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Starting her career as a CRA, progressing to Project Manager and Medical Writer, Wendy Kingdom has experience of writing all study-related documents from Protocols Clinical Study Reports Information for Patients Leaflets and Consent Forms Other patient information such as instructions for using medication, and appointment cards Regulatory summary documents, including clinical summaries and overviews, PIPs, ODDs, clinical expert statements for product license renewals, and editing of scientific advice documents Ethics Committee applications Safety narratives SOPs Manuscripts for publication |