Properly Investigating and Remediating OOS Results

Date : 17th November 2020 to 17th November 2020

Place : United States, Palo Alto

Website :https://www.complianceonline.com/handling-oos-test-results-and-completing-robust-investigations-webinar-training-704351-prdw

Contact Person:Ashutos Swain

Description:

This webinar will review the regulatory requirements for investigating an OOS Investigation. The responsibilities of the analyst, the supervisor and QA will be discussed. A detailed flow chart will be used to help the attendees clearly understand the steps and the order in which they are to be performed. The structure of an Investigation report which properly documents the investigation will be discussed. The lack of or Inadequate procedures for handling out of specification (OOS) situations and failure investigations are amongst the most frequently found deviations in FDA warning letters. Most companies have procedures but either they are not adequate or are not followed. This seminar will guide attendees through the entire process from detection an out-of-specification result to informal and formal laboratory and batch investigations.

Properly Investigating and Remediating OOS Results will be held in Palo Alto,United States on date 2020-11-17

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Deadline for abstracts/proposals : 7th November 2020

Keynote Speakers :

Check the event website for more details.