Implementing a Quality Management System
The Quality Management System (QMS) is a set of policies and protocols for the acceptable operation of an organization that contains laboratories that must comply with US FDA GLP. Examples of roles and responsibilities, useful metrics, and tools to monitor performance, and useful documentation will be given.Learning ObjectivesGLP RegulationsQuality Management System (QMS)DefinitionPrinciplesPurposeFunctionElementsQuality PolicyQuality ObjectivesQuality ManualGLP SOPsPlan, Do Check, Act CycleGAP AnalysisQMS Implementation StepsProcess Control and Optimization TheoryProcess CriteriaQuality Audit- Proposed Rule Summary- Cost of QMS- GLP QMS GAP Analysis Checklist- Sample GLP QMS Table of Contents- Example of Process Flow & Criteria- Required GLP SOPs- SOP Template- Seven Tools of Quality Management- Terms: Define & DifferentiateCourse Level - Basic for ImplementationWho Should AttendManagers and supervisors of laboratory organizationsWhy Should You AttendIn 2016, the US Food and Drug Administration proposed basic and wide-ranging changes to its Good Laboratory Practices. This has been published in the Federal Registry: Volume 81 Number 164. The roles of managers, supervisors, and staff are modified and assigned responsibilities are described. The requirements on organizations outside of the laboratory (facilities, sampling, purchasing, training, hiring, and so on) are made inclusive and required for compliance. Recordkeeping and documentation criteria and requirements are described. All of these changes create a very different system from the uppermost level of management downward in the organization chart.
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The Quality Management System (QMS) is a set of policies and protocols for the acceptable operation of an organization that contains laboratories that must comply with US FDA GLP. Examples of roles and responsibilities, useful metrics, and tools to monitor performance, and useful documentation will be given.
Learning Objectives
- GLP Regulations
- Quality Management System (QMS)
- Definition
- Principles
- Purpose
- Function
- Elements
- Quality Policy
- Quality Objectives
- Quality Manual
- GLP SOPs
- Plan, Do Check, Act Cycle
- GAP Analysis
- QMS Implementation Steps
- Process Control and Optimization Theory
- Process Criteria
- Quality Audit
- Proposed Rule Summary
- Cost of QMS
- GLP QMS GAP Analysis Checklist
- Sample GLP QMS Table of Contents
- Example of Process Flow & Criteria
- Required GLP SOPs
- SOP Template
- Seven Tools of Quality Management
- Terms: Define & Differentiate
Who Should Attend
Managers and supervisors of laboratory organizations
Why Should You Attend
In 2016, the US Food and Drug Administration proposed basic and wide-ranging changes to its Good Laboratory Practices. This has been published in the Federal Registry: Volume 81 Number 164. The roles of managers, supervisors, and staff are modified and assigned responsibilities are described. The requirements on organizations outside of the laboratory (facilities, sampling, purchasing, training, hiring, and so on) are made inclusive and required for compliance. Recordkeeping and documentation criteria and requirements are described. All of these changes create a very different system from the uppermost level of management downward in the organization chart.