LABORATORY COMPLIANCE 2011 - Laboratory Investigation Out-of-Specification Results

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Category Laboratory,conference,event,Webinar

Deadline: March 10, 2011 | Date: March 10, 2011

Venue/Country: Palo Alto, U.S.A

Updated: 2011-02-14 18:38:18 (GMT+9)

Call For Papers - CFP

Inadequate procedures for laboratory Out-of-specification (OOS) investigations remain high on the list of FDA observations. The FDA has issued a guidance on the topic, OOS procedures and investigations are still a topic of FDA Investigator review and findings. An out-of-specification laboratory observation triggers emotional and political actions that inhibit a productive investigation with a timely conclusion.

There is still confusion in the laboratories as to how an out-of-specification result should be handled and investigated. In this webinar we will discuss the investigation that goes on within the laboratory. Although the focus will be on the FDA Guidance, the discussion will include suggestions for a process that will meet the FDA expectations.

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