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CAPA: Corrective and Preventive Actions and Non-Conformance


OVERVIEW If you only fix the symptoms – what you see on the surface – the problem will almost certainly happen again, which will lead you to fix it, again, and again, and again.
If, instead, you look deeper to figure out why the non-conformance is occurring, you can fix the underlying systems and processes that caused it.
WHY SHOULD YOU ATTEND
• When you have a non-conformance in the laboratory, how do you approach it?
• Do you jump in and start treating the symptoms?
• Do you stop to consider whether there's actually a deeper problem that needs your attention?
AREAS COVERED
• Defining the problem
• Examining the data
• Identifying possible causal factors
• How to conduct a root cause analysis
• When is a CAPA required
• Taking corrective and preventive action
• Verifying the effectiveness of the corrective action
LEARNING OBJECTIVES
Root Cause Analysis (RCA) is a popular and often-used technique that helps people answer the question of why the problem occurred in the first place. RCA assumes that systems and events are interrelated. An action in one area triggers an action in another, and another, and so on. By tracing back these actions, you can discover where the problem started and how it grew into the symptom, you're now facing.
WHO WILL BENEFIT
• Microbiologists
• QA managers
• Laboratory managers
• Laboratory supervisors
• QC practitioners
• Management Controls
Use Promo Code TDES20 and get flat 20% discount on all purchases.
To Register (or) for more details please click on this below link:
https://bit.ly/2QFr6h0
Email: [email protected]
Toll Free: +1-888-300-8494
Tel: +1-720-996-1616
Fax: +1-888-909-1882

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