Read Frequently Asked Questions
Essentials of Sterilizing Grade Filter Validation
This webinar on sterilizing grade filter validation will describe the essential requirements and steps for process validation of sterilizing grade filters. It will discuss multiple guidance documents in regard to sterilizing grade filtration and their interpretation.
Why Should You Attend:
Sterilizing filtration, utilizing membrane filter often of 0.2 micron rating, are critical in aseptic processing. Since biologic drug products are on the rise, which cannot be heat sterilized, aseptic processing and the use of sterilizing grade filters are gaining importance. Filter manufacturers are able to supply filter qualification data, but these results are established under specific lab conditions. To be able to determine the filters performance in the application settings, appropriate process validation (a regulatory requirement) needs to be performed by the end-user of the filter.
This webinar will describe filter qualification activities performed by the filter manufacturer and the resulting data. It will also touch on the guidances mentioned, such as the FDA Aseptic Processing Guidance of 2004, EC cGMP Annex 1 and the PDA’s Technical Report #26, 2008, and the requirements set within. The presenter will follow this with a detailed, step by step description of process validation needs and why these steps are of importance.
Webinar participants will learn about
- The essential requirements of process validation of sterilizing grade filters.
- The details of individual process validation activities.
- The “must have's” of process validation of filters.
- The difference between qualification and process validation.
- Multiple guidance documents in regard to sterilizing grade filtration, the value of the guidances and the interpretation of it.
Areas Covered in the Seminar:
- Filter Qualification.
- Process Validation:
- Viability test.
- Bacteria Challenge test
- Chemical compatibility
- Adsorption analysis
- Extractables analysis
- Particulates Product-wet integrity testing
- Other evaluations
- Questions & Answers.
Who will Benefit:
The following individuals or disciplines will benefit from attending this Webinar:
- Validation management
- Quality assurance and control
- Pharmaceutical and biopharmaceutical processing and manufacturing
- Process development
- Regulatory and Compliance Management
Manufacturers of sterile filters will benefit from this training too.
Mr. Jornitz, has over 25 years of experience and supports the biopharmaceutical industry on a world-wide basis, in particular in process and facility design, single-use technologies, membrane filtration of air and liquids. As Immediate Past Chair of PDA, Jornitz has been part of multiple PDA task forces (TR #26, #40, #41 and#45), committee member (Awards, Journal Editorial, Strategic Planning, Chapter) and committee chair (PDA Annual 2008, Strategic Planning). He is also member of ISPE, DIA and ASTM. Jornitz is the author and co-author of over 100 scientific papers. Additionally he is author and co-author of 9 books, for example Filtration and Purification in the Biopharmaceutical Industry, and 12 book chapters on aseptic process, single-use technologies and regulatory requirements. As faculty member of PDA TRI and Compliance Online, he trains industry members and regulators on a frequent basis. He holds over 30 patents related to single-use equipment, integrity testing and filter housing designs and is the founder of Bioprocess Resources LLC. Mr. Jornitz received his M.Eng. in Bioengineering at the University of Applied Sciences in Hamburg, Germany and accomplished his PED at the IMD Business School, Lausanne, Switzerland.
Sterilizing filtration, utilizing membrane filter often of 0.2 micron rating, are critical in aseptic processing. As soon as heat sterilization cannot be used or bioburden requires to be reduced before heat sterilization, sterilizing grade filters are installed to remove the microbial burden.
To be able to determine the filters performance in the application settings, appropriate process validation requires to be performed by the end-user of the filter. Process validation takes the fluid to be filtered into consideration and the process parameters, used during filtration. Process validation is not only a regulatory requirement, but creates assurance that the filter used is of right choice and performs as expected. Regulatory guidance documents, like the FDA Aseptic Processing Guidance of 2004 and EC cGMP Annex 1 describe filter validation requirements, the most thorough though being PDA’s Technical Report #26, 2008.
ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.
Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.
If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.
We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email firstname.lastname@example.org or call +1-650-620-3937.
This training hasn't been reviewed yet.
Important requirements when validating sterilizing grade filters Introduction and Up-date to Relevant Guidance of Sterilizing Filtration Cell Culture Media Filtration - Points to Consider