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Measuring SOP Effectiveness Across Training, Qualification, GMP Operations, and AI-assisted environments

Learn how to measure and improve SOP effectiveness across training, qualification, GMP operations, and AI-assisted environments — connecting documentation, compliance, and workforce performance.

4.8(0 reviews)
1.5 hoursThursday, July 23, 2026
Michael Esposito

Instructor

Michael Esposito

GMP Training & Document Management Specialist

What You'll Learn

Learn the parameters of an effective SOP
Define processes better by effective interaction with the SOP process owner and/or author
Integrate the SOP effectively into the position curricula of employees
Leverage the connection between SOPs and job performance
Employ various methods to measure retention of SOP content at the training stage
Use investigations and CAPAs to measure SOP effectiveness
Adapt existing effectiveness methods to AI-related changes

About This Event

Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical employees are required to perform. There are opportunities to leverage these procedures to measure and improve training effectiveness and job performance. In this course you will learn the vital connection between the documentation, compliance, and training spheres, how to maximize this connection to improve the quality of both SOPs and training, and adapt existing methods to the rapid changes brought about by AI. WHY YOU SHOULD ATTEND To learn the parameters of an effective SOP; 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 leverage the connection between SOPs and job performance; to employ various methods to measure retention of SOP content at the training stage; to use investigations and CAPAs to measure SOP effectiveness; and to adapt existing effectiveness methods to AI-related changes. Code: FDB1285

Curriculum

Deciding the Main Objectives of the SOP
10 min
Interacting with the SOP Process Owner/Author to Improve Writing
8 min
Using Process Excellence Tools to Create Robust Procedures
8 min
Communication Between Documentation and Training During SOP Development
7 min

Requirements

  • Working in pharmaceutical, biotech, or other regulated manufacturing environments
  • Applicable to quality, documentation, training, operations, and compliance professionals

Who Should Attend

Quality Departments, Production Departments, IT Departments, Documentation Control Leaders, Manufacturing Departments, Operations Departments, Regulatory Affairs Departments, R&D Departments, Compliance Departments, and Management — essentially everyone in the organization who is tasked with creating or reviewing procedures.

Areas Covered

Deciding the Main Objectives of the SOP
Interacting with the SOP Process Owner/Author to Improve Writing Quality
Using Process Excellence Tools to Create a Robust Process and Procedure
Communication Between Documentation and Training During SOP Development
What SOP Writers and Approvers Need to Keep in Mind for Retention
Translating the SOP into Effective Curriculum Development and Training Execution
How SOP Wording Can Be Adapted for Learner-Appropriate Delivery Formats
Performing Ongoing Assessment of Knowledge Retention for Continuous Improvement
Using Investigations and CAPAs to Measure SOP Effectiveness
AI and Its Impact on Production, Compliance, and SOP Effectiveness Methods

Meet Your Instructor

Michael Esposito

Michael Esposito

GMP Training & Document Management Specialist

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 areas including Packaging, 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.

30 Years Pharmaceutical IndustryPfizer & J&J AlumniGMP TEA MemberConsent Decree Expert
Quantity
1

Single Access

$240.00
Buy Now
Secure payment via Stripe
Certificate of completion

Event Details

Format

Live Webinar

Duration

1.5 hours

Certificate

Included

Date

Thursday, July 23, 2026

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