Apply technical writing tips to writing investigation problem statements, RCA, and CAPA; to more clearly document and better resolve nonconformities.
Explain CAPA system elements and FDA expectations.
Explain how Risk Assessment tools can be used to determine priority and significance of CAPA.
List different Root Cause Analysis tools and resources.
CAPA Definitions and Approaches
Example CAPA forms
CAPA Regulatory expectations (drugs, biologics and medical products)
Pharmaceutical Quality System Guidelines (ICH Q10) and product lifecycle approach
Quality Risk Management (ICH Q9) and risk assessment (RA) approaches to CAPA, including Fault Tree Analysis (FTA), Hazard Analysis and Critical Control Points (HACCP), Hazard and Operability Analysis (HAZOP), Failure Modes Effects Analysis (FMEA)
Failure Modes, Effects, and Criticality Analysis (FMECA)
Sources of CAPA
FDA Inspection Observations (FDA Form 483)
Technical Writing tips for clarity and completeness
Investigations/ Problem/Event Statements and summaries
Records/Sources of information/Identification
Root Cause Analysis (RCA) definitions, tools, and approach
CAPA implementation and resolution
8
1
None
None
No
N/A
BioNetwork will provide
None
90% attendance
Additional requirements: N\A
N/A
Manufacture/Production Operators, Team Leaders and Supervisors, Quality Control Personnel, Quality Assurance Personnel, Maintenance/Engineering Personnel
N/A
N/A
Manufacture/Production Operators
Team Leaders and Supervisors
Quality Assurance Personnel
Quality Control Personnel
Maintenance/Engineering Personnel
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Requisites: None
To view information on this course and additional non-degree course offerings, visit the Workforce Continuing Education Catalog