The Case Report Form (CRF) is a printed or electronic document designed to record all the clinical trial protocol required information on each trial subject.
The quality of the data collected relies first and foremost on the quality of the tool used to attain the data in a trial. Therefore, the design, development and quality assurance of such a tool must be given the utmost attention.
TechnoSTAT’s data management experienced personnel will help you make sure that your CRF is properly designed, is compliant with GCP guidelines and the study protocol and accommodate to the trial statistical requirements, while keeping the CRF as short and simple as possible for easy data entry. We believe that the more accessible the tool is, the more accurate the data is collected in it. Our team is well practiced and highly knowledgeable in CRF Design.
TechnoSTAT also offers CRF review, helping you avoid mistakes that will require extra work and can compromise your trial’s data validity.
We will work closely with your clinical team to help provide a valuable instrument for clinical data collection, to ensure easy data entry, better data validity and meaningful statistical analysis.