QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025: The Quality System Manual (QSM) is the bible in a QMS environment because, much like its predecessor, Good Laboratory Practice (GLP), it contains the policies that the laboratory is expected to follow to achieve quality results. It is in fact only the “what to do” component of a QMS. This is the 1st of two webinars on this topic and focuses on complying with themanagement requirements of the standard.
Many laboratories regard Quality Assurance, Quality Assessment and Quality Control as independent activities, others use the terms interchangeably, e.g. QA/QC. This demonstrates a lack of appreciation of the differences between Assurance, Assessment and Control, as well as the interrelationships, particularly between QA and QC. This has created confusion in the minds of many analysts with respect to understanding how QA and QC play separate, but related roles for achieving Quality Assurance in a Quality Management System (QMS).
Management Components of a QMS
Review of Requests, Tenders and Contracts
Subcontracting of Tests and Calibrations
Accommodation and Environmental Conditions
Test and Calibration Methods and Method Validation
Handling of Test and Calibration Items
WHO WILL BENEFIT
Laboratory Quality Development
Laboratory Quality Management
Laboratory Quality Control
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