In this Laboratory Investigation training learn what constitutes an OOS observation, what are the guidance's process & 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.
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.
Areas Covered in the Seminar:
- Regulations and Guidances that will be covered (FDA, EU, Canada, WHO, ICH, other).
- FDA Guidance to the Industry: Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
- Q7; 11.1
Who Will Benefit :
The following individuals or disciplines will benefit from attending this Webinar:
- Quality Control Managers
- Quality Control Supervisors
- Quality Control Analysts
- Quality Control Record Reviewers
- Quality Assurance Managers
- Quality Assurance Supervisors
- Quality Assurance Record Reviewers
For More Information: