Share Your Research, Maximize Your Social Impacts
Main Menu
Searching By
PARTNERS
2021 - Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements
Topics/Call fo Papers
Sterile Filtration - Importance of Quality
Sterility Assurance of Sterile Filtration
Sterile Filtration System Design
Discussion of Different Filtration Media Properties and Retention Mechanisms
Methods for Sterilization of Filters
Validation of Sterile Filter Systems
Microbial Retention Challenge Testing
Integrity Testing
Product Compatibility Testing
Extractable/Leachable Testing
Regulatory Requirements
Sterility Assurance of Sterile Filtration
Sterile Filtration System Design
Discussion of Different Filtration Media Properties and Retention Mechanisms
Methods for Sterilization of Filters
Validation of Sterile Filter Systems
Microbial Retention Challenge Testing
Integrity Testing
Product Compatibility Testing
Extractable/Leachable Testing
Regulatory Requirements
Other CFPs
- Applied Time Series Analysis in Healthcare
- How to Survive a DEA Inspection Series: For DEA Registered Analytical Labs and Research Facilities
- Non Resident Alien Payee (1042-S, W-8) - How to Handle the Information Reporting and Backup Withholding Requirements of the IRS
- CGMP controlled Raw Materials
- AML Model Validation: A Critical Need in the New Regulatory Environment
Last modified: 2021-10-31 00:18:44