Sterile Filtration of Pharmaceutical Products Validation and Regulatory Requirements 2019 is a webinar that covers topics such as:
- Sterility assurance of sterile filtration
- Sterile filtration—importance of quality
- Discussion of different filtration media properties and retention mechanisms
- Sterile filtration system design
- Validation of sterile filter systems
- Methods for sterilization of filters
- Integrity testing
- Microbial retention challenge testing
- Extractable/leachable testing
- Product compatibility testing
- FDA/EU GMP regulatory requirements
Sterile Filtration of Pharmaceutical Products Validation and Regulatory Requirements 2019 is intended for:
- Environmental Monitoring Departments
- Quality Assurance Departments
- Manufacturing Departments
- Microbiology Departments
- Engineering Departments
- Validation Departments
- Maintenance Departments