Introduction to Root Cause Investigation for CAPA

Introduction to Root Cause Investigation for CAPA is a webinar that covers topics such as:

  • FDA and ISO (13485) Requirements
  • What is CAPA vs Correction
  • Steps in a CAPA Process
  • CAPA’s Criticality in Quality Systems
  • Risk Management as Part of CAPA
  • Quality Data Sources for CAPA
  • Challenges Associated to RCA
  • What is a Root Cause Analysis (RCA)/Investigation
  • Six Steps in Problem Solving
  • Difference between a direct cause, a contributing cause and a true root cause
  • Tools Used for RCA/Investigation
  • Steps to Follow If the Root Cause is Not Clearly Known
  • Examples of Three of These Tools and When to Use Them

Introduction to Root Cause Investigation for CAPA is intended for:

  • Quality Assurance/ Quality Control Personnel
  • CAPA Owners
  • Document Control Personnel
  • Regulatory Compliance Professionals
  • Quality and Manufacturing Engineer
  • Regulatory Affairs Professionals
  • Quality Auditors
  • Supplier Quality Managers

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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