At CQ Advisory, we deliver comprehensive strategic and scientific expertise across the entire clinical research and development continuum. Serving as your dedicated in-house medical monitoring partner, we collaborate seamlessly with sponsor-designated CROs to optimize protocol development, streamline clinical operations, and ensure robust pharmacovigilance oversight. Our integrated service portfolio encompasses medical monitoring, health economics and outcomes research (HEOR), pharmacovigilance, medical writing, clinical data analysis and quality assurance - delivering trials that are operationally efficient, regulatory compliant, and strategically positioned for global market success.
End-to-end clinical trial support encompassing comprehensive clinical documentation development.
CRO partnership through strategic liaison coordination, systematic investigator and site selection processes.
Medical writing expertise spanning research documentation, peer-reviewed manuscripts, conference abstracts, and healthcare content development.
We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.