ChatGPT-Assisted Technical Writing
Learn practical, compliant approaches to using ChatGPT for SOP drafting, document development, and technical writing in regulated industries.
Instructor
Charles H. Paul
President, CHP Consulting LLC — Regulatory Compliance & Operational Excellence
What You'll Learn
About the event
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
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
Meet Your Instructor
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.
Event Details
Format
Recorded Webinar
Duration
1 hour
Certificate
Included
Access
Lifetime
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