Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries

This technical writing training program will highlight the mandates for documentation set forth by the regulators, such as the FDA, the 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

For More Details:
https://www.complianceonline.com/tech...