Overview

This module reviews the publication planning process and walks through steps and considerations for developing publications. It also covers the role of a medical writer as well as the guidances that govern the creation of publications.

The module was written with clinical trial publications in mind, as they’re the most relevant for its Medical Affairs audience. However, some content is also applicable to scientific and pre-clinical publishing.

This module takes an average of 1.25 hours to complete.

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

Featured topics

Publication planning
Publication development
Role of scientific medical writers
Publication guidances

Who should attend?

This course is designed for professionals involved in:
- Medical Communications
- Medical Affairs
- Medical and Scientific Publication Planning and Development
- Scientific and Medical Writing
- Commercialization and Product Brand Planning

Learning objectives

At the conclusion of this course, participants should be able to:

List the components of a publication plan
Outline process steps and considerations for developing a publication
Recognize the role of a medical writer in the publication process and the differentiation from ghostwriters
Identify the role of various guidances that govern medical publications

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Publication Planning and Development

Overview

Featured topics

Who should attend?

Learning objectives

Be informed and stay engaged.