Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries 2016 covers topics such as:
- 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
Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries 2016 brings together 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