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The CRA creates reports that have many audiences, one being regulatory authorities reviewing essential documentation for the review of clinical trials linked to marketing application approvals. This course presents 10 categories of scientific report writing in the context of the role of the CRA and the reports that they write. The applicable reports are monitoring visit reports, e-mails, telephone reports, memos to file, and more.  The concepts of writing in a scientific voice versus first person, objective versus subjective and many more are presented.  This course is invaluable for the CRA, as well as the individual who critiques the various reports.