When: |
24 Feb 2022 | |
Where: |
Online Event | United States | |
Website URL: |
https://www.complianceonline.com/human-errors-gmp-manufacturing-laboratory-processes-webinar-training-706786-prdw?channel=Brownwalker | |
Sponsoring organization: |
Compliance Online | |
Categories: |
Medicine & Health - Pharmaceutical / Medicinal |
Keywords:
Event description:
This instructor-led live training webinar will discuss regulatory requirements for detecting, correcting and preventing human errors in manufacturing and laboratory environments as well as developing a competent, effective corrective and preventive action system.
Why Should You Attend:
Analysis of investigation reports reveal that human error is one of the top root causes for deviations, discrepancies and quality incidents in pharmaceutical manufacturing. And when you examine the CAPA's that are developed from these, retraining and rewrite of SOP is top the list. Yet on further re-examination, you find that these problems keep resurfacing again and again. Put in another way, the CAPA's are ineffective. Does it mean that the CAPA's were wrong or is it pointing to another problem? Namely, that the investigation did not pinpoint the root cause of or most probable contributing factors to the problem. Most often "human error" is not really the problem but a symptom of a system or f...
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Posting date:
01 February 2022 | 238 views
Placement:
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