Effective GxP Instructions Writing

The webinar discusses regulatory requirements for procedures, highlights errors in black and white text, and offers strategies for creating clear, concise, visual procedures with real-world examples.
  • Wednesday
  • October
  • 15
  • 2025
10:00 AM PDT | 01:00 PM EDT
Duration: 60 Minutes
IMG Matt Peplowski
Webinar Id: 61471
Live
Session
$119.00
Single Attendee
$249.00
Group Attendees
Recorded
Session
$159.00
Single Attendee
$359.00
Group Attendees
Combo
Live+Recorded
$249.00
Single Attendee
$549.00
Group Attendees

Overview:

The webinar provides a brief overview of regulatory requirements for procedures, and explains why black and white text procedures leads to more errors for end users. It also discusses benefits of and strategies for writing clear, concise, visual procedures for end users at a high level, with real-world examples.

Why you should Attend:

Companies spend major time and money writing SOPs, and training employees on SOPs, but little or no time or money training employees how to write SOPs. Yet SOPs are the cornerstone of all GXP operations.

This webinar changes the mindsets of document authors, reviewers, and approvers, and highlights the power of concise, visual information. We look at document writing through the lens of error prevention, and seek to eliminate the ‘old school’ mentality that SOPs have to consist primarily of black and white text.

The course benefits all employees in any industry who write, revise, edit, have input to, review, approve, and/or follow written instructions.

Areas Covered in the Session:

  • Regulatory requirements
  • What makes procedures hard to follow
  • The power of visual information
  • Do’s and Don’ts
  • Examples

Who Will Benefit:

  • Manufacturing Technicians, Operators, Associates, Leads, Supervisors, Managers, Associate Directors, Directors, Investigators, Compliance
  • Quality Control Analytical and Microbiology Technicians, Analysts, Scientists, Leads, Supervisors, Lab Coordinators, Managers, Associate Directors, Directors
  • QA and Quality Systems compliance, Specialists, Engineers, Validation, Supervisors, Managers, Associate Directors, Directors, Officers, Auditors
  • Engineering/Facilities/Maintenance - Engineers, Technicians, Leads, Supervisors, Managers, Associate Directors, Directors.
  • Supply Chain/Logistics/Warehouse - Material handlers, Shippers, Order Pickers, Inspectors, Supervisors, Managers, Associates, Leads, Directors
  • Manufacturing Science & Technology / Process Development - Scientists, Senior Scientists, Associates, Technicians, etc.
  • All Operations Personnel
  • Training and/or Learning & Development Associates, Coordinators, Supervisors, Managers, Instructional Designers
  • Project Managers, Program Managers
  • Planning Employees
  • Buyers

Speaker Profile

Matt Peplowski The goal of all of Matt’s training is to transform behavior and improve performance. Matt has over 30 years of experience in GMP Manufacturing, Quality, and Learning & Development. He is currently founder, owner, and president of BioPharm Error Prevention Associates, Inc.

He is an expert in SOP Writing, Human Error Prevention, cGMP, Quality Systems, and Learning & Development, and has designed and delivered highly engaging, effective, and interactive training, documentation, toolkits, and improvement programs extensively in these areas for many years.

He is a member of ATD and PDA, a former instructor for Massachusetts Biotechnology Council, and a current instructor for CfPIE, and the International Pharmaceutical Academy.