Reasons To Attend:
You should attend this course because it addresses how to write effective correspondence and reports in support of your company's activities. You will learn how to organize and deliver information for the intended audience. You will learn how to write clear and readable documents, and how to revise and refine your own and others' writing. The course provides an overview of sound grammatical conventions, addresses problematic areas of the English language, and affords opportunities to address specific language issues.
Areas Covered:
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
Learning Objectives:
Upon completion of this course, you will:
Understand 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
Know how the reporting process supports products in research, development, and the marketplace
Understand how documents work in tandem from initial correspondence about a project to an approved protocol, amendments, and final study report
Know how to produce effective written correspondence.
Scheduled on April 07 2021 1:00PM EDT