Overview

This module familiarizes medical affairs professionals with the preparation of written responses to specific drug information questions.

The module takes an average of 1.75 hours to complete.

This eLearning module can be purchased individually or as part of the Medical Communications eLearning Program (eight modules) or the Medical Affairs eLearning Program (11 modules).

Featured topics

- Regulatory guidelines
- Writing tips and recommendations
- Anatomy of a standard medical letter
- Quality assurance - editing/review process

Upon completion of this module, learners should be able to:
- Recognize regulatory guidelines that govern industry-generated responses for medical information when writing standard medical letters
- Determine medical writing excellence in standard medical letters by verifying the use of data, scientific rigor, correct grammar, brevity, and/or clarity
- Identify the components of a complete standard medical letter
- Differentiate various levels of quality review that may be necessary for standard medical letters

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