Quality Management Series
This four-part series provides a foundational understanding of quality management and its integral role in the functions of an efficient, well-run laboratory.
This four-part series provides a foundational understanding of quality management and its integral role in the functions of an efficient, well-run laboratory. Part I defines quality management and describes its benefits. Documents and records – the pillars of an effective QMS – are examined in Part II. Part III addresses nonconforming work and deviations, offering insight on how both should be addressed. Finally, Part IV differentiates between corrective and preventive action, placing each in context with regard to the QMS.
Here are all the courses that are included in your bundle.
On-Demand
$99
On-Demand
$99
On-Demand
$99
On-Demand
$99
By the end of this course, you should be able to:
Recognize key quality management terms
Articulate the benefits of quality management systems
Distinguish between documents and records
Identify good laboratory practices
Recognize the link between good laboratory practices and data defensibility
Define nonconforming work and deviations, and properly address both
Differentiate between corrective and preventive action
Understand CAPA’s role in the QMS
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Jeanné Mensingh, Labtopia co-founder, is a Senior Consultant and Instructor for Labtopia Solutions and Labtopia Training. She has extensive experience in regulated industries and all aspects of laboratory operation, from the analytical bench, QA management, plant operations, and commercial laboratory environments.
A natural storyteller, Jeanné has a gift for retaining the interest of her learners, notably when sharing her true life experiences from the laboratory trenches.