Date :
Place : United States, Clyde
Website :https://worldcomplianceseminars.com/
Contact Person:WCs Conference
Description:
Deviations and Non-conformances are enviable. The key is utilizing those events as an avenue to improve the overall quality system. Thorough Root Cause Analysis is essential to correcting and preventing issues. RCA is a systematic approach that utilizes quality tools to objectively identify factors that have resulted in or could contribute to a deviation. Once the RCA identifies the factors that caused the event, proper generation of CAPA actions is critical to maintaining a healthy quality system. The regulatory agencies fully expect to see documented root cause analysis that resulted in both corrective and preventative actions.Deadline for abstracts/proposals : 4th March 2021
Organized By :WOrldcomplianceseminars
Keynote Speakers : Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations.
Conference Highlights :Part 1 – How to Perform a Thorough Root Cause Analysis (RCA) • Understand Regulatory and Industry Guidance • What is Root Cause Analysis? • When Should Root Cause Analysis be performed? • Discuss several Root Cause Analysis Methodologies • Discuss common errors that occur during RCA Part 2 – Developing Appropriate Corrective and Prevention Actions (CAPA) • Understand Regulatory and Industry Guidance • Discuss the difference between Correct
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