activities, coding, analytics, or risk-based monitoring, we likely have an experienced solution that is right for you.
Drawing on over three decades of experience in a variety of platforms, our eClinical technology team is prepared to offer customized support options that provide the highest levels of security and functionality, all while maintaining ease of use.
Here at DZS, we understand the difficulties sponsors face in conforming to complex regulations that may span the globe. For this reason, all platforms deployed by DZS must pass through our extensive Quality Management System to ensure compliance with 21 CFR Part 11 and EU Annex 11.
With a team of over 400 clinical research professionals spanning three continents, you can rest assured that the DZS staff can satisfy the exacting standards of the Food and Drug Administration (FDA) and the European Medicines Agency (EMA), as well as other regulatory authorities worldwide.