At CQ Advisory, we help identify and address the gaps for your unique clinical development needs in order to provide complete coverage of your clinical trials.
Acting as in house medical monitor including EDC review, input and comments.
Reviewing and advising on clinical development plans, protocol design, investigator and site selections & conducing clinical coding reviews.
Abstract and manuscript write up, CIOMS, Investigator Brochure , clinical study report review and finalization.
Health economic outcome research (HEOR) studies.
Clinical literature search, analysis and presentation.
Clinical trials document drafting (i.e. CRF, CTA, SOP’s etc.).