Investigating Out-Of-Specification (OOS) Test Results for Pharmaceutical ProductionLive Web Seminar

Venue: Online

Location: Montreal, Quebec, Canada

Event Date/Time: Sep 20, 2007 End Date/Time: Sep 20, 2007
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Description

Speaker:
Lic. Johnny Guerra
Industry Consultant / President, Guerra Consulting Group Inc.


In October 2006, the FDA released the OOS final guidance document titled “Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production”. This document provides guidance to the pharmaceutical industry pertaining to the investigation process for occurrences where laboratory results fall outside of specification limits. Due to controversies and much discussion, this new guidance replaced the draft guidance from September 1998, which was one of the most important guidance documents followed by FDA Investigators and Industry peers.

During this 2 hour presentation, Lic. Johnny Guerra will address the requirements for investigating OOS results in the laboratory area, including responsibilities of the analyst and supervisor, as well as the extension of the investigation to manufacturing processes and raw materials. The presentation will also discuss the interpretation of investigational results and a firm’s Quality Control Unit responsibilities when concluding the investigation process.

Topic:
"Investigating Out-Of-Specification (OOS) Test Results for Pharmaceutical Production"
• An overview of the final FDA guidance document
• What FDA Auditors look for in terms of human errors
• The responsibilities of laboratory analysts and supervisors
• When the validation of the analytical method should be evaluated
• When a full investigation should be triggered
• Types of required tests to determine the validity of the OOS
• When and how often to conduct re-testing and re-sampling
• Assessing the product impact when documenting out-of-trend (OOT) results
• The essence of corrective and preventive actions plans (CAPA)

Learning Objectives:

• Understanding the responsibilities of laboratory analysts and supervisors
• Awareness of what the FDA will be looking for in terms of Human Errors
• Understanding when a full investigation should be triggered
• Learning when to evaluate the validation of analytical methods
• Knowledge of testing types required to determine the validity of an OOS
• Understanding the frequency with which to conduct re-testing and re-sampling
• Comprehension of the product impact when documenting out-of-trend (OOT) results
• Understanding the essence of corrective and preventive action plans (CAPA)


Who Should Attend:

• Pharmaceutical Production
• Quality Assurance Specialists
• Quality Control Specialists
• Lab Managers/Supervisors
• Lab Analysts

Venue

Online
Montreal
Quebec
Canada
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