Human Error and Documentation Practices in Good Laboratory Practices (GLP): Understanding the Criticality of Accurate and Complete Documentation in GLP

In today's rapidly evolving scientific landscape, the 90-minute webinar titled "Human Error and Documentation Practices in Good Laboratory Practices (GLP)" offers an essential exploration of the critical role that accurate and complete documentation plays in maintaining the integrity of research processes. Delving into the heart of Good Laboratory Practices (GLP), this enlightening session uncovers the intricate relationship between meticulous documentation and the reliability of scientific findings. Over the course of the webinar, attendees will gain a comprehensive understanding of the multifaceted challenges posed by human errors within laboratory environments. With real-world examples, the webinar illustrates the potential consequences of inadequate documentation, underscoring the significance of precise record-keeping in safeguarding data integrity, research reproducibility, and regulatory compliance. Attendees will also glean valuable insights into common documentation errors and pitfalls, as well as invaluable strategies for bolstering documentation practices. From proactive measures and standardized procedures to fostering a culture of clarity and collaboration, participants will leave equipped with the tools to elevate their documentation practices and contribute to the overall credibility of their scientific endeavors.

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The webinar will empower 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 not only maintaining compliance but also in successfully navigating audits. The session fosters an open dialogue, allowing participants to pose questions and seek clarification on the intricacies of the topic. By weaving together theoretical insights and practical strategies, this webinar equips scientists, researchers, and professionals across diverse industries with the knowledge they need to elevate their documentation practices, ultimately bolstering the trustworthiness of their research outcomes and contributing to the advancement of scientific excellence.

Why Should You Attend:

Participating in this training on "Human Error and Documentation Practices in Good Laboratory Practices (GLP): Understanding the Criticality of Accurate and Complete Documentation in GLP" offers participants a unique opportunity to gain essential insights and actionable knowledge. By attending, participants can elevate the integrity and quality of their research through effective documentation practices, reducing the risks of errors and inconsistencies. With a focus on mitigating human error, this training equips attendees with strategies to proactively prevent, identify, and rectify errors, fostering more robust research outcomes. Moreover, participants will grasp the regulatory landscape surrounding GLP and accurate documentation, ensuring compliance and enhancing their ability to navigate audits. The training's emphasis on research reproducibility underscores its value in enabling participants to contribute meaningfully to scientific advancements, while the interactive learning experience ensures practical application of concepts. Ultimately, this training presents a pathway to professional development, equipping participants with skills that enhance their careers and contribute to the broader scientific community.

Areas Covered in the Webinar:
  • Introduction
    • Welcome participants and introduce the webinar's topic and objectives.
    • Briefly explain the importance of Good Laboratory Practices (GLP) in ensuring the quality and integrity of scientific research.
  • Understanding Good Laboratory Practices
    • Define Good Laboratory Practices (GLP) and its significance in various industries, such as pharmaceuticals, biotechnology, and environmental sciences.
    • Highlight the role of GLP in maintaining data integrity, research reproducibility, and regulatory compliance.
  • Human Error in GLP: Causes and Implications
    • Discuss the various sources and types of human errors commonly encountered in laboratory settings.
    • Examine the impact of human errors on research outcomes, data integrity, and regulatory compliance.
  • Importance of Accurate and Complete Documentation
    • Emphasize the role of documentation in ensuring the traceability and transparency of laboratory activities.
    • Explain how accurate and complete documentation supports data integrity, research reproducibility, and regulatory submissions.
    • Discuss the relationship between documentation practices and the credibility of research findings.
  • Common Documentation Errors and Pitfalls
    • Identify and elaborate on common documentation errors, including transcription errors, omission of critical information, and improper data recording.
    • Present case studies or scenarios showcasing instances where documentation errors led to significant problems or delays.
    • Offer practical tips and best practices to mitigate the risk of documentation errors.
  • Strategies for Enhancing Documentation Practices
    • Introduce proactive measures for minimizing human errors in documentation, such as standardized procedures and checklists.
    • Discuss the role of training, awareness, and continuous improvement in cultivating a culture of accurate documentation.
    • Highlight the importance of clear communication and collaboration among team members to ensure consistent and accurate documentation.
  • Regulatory Requirements and Compliance
    • Provide an overview of relevant regulatory guidelines and requirements related to documentation in GLP.
    • Discuss how accurate documentation practices contribute to regulatory compliance and successful audits.
    • Explain the potential consequences of non-compliance with documentation standards.
  • Q&A Session
    • Open the floor for participants to ask questions and seek clarification on the webinar's content.
Who Will Benefit:

Any member of a cross functional project team that has the potential opportunity to lead that project.

  • Laboratory Scientists and Researchers
  • Quality Control and Quality Assurance Professionals
  • Laboratory Managers and Supervisors
  • Regulatory Affairs Specialists
  • Compliance Officers
  • Quality Management Professionals
  • Auditors and Inspectors
  • Biotechnologists and Pharmaceutical Scientists
  • Academic Researchers
  • Environmental Scientists
  • Research Project Managers
  • Laboratory Technicians
Instructor Profile:
Charles H Paul Charles H Paul

President, C H Paul Consulting Inc

Charles H. Paul is the President of C. H. Paul Consulting, Inc. – a regulatory, training, and technical documentation consulting firm. Charles is a management consultant, instructional designer and regulatory consultant and has led C. H. Paul Consulting, Inc. since its inception over 25 years ago. He regularly consults with Fortune 500 pharmaceutical, medical device, and biotechnology firms assisting them in achieving human resource, regulatory, and operational excellence. He is a regular presenter of webinars and on-site seminars in a variety of related subjects from documentation development to establishing compliant preventive maintenance systems. The firm works globally completing projects throughout the EU, UK, South America, and Asia.

Topic Background:

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. Human error, an inevitable facet of scientific endeavors, can range from minor oversights to critical mistakes, potentially introducing inconsistencies and inaccuracies that undermine research credibility. Precise and comprehensive documentation practices emerge as a crucial antidote to the vulnerabilities of human fallibility. Within the context of GLP, meticulous record-keeping serves not only as a chronological record of methodologies and results but also as a cornerstone of transparency and accountability. By reconstructing experiments, facilitating result validation, and establishing an unambiguous data trail, robust documentation bolsters research reproducibility and facilitates the expansion of scientific knowledge.

Good Laboratory Practices (GLP) constitute a robust framework designed to ensure methodological rigor, consistency, and regulatory adherence in laboratory investigations. By emphasizing meticulous planning, execution, and documentation of experiments, GLP aims to preserve data integrity and the well-being of researchers and subjects. Acknowledging the inevitability of human error, GLP underscores the pivotal role of comprehensive documentation practices in reinforcing the trustworthiness of research findings. Effective documentation mitigates the risks of misinterpretation, miscommunication, and data tampering, ultimately elevating the reliability of scientific research across domains such as pharmaceuticals, environmental sciences, and biotechnology. In sum, the synergy between human error, documentation practices, and GLP underscores the significance of rigorous record-keeping in mitigating the challenges posed by human fallibility, fostering research excellence, and upholding the highest standards of scientific inquiry.

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. FDATrainingAlert would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

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