Conducting Effective Out-Of-Specification (OOS) Investigations

Venue: Holiday Inn Somerset

Location: Somerset, New Jersey, United States

Event Date/Time: Aug 20, 2009 End Date/Time: Aug 21, 2009
Registration Date: Aug 19, 2009
Early Registration Date: Jul 20, 2009
Report as Spam


A Two-day Interactive Course & Workshops Featuring:

Regulatory Expectations for Compliant OOS Procedures
Developing the OOS System as Part of Your Quality Program
Review of FDA's latest Guidance on OOS/OOT
Warning Letters from FDA 483's - Case Studies
Defining OOS/OOT Results
Implementing Proper OOS Management
Common Mistakes and Pitfalls when Conducting an OOS Investigation
Conducting OOS/OOT Investigations and Evaluating results
Differentiating Responsibilities of Laboratory Analysts and Supervisors
Testing Types to Determine the Validity of an OOS
How to Handle Retests when Investigations are Inconclusive
Tracking and Trending Lab Investigations
Using a Checklist Approach to Determine Sources of Error
Product Impact when Documenting Out-of-Trend (OOT) Results
Types of required tests to determine the validity of the OOS
Determining Re-testing and Re-Sampling Frequency
Root Cause and CAPA Strategies
Developing OOS Investigation Procedure and Forms


195 Davidson Avenue
New Jersey
United States