Technical Writing for the Regulated Industries 2019

Topics

• How the reporting process supports products in research, development, and the marketplace
• 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
• Assessing and writing to the audience to produce effective written correspondence
• How documents work in tandem from initial correspondence about a project to an approved protocol, amendments, and final study report
• Reviewing and revising documents
• How the active and passive voices work and how to choose the most appropriate one for the type of writing you are doing
• Writing patterns and knowing the answers to your questions about the English language

Who should Attend

• Quality Assurance Departments
• Research and Development Departments
• Manufacturing Departments
• Information Technology Departments
• Production Departments
• Operations Departments
• Anyone who wants an in-depth and comprehensive overview of the structure of the language and writing within the broad range of reporting that the industry requires
• Documentation Departments