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Best Practices of Writing SOPs - Webinar

  • ID: 4899673
  • Webinar
  • July 2019
  • Region: Global
  • 90 Minutes
  • Compliance Online
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Why Should You Attend:

Attend this webinar to improve the writing of both SOPs and training materials for more effective training and reduction of errors. Through this interactive course, learn how you can:

To learn the parameters of an effective SOP
To distinguish a well-written SOP from a poorly written one
To define processes better by effective interaction with the SOP process owner and/or author
To integrate the SOP effectively into the position curricula of employees
To explore the connection between SOPs and job performance, and measure retention of SOP content at the training stage
Areas Covered in the Webinar:

Regulatory requirements for SOPs - consequences for inadequate SOPs or failure to follow 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
Interact with the SOP process owner/author to improve the writing of procedures
Using process excellence tools to create a robust process and procedure
Basics of grammar and style
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
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Michael Esposito has over 30 years experience in the pharmaceutical industry and 17 years experience in GMP training and document management. He has worked for Wyeth Pharmaceuticals, Pfizer and Johnson & Johnson's McNeil Consumer Healthcare Division in a variety of areas including Packaging, project administration, Quality Assurance, Government Contracts, translations, systems training, and international operations. He collaborated in the development and implementation of the training portion of the Consent Decree workplan for McNeil and revised their introductory GMP course. He is a member of the training organizations GMP Training Educators Association and Association for GXP Excellence and is fully fluent in Spanish. His areas of interest include systems training, training effectiveness, post-training user support, process improvement, and sustainable packaging.
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