QPS Clinical Operations supports drug development in every clinical stage with a strong focus on Phase II-IV clinical trials and medical device studies. QPS Clinical Operations offices are located in the USA. Austria, Croatia, Czech Republic, Germany, India, Netherlands, Spain, and Taiwan. We conduct and manage clinical studies in accordance with International Conference on Harmonization-Good Clinical Practice (ICH-GCP) standards and all applicable regulatory requirements to pharmaceutical and scientific clients.
QPS has added a new capability, building clinical trial kits. We offer individualized service, fast turnaround times, and can ship to any global clinical trial site. Contact Us (link to contact form) for more information.
Data management for successful clinical trials. Data management is a fundamental element of a successful trial. This step is critical to your success.
High-quality medical writing is important to the regulatory success of our clients. Our medical writing writers have the therapeutic expertise necessary to deliver high-quality written material.
At QPS, we have systems in place to enable the identification, recording, reporting and analysis of safety information so that any safety signals that arise during a trial are quickly identified and acted upon.
Proven success in clinical trial project management. QPS will meticulously manage your late phase II-IV clinical research from start to finish.
Effective clinical trial site monitoring and management. Proper site management is an essential element of clinical trial execution and in ensuring trial success.
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