Trevor J Henderson
Laboratory Products Group Creative Services Director at Lab Manager
Trevor Henderson BSc (HK), MSc, PhD (c), has more than two decades of experience in the fields of scientific and technical writing, editing, and creative content creation. With academic training in the areas of human biology, physical anthropology, and community health, he has a broad skill set of both laboratory and analytical skills. Since 2013, he has been working with LabX Media Group developing content solutions that engage and inform scientists and laboratorians. He can be reached at thenderson@labmanager.com.
Education
University of Toronto
Doctor of Philosophy Ph.D.(c), Medical Anthropology
University of Toronto
Master of Science (MSc), Physical and Biological Anthropology
University of Guelph
B.Sc Human Kinetics
Articles by Trevor J Henderson
Explore the types of stability chambers, required storage conditions, regulatory guidelines, and validation steps essential for pharmaceutical drug storage and testing.
| 3 min read
Discover how Risk-Based Quality Management (RBQM) enhances pharmaceutical compliance and product quality. Learn key definitions, risk assessment tools, implementation strategies, and regulatory alignment.
| 4 min read
Learn how to prepare for and execute pharmaceutical QC lab audits. Discover types of audits, best practices, and strategies for responding to audit findings.
| 5 min read
Explore how chanterelle mushrooms contribute to kokumi taste through fatty acid derivatives, using UHPLC-MS for compound identification and food quality control.
Updated | 5 min read
Discover how scientists extended fresh pasta’s shelf life by 30 days using innovative packaging and processing methods. Learn what it means for food safety.
Updated | 4 min read
Understand how to manage Out-of-Specification (OOS) results in pharmaceutical manufacturing. Learn about OOS definitions, investigation protocols, regulatory expectations, and corrective action strategies.
| 4 min read
Discover the best practices for batch record review in pharmaceutical manufacturing. Learn about key components, review strategies, common errors, and compliance tips to ensure product quality and regulatory adherence.
| 5+ min read
Explore the fundamentals of Pharmaceutical Quality Assurance (QA), including its definition, scope, objectives, differences from Quality Control (QC), and key roles and responsibilities in regulated environments.
| 5 min read
Managing medical waste in laboratory settings requires a clear understanding of classification, stringent compliance with evolving regulations, and well-defined roles among personnel.
| 4 min read
Explore how pharmaceutical particle size analysis influences drug bioavailability, manufacturing processes, and regulatory compliance.
| 5 min read
Learn how applying Pareto's Rule—also known as the 80/20 Rule—can dramatically improve productivity, focus, and strategic planning across industries.
Updated | 4 min read
Learn how new technologies remove genotoxic impurities from drug ingredients and how FDA and ICH guidelines govern their detection, limits, and control.
Updated | 4 min read
Learn how stability testing of pharmaceuticals supports drug shelf-life, regulatory compliance, and safe, effective product performance across storage conditions.
| 5+ min read
Explore analytical method development and validation, including ICH/FDA guidelines, validation parameters, and lab best practices for reliable results.
| 5+ min read
Explore how dopamine helps the brain avoid bad outcomes and why the popular dopamine detox trend oversimplifies this complex learning process.
| 4 min read
