A Flexible Approach To Early Phase Clinical Trials

With eight Phase I sites on three continents, QPS offers comprehensive services from small-scale, complex and high-capacity studies in healthy volunteers, to Proof of Concept (POC) studies in patient or specialty populations for a wide variety of therapeutic indications.

Each Phase I study will have a client dedicated team, headed by an experienced Clinical Project Manager, who has the overall responsibility for the conduct of your study and is your single point of contact throughout your Phase I study. As a full service unit, QPS can assist you with the entire early phase drug development process:

• Review of Preclinical Data
• Study Design and Protocol Writing
• Clinical Conduct
• Provision of CDISC-compliant Clinical Study Reports
• Data Management
• PK/PD Analysis
• Biostatistics
• Bioanalysis Assays
• Biomarker Assays