Investigation of Out-Of-Specification Laboratory Results 2017 is a webinar that covers topics such as:
- The FDA model for handling OOS investigations
- Why the regulators are concerned about the handling of OOS investigations
- How the laboratory can meet regulatory expectations for OOS investigations
- Commonly accepted terminology such as repeat testing and retesting
- The interaction between the laboratory and other units in the organization
Investigation of Out-Of-Specification Laboratory Results 2017 is intended for:
- Laboratory Analysts
- Laboratory Supervisors
- Quality Assurance Record Reviewers
- Quality Assurance Managers
