CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectations

  • 26 Jun 2019
  • Webinar

Description

CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectations is a webinar that covers topics such as:

  • The Basic Steps to Problem Solving
  • Regulatory "Hot Buttons"
  • ID / Document the Problem -- CAPA, et al
  • A Suggested Investigation Template
  • Use the 7 Tools to Find the Solution(s)
  • Failure Investigation / Analysis Methodology -- And One Possible Template
  • Lock In the Change - Close the Loop
  • Monitor for Effectiveness
  • Take It to the Next Level

CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectations brings together QA, Senior management in Drugs, Devices, Biologics, Dietary Supplements, R&D, RA, Production, Engineering, Consultants; others tasked with product, process, CAPA resolution, failure investigation responsibilities and Operations.

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Important

Please, check "CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectations" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Healthcare, Medical device, Medical laboratories, Pharma

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