Bad Standard Operating Procedures (SOPs) – Bad Training: Garbage In, Garbage Out

MessageThis Webinar is over
Date Aug 14, 2018
Time (1:00 PM TO 2:00 PM)
Cost 16775.00
Online
Attend this webinar to improve the writing of both SOPs and training materials for more effective training and reduction of errors.
  • Define the parameters of an effective SOP
  • How your foundation keeps subsequent steps from going awry-preventing “garbage in”
  • Interact with the SOP process owner/author to improve the writing of procedures
  • Translate the SOP into effective curriculum development and training execution
    • Considerations related to curricula and Learning Management Systems (LMSs)
    • Considerations for training: reading of SOPs with assessments and/or classroom training
  • Perform an ongoing assessment of the knowledge retention of learners for continuous improvement
Areas Covered in the Session :
  • Regulatory requirements for SOPs
  • Define the parameters of an effective SOP – how your foundation keeps subsequent steps from going awry – preventing “garbage in”
    • Why bad procedures have a negative impact on training
    • What identifies a bad procedure
  • Identify appropriate level of detail for document
    • How the training department needs to be in the loop at the start of the SOP development process
    • What SOP writers and approvers need to keep in mind for retention of the content at the training stage
  • Translate the SOP into effective curriculum development and training execution
    • The implications of good training for successful SOP execution
    • How the SOP wording can be “translated” into language that is appropriate for learners if a presentation, computer-based training or classroom session is to be developed
  • Perform an ongoing assessment of the knowledge retention of learners for continuous improvement
    • Use several different methods
    • Take advantage of tools that already exist in your organization
  • Review of learning objectives

Who Should Attend:

This course will be of benefit to anyone who is an owner of a process, responsible for writing or reviewing procedures, and/or managing training in a GMP environment.
  • Pharmaceutical industry- particularly those areas that develop SOPs for the manufacturing or quality monitoring of pharmaceutical products, which would also include Information Technology (IT) employees who manage systems training
  • Quality Departments
  • Production Departments
  • Compliance Departments
  • Engineering Departments
  • R & D Departments
  • Management – essentially everyone in the organization who is tasked with creating or reviewing procedures

 


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