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 1. Eventura World
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 3. 3-Hour Virtual Seminar on Bad Standard Operating Procedures (SOPs) – Bad
    Training: Garbage In, Garbage Out


3-HOUR VIRTUAL SEMINAR ON BAD STANDARD OPERATING PROCEDURES (SOPS) – BAD
TRAINING: GARBAGE IN, GARBAGE OUT

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🎤  Michael Esposito      |  📅  January 30, 2023   |  🕒  11 AM Eastern Time US



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Why You 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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DESCRIPTION:

Standard Operating Procedures (SOPs) are necessary to demonstrate compliance
with regulations and operational practices. It also serves as a documented
roadmap which ensures consistency. This is integral to a strong quality system.
If you want to improve SOPs writing and training materials that create more
effective training as well as help in the reduction of errors, this webinar is
for you.

 * Learn to define the parameters of an effective SOP
 * How your foundation keeps subsequent steps from going awry-preventing
   “garbage in”
 * What interactions are necessary with the SOP process owner/author to improve
   the writing of procedures
 * How can we translate the SOP into effective curriculum development and
   training execution
 * Considerations related to curricula and Learning Management Systems (LMSs) o
   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

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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





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FDA SOP Bad training Virtual Seminar
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