Our Clinical Development Team combines scientific expertise, open communication, and trust to build lasting relationships with our clients. We offer collaborative solutions throughout the entire clinical development process to provide you with high enrollment rates, industry-best timelines, high-quality data, and a competitive price.
QPS is ready to excel at any clinical trial operations project, whether it is a clinical trial we are leading as the only site, for clinical trials that we are participating in as one of many sites, or as a standalone service. We offer study design, project management, clinical trial site monitoring and management, data management, image analysis, statistics and statistical programming, medical writing, quality control, quality assurance, regulatory documentation, and data interpretation.
QPS’s custom-built research offers everything from à la carte services to full-service early phase clinical trial support packages. These services include, but are not limited to, proof of concept, first in man (SAD, MAD, FE, and gender), phase I, phase II, microdosing, imaging, pharmacokinetics, pharmacodynamics, human mass balance, bioavailability, bioequivalence, drug-drug interactions, and 505(b)(2).
At QPS, we pride ourselves in being a leading provider of late phase clinical trials. As a full-service CRO offering custom-built research services, QPS supports clients across the entire drug development continuum, all the way to NDA submission. With a professional and experienced staff, strict adherence to timelines, dedicated customer focus, preferred provider relationships, and a large network of investigators across a broad set of therapeutic areas, QPS is ideally suited to support your next clinical trial.