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AI for CAPA and Investigations: Where It Helps and Where It Can Get You in Trouble

Learn where AI genuinely helps CAPA and investigations — and where it creates regulatory risk by replacing evidence-based analysis with generated logic.

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1 hourMonday, July 13, 2026
Charles H. Paul

Instructor

Charles H. Paul

President, CHP Consulting LLC — Regulatory Compliance & Operational Excellence

What You'll Learn

Understand regulatory expectations for CAPA and investigation quality and defensibility
Identify acceptable vs. high-risk AI use cases within investigation workflows
Recognize how AI can generate plausible but incorrect root cause determinations
Understand bias and limitations introduced by prompt structure and incomplete data
Learn how to maintain evidence-based conclusions when using AI-generated content
Apply human oversight and accountability requirements to AI-assisted investigations
Establish verification and review standards for AI-generated investigation outputs
Integrate a practical AI control framework into existing CAPA procedures

About This Event

Corrective and Preventive Action (CAPA) systems and investigation processes are among the most scrutinized elements of any quality system. These processes require structured problem-solving, objective evaluation of evidence, and defensible conclusions that can withstand regulatory review. With the introduction of AI tools such as ChatGPT, organizations are beginning to use automation to summarize data, draft investigation reports, and even suggest potential root causes. While this can improve efficiency, it introduces a fundamental risk: the substitution of generated logic for evidence-based analysis. Regulatory bodies, including the U.S. Food and Drug Administration, expect investigations to demonstrate clear linkage between observed events, supporting evidence, root cause determination, and corrective actions. AI-generated outputs, if not properly controlled, can weaken this linkage and create conclusions that appear logical but are not supported by data. This webinar addresses how to incorporate AI into CAPA and investigation workflows without compromising the integrity, depth, and defensibility of the process. WHY YOU SHOULD ATTEND Organizations are increasingly using AI to "assist" with investigations—but most are doing so without defined controls or clear understanding of the risks. AI can generate plausible but incorrect root causes, oversimplify complex multi-factor issues, miss critical contributing factors, and introduce bias based on prompt structure. These risks are not obvious on the surface. In many cases, the output looks structured and professional, which creates a false sense of confidence. From a regulatory standpoint, this is a major concern. Investigations must be evidence-based, thorough and complete, logically structured and defensible, and clearly attributable to qualified personnel. This webinar provides a structured approach to using AI as a support tool—without allowing it to replace critical thinking, analysis, or accountability. TOPIC BACKGROUND This webinar delivers a practical framework for integrating AI into CAPA and investigation processes while maintaining full control over analysis, decision-making, and regulatory compliance. The session begins by reviewing the core expectations for investigations within regulated environments, including the need for objective evidence, structured analysis, and defensible conclusions. Participants will examine how AI-generated outputs align—or conflict—with these expectations. The webinar then explores specific use cases where AI can provide value, such as organizing investigation data, structuring reports, summarizing large data sets, and improving documentation clarity. These applications are contrasted with higher-risk uses, particularly those involving root cause identification, causal reasoning, and corrective action determination. A key focus is understanding how AI can unintentionally introduce bias or unsupported conclusions. Participants will learn how prompt structure, incomplete data input, and over-reliance on generated outputs can lead to flawed investigations. The session emphasizes maintaining human ownership of the investigation process. This includes defining clear roles for reviewers, establishing standards for verifying AI-generated content, and ensuring that all conclusions are grounded in documented evidence. Participants will also learn how to integrate AI into existing CAPA workflows without disrupting established quality system requirements. The webinar concludes with a practical control model that organizations can implement immediately, ensuring that AI enhances efficiency while preserving the integrity and defensibility of investigations. Code: FDB1602

Curriculum

Core Regulatory Expectations for Investigations and CAPA
10 min
How AI Is Being Used in CAPA and Investigation Workflows
8 min
Where AI Output Conflicts with Evidence-Based Requirements
10 min

Requirements

  • Working in FDA-regulated industries (pharma, biotech, medical device)
  • Familiarity with CAPA systems, deviation management, or quality investigations
  • Applicable to QA, compliance, regulatory affairs, and manufacturing quality professionals

Who Should Attend

CAPA Owners, QA Investigators, Quality Assurance Managers, Compliance Specialists, Regulatory Affairs Professionals, Manufacturing Quality Leads.

Areas Covered

Role of AI in CAPA and Investigation Processes
Regulatory Expectations for Investigations
Acceptable vs. High-Risk AI Use Cases
Risks in Root Cause Analysis and Causal Reasoning
Bias and Limitations in AI-Generated Outputs
Maintaining Evidence-Based Conclusions
Human Oversight and Accountability
Verification and Review Requirements
Integration into CAPA Workflows
Practical Control Framework

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
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1

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$190.00
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Certificate of completion

Event Details

Format

Live Webinar

Duration

1 hour

Certificate

Included

Date

Monday, July 13, 2026

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