2019 - Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries

Mandates for documentation set forth by the regulators, such as the Food and Drug Administration (FDA), the International Organization for Standardization (ISO), and other governing bodies
How the reporting process supports products in research, development, and the marketplace
How documents work in tandem from initial correspondence about a project to an approved protocol, amendments, and final study report
Assessing and writing to the audience to produce effective written correspondence
How the active and passive voices work and how to choose the most appropriate one for the type of writing you are doing
Reviewing and revising documents
Writing patterns and knowing the answers to your questions about the English language