Laboratory Compliance 2012 - Laboratory Investigation Out-of-Specification Results
Date2012-04-26
Deadline2012-04-26
VenuePalo Alto, USA - United States
KeywordsOut of Specification results compliance training; OOS compliance training; laboratory compliance training; laboratory investigations; OOS results lab processes; FDA Laboratory regulations compliance
Topics/Call fo Papers
In this 90-minute training on laboratory Out-of-specification (OOS) investigations, you will learn what constitutes an OOS observation, what is the OOS investigation process described in the OOS guidance and steps to be taken in the laboratory in the event of an OOS observation.
Why Should You Attend:
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.
Other CFPs
- System Based Inspections - Laboratory Controls
- Laboratory Investigations for Out of Specification Results
- Archiving GLP Records: How Archiving Makes or Breaks the Audit
- Effective & Legal Documentation : If It Wasn’t Documented, It Didn’t Happen
- Foreign Manufacturing Facilities ? Avoiding Problems with FDA
Last modified: 2012-02-24 15:14:49