Crf designing : challenging step in clinical data management

According to ICH guidelines for GCP, CRF can be defined as a printed, optical or electronic document designed to record all of the protocol required information to be reported to the sponsor on each trial subject. CRF development is one of the most crucial steps in Clinical trials as it preserve and maintains quality and integrity of data. CRF design should be standardized to address the needs of all users such as investigator, site coordinator, study monitor, data entry personnel, medical coder and biostatistician.
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