Overview:
This presentation will cover the scope, status and results of the surveillance inspections and what they may mean for the future of 21 CFR Part 11. This will enable you to determine whether your company is subject to the most common violations so you can take action to have a better inspection outcome.
This presentation will cover the scope, status and results of the surveillance inspections and what they may mean for the future of 21 CFR Part 11. This will enable you to determine whether your company is subject to the most common violations so you can take action to have a better inspection outcome.
Who Should Attend
- Everybody Using Computers in FDA Regulated Environments
- IT Manager and Staff
- QA Managers and Personnel
- Regulatory Affairs
- Training Departments
- Consultants
- Validation Specialists
