FDA and EU Process Validation and Equipment Qualification 2019 is a seminar that covers topics such as:
- General Aspects of Qualification
- Regulatory Requirements and Expectations for Equipment Qualification
- Performance Qualification and Process Validation
FDA and EU Process Validation and Equipment Qualification 2019 brings together:
- Regulatory Affairs Departments
- Quality Departments
- Engineering Departments
- Compliance Departments
- Production Departments
- Manufacturing Departments
- Validation Teams
- Operations Departments
- Process Owners
- Design Engineers
- Internal Auditors