SOP Writing, Training and Compliance in the Pharmaceutical Industry

SOP Writing, Training and Compliance in the Pharmaceutical Industry is a conference that covers topics such as:

  • Define the parameters of an effective SOP
    • How your foundation keeps subsequent steps from going awry
  • Regulatory requirements for SOPs
    • What commitments you make when you put your process in writing
    • Using process excellence tools to create a robust process and procedure
    • Consequences of noncompliance
    • Keeping training in mind while writing procedures
  • Interact with the SOP process owner/author to improve the writing of procedures
  • Why poorly written procedures have a negative impact on production
    • Compliance risks with ambiguity or excessive detail
    • What identifies a poorly written procedure
    • Avoiding pitfalls in revising SOPs
  • Retention of the content at the training stage
    • Perform an ongoing assessment of knowledge retention of SOPs for continuous improveme
    • The implications of good training for successful SOP execution
  • Integrate the SOP effectively into the position curricula of employees
    • Why the training department needs to be in the loop at the start of the SOP development process
    • Relationship between SOPs and employees` training curricula
    • Relationship between SOPs, curricula and qualification to perform tasks

SOP Writing, Training and Compliance in the Pharmaceutical Industry brings together attendees who are owners of a process, responsible for writing or reviewing procedures, and/or managing training in a GMP environment from pharmaceutical companies.


Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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