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Enhancing the Clinicall Professional's Knowledge of Regulatory Documents

Title
Enhancing the Clinicall Professional's Knowledge of Regulatory Documents

Abstract
The author, an experienced freelance regulatory writer for the pharmaceutical industry, describes her experience contributing to the redesign and teaching of a distance learning graduate course titled Medical Writing for Clinical Research at George Washington University (Washington, DC). This course analyzes and evaluates major clinical research-related regulatory documents that contribute to product development.