Human Error and Documentation Practices in Good Laboratory Practices (GLP)
Navigate human error, documentation pitfalls, and GLP requirements — learn how accurate record-keeping supports data integrity, research reproducibility, and regulatory compliance.
Instructor
Charles H. Paul
President, CHP Consulting LLC — Regulatory Compliance & Operational Excellence
What You'll Learn
About the event
About this event
The webinar empowers participants to navigate the nuanced terrain of human error and documentation practices. Regulatory guidelines and requirements related to documentation in GLP are demystified, highlighting the vital role that meticulous documentation plays in maintaining compliance and navigating audits.
In the realm of scientific research, the symbiotic relationship between human error, documentation practices, and Good Laboratory Practices (GLP) is pivotal for maintaining the integrity and trustworthiness of experimental outcomes. Precise and comprehensive documentation serves as a crucial antidote to the vulnerabilities of human fallibility.
Code: FDB3765
Curriculum
Requirements
- Laboratory scientists, researchers, QA/QC professionals, and lab managers
- Applicable to regulatory affairs specialists, compliance officers, and auditors in life sciences
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
1.5 hours
Certificate
Included
Access
Lifetime
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