Handling OOS Test Results and Completing Robust Investigations 2019 is a webinar that covers topics such as:
- What the FDA looks for in terms of human errors
- The responsibilities of analysts and supervisors
- The frequency for re-testing and re-sampling
- When a full investigation should be triggered
- How to implement the corrective and preventive action plans (CAPA)
Handling OOS Test Results and Completing Robust Investigations 2019 is intended for:
- Supervisors and Managers in Pharmaceutical or Biological Laboratories
- Lab Analysts
- GMP Auditors
- Regulatory Affairs
- Consultants
- Quality control and Quality Assurance Personnel responsible for Generating or Evaluating test results in a regulated Environment
- Training Departments
