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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


    • 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


    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


    Michael Esposito has 30 years experience in the pharmaceutical industry and 13 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 organization GMP TEA 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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    On Demand

    Transcript

    PDF Transcript of the Training which are available once the webinar is completed.(Transcript for single user only)

    $179

    Downloadable recorded session

    Get unlimited access to the link for six months.

    $225

    Training CD

    Free shipment within 72 Hours, from the date of webinar completion.

    $350

      

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