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Live WebinarNew

ChatGPT-Assisted Technical Writing

Learn practical, compliant approaches to using ChatGPT for SOP drafting, document development, and technical writing in regulated industries.

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1 hourWednesday, June 24, 2026
Charles H. Paul

Instructor

Charles H. Paul

President, CHP Consulting LLC — Regulatory Compliance & Operational Excellence

What You'll Learn

Develop effective prompts to produce structured, regulatory-compliant outputs
Use ChatGPT for SOP drafting, document development, and standardization
Convert unstructured notes and legacy content into formal documentation
Maintain accuracy, traceability, and authorship control over AI-generated content
Align AI-assisted writing with ALCOA+ data integrity principles
Integrate ChatGPT into existing documentation workflows without disrupting quality systems
Define governance: roles, responsibilities, and risk considerations for AI use

About This Event

Technical writing in regulated industries — particularly pharmaceuticals, biotechnology, and medical devices — requires precision, consistency, traceability, and compliance with strict regulatory expectations. Documents such as SOPs, clinical reports, validation protocols, and regulatory submissions must not only be accurate but also structured in a way that supports usability under real-world conditions. The emergence of tools like ChatGPT introduces a new opportunity to enhance technical writing processes. However, most organizations are still unclear on how to use these tools effectively — especially within regulated environments where data integrity, authorship, and validation concerns must be addressed. This webinar focuses on practical, controlled, and compliant approaches to using ChatGPT as a support tool in technical writing — not as a replacement for human expertise, but as an accelerator for structured, high-quality document development. Code: FDB3769

Curriculum

Role of AI in Technical Writing for Regulated Industries
8 min
Capabilities and Limitations of ChatGPT
8 min
Developing Effective Prompts for Structured Outputs
10 min

Requirements

  • Experience writing SOPs, validation documents, or technical reports
  • Working in pharmaceuticals, biotech, medical devices, or other regulated industries
  • Basic familiarity with ChatGPT or similar AI tools is helpful but not required

Who Should Attend

Technical Writers, Regulatory Affairs Professionals, Quality Assurance Specialists, Validation Engineers, Clinical Documentation Professionals, SOP Authors and Reviewers, Project Managers in Life Sciences, and Training and Documentation Managers.

Areas Covered

Role of AI in technical writing for regulated industries
Developing effective prompts for structured outputs
Using ChatGPT for SOP drafting and document development
Improving clarity, readability, and usability of technical documents
Maintaining accuracy and validating AI-generated content
Ensuring traceability and authorship control
Aligning AI use with ALCOA+ data integrity principles
Risk considerations and governance for AI-assisted writing

Meet Your Instructor

Charles H. Paul

Charles H. Paul

President, CHP Consulting LLC — Regulatory Compliance & Operational Excellence

Charles H. Paul is President of CHP Consulting LLC, a regulatory compliance, operational excellence, training, and technical documentation consulting firm supporting pharmaceutical, biotechnology, medical device, and advanced therapy organizations worldwide. With more than 30 years of experience in regulated manufacturing environments, Charles specializes in helping organizations build sustainable quality systems that support compliance, operational performance, workforce effectiveness, and inspection readiness. His experience includes GMP quality systems, manufacturing operations, technical training development, process validation, deviation management, CAPA systems, operational excellence, documentation systems, and regulatory inspection preparation. Charles has supported organizations implementing new technologies, expanding manufacturing operations, establishing quality infrastructures, and preparing for complex regulatory inspections. He is a recognized author, speaker, and consultant who has delivered numerous webinars and seminars on GMP compliance, quality systems, human performance improvement, technical documentation, inspection readiness, and operational excellence throughout the life sciences industry.

30+ Years Regulatory ConsultingAdvanced Therapy GMP SpecialistSOP & Documentation ExpertLife Sciences Trainer & Author
Quantity
1

Single Access

$190.00
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Certificate of completion

Event Details

Format

Live Webinar

Duration

1 hour

Certificate

Included

Date

Wednesday, June 24, 2026

Topics

ChatGPTTechnical WritingSOPsAI ToolsRegulatoryDocumentationALCOA+

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