
EDG: Medical Writing Peer Review of Clinical Trial Documents
€100.00 ex VAT
7 in stock
Description
Medical writers are often required to critically review work produced by their colleagues. This review typically includes elements that depart from standard quality control checklists, with a greater focus on consistency, completeness, adherence to guidelines, and scientific rigor. During this Expert Discussion Group, we will examine the elements that contribute to a useful and constructive Peer review. The discussion will focus on clinical trial documents including, but not limited to, clinical trial protocols, clinical study reports, and informed consent forms.
