Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries 2016

Topics

• How the reporting process supports products in research, development, and the marketplace
• The 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 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
• How to organize and deliver information based on the message
• How to assess and write to the audience
• The innate structures of English grammar
• How to structure reports
• How the active and passive voices work and how to choose the most appropriate one for the type of writing you are doing
• How to create grammatically sound passages
• How to review and revise documents
• Have a working knowledge of punctuation marks and their role in making documents readable
• Have increased confidence in writing and revising documents
• [[ your ]] own writing patterns and know the answers to your questions about the English language

Who should Attend

Attendees from:

• Quality assurance (QA)
• Scientists, engineers, and technicians in research and development
• Manufacturing
• Information technology (IT)
• Administrative staff that must prepare documentation in support of R&D and operations activities
• Other operations professionals
• 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