• Home
  • Writing and Enforcing Effective Standard Operating Procedures (SOP)

Writing and Enforcing Effective Standard Operating Procedures (SOP)

This course addresses how to write effective SOPs, and work instructions in support of your company's activities.Learning ObjectivesFood and Drug Administration (FDA), the International Organization for Standardization (ISO) requirements for documentationEffective written SOPs and work instructionsMandates for documentation set forth by the regulators, such as the Food and Drug Administration (FDA), the International Organization for Standardization (ISO), and other governing bodiesAssessing and writing to the audience to produce effective written SOPs and work instructionsHow the active and passive voices work and how to choose the most appropriate one for the type of writing you are doingReviewing and revising documents Writing patterns and knowing the answers to your questions about the English languageWho Should AttendQA and QC ManagersQuality EngineersValidation ManagersValidation Engineers and SpecialistOperations ManagersRegulatory Compliance Managers and PersonnelAnalystsTechnical WritersWhy Should You AttendYou will learn how to organize and deliver information for the intended audience. You will learn how to write clear and readable SOPs and Work Instructions, 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, and specific audiences. You will also learn how to implement good documentation practices within your SOPs.

This course addresses how to write effective SOPs, and work instructions in support of your company's activities.

Learning Objectives

  • Food and Drug Administration (FDA), the International Organization for Standardization (ISO) requirements for documentation
  • Effective written SOPs and work instructions
  • 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 SOPs and work instructions
  • 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

Who Should Attend

  • QA and QC Managers
  • Quality Engineers
  • Validation Managers
  • Validation Engineers and Specialist
  • Operations Managers
  • Regulatory Compliance Managers and Personnel
  • Analysts
  • Technical Writers

Why Should You Attend

You will learn how to organize and deliver information for the intended audience. You will learn how to write clear and readable SOPs and Work Instructions, 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, and specific audiences. You will also learn how to implement good documentation practices within your SOPs.