Overview:
The objective of this webinar is to develop an understanding of how a compliant laboratory handles the investigation of out-of-specification (OOS) test results and how the laboratory interfaces with other units through the laboratory investigation process. The discussion will be based on the FDA guidance on handling OOS laboratory results.
The objective of this webinar is to develop an understanding of how a compliant laboratory handles the investigation of out-of-specification (OOS) test results and how the laboratory interfaces with other units through the laboratory investigation process. The discussion will be based on the FDA guidance on handling OOS laboratory results.
Speakers
John (Jerry) Lanese,
Who Should Attend
- Laboratory Managers
- Laboratory Supervisors
- Laboratory Analysts
- Quality Assurance Managers
- Quality Assurance Record Reviewers
