Protocol Development and Case Report Form (CRF) Design
FRS is experienced in working with your project team in developing the study protocol(s) and the associated CRF. We follow the ICH and ISO guidelines for protocol development and format.
Creating a protocol that meets the requirements of the domestic and international community and which also provide clear and understandable direction to the investigational sites requires a thorough understanding of the testing to be performed and the data to be collected to answer the clinical question.
FRS is skilled in creating CRF that, through layout and content, not only collect the appropriate study data but which also aid the investigational site in reducing effort and reducing transcription errors.
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