Development & Strategy Clinical Study Reports

Clinical Study Reports

CTI routinely prepares Clinical Study Reports (CSRs) as part of our work for our sponsors. We work closely with sponsors to ensure accurate data presentation and interpretation, strict adherence to regulatory guidelines, and sponsor requirements.  Our group of medical writers and research scientists will quickly analyze data and present it in a meaningful way, ensuring a high quality study report. We have an independent Quality Assurance team that ensures quality is the leading factor in all of our services and is reflected in all of our submissions to regulatory authorities. 

Stephanie Makepeace
Senior Scientist, Regulatory & Scientific Affairs
A graduate of CTI’s research associate program, Stephanie has a background as a perfusionist.  Her scientific foundation combined with her knowledge of ICH and technical abilities has made her a strong resource in writing and reviewing a wide array of regulatory documents.

Stephanie Makepeace

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