Filtration Sterilization Validation
Filter Testing evaluates a filter’s ability to filter out microbial organisms of various sizes. This test allows manufacturers to determine membrane pore sizes and is an excellent lot release test. Test data can also be used as an effective marketing tool. Nelson Laboratories has significant experience using a wide range of microorganisms, working with multiple industries and performing tests in compliance with both the ASTM F838-05 and HIMA guidance documents.
- PDA Technical Report 26
- FDA Guidance for Industry on Aseptic Processing
- AAMI/ISO 13408
Standard turn around times (TAT) are listed below. Ask an expert for a specific consultation on your product. If you are ready to submit your samples for testing, click here to fill out the Sample Submission Form.
|Code||Test||TAT (days)||Request Quote|
|FSV210||Filter Sterilization Validation: PDA Technical Report 26||75||Add|
|FSV220||Filter Sterilization: Filter extractables test (NVR and FTIR)||0||Add|
|FSV230||Filter Sterilization: Integrity test value (product wet integrity) validation||0||Add|
|FSV240||Filter Sterilization: Compatibility test for filters||0||Add|
FSV210 - Filter Sterilization Validation: PDA Technical Report 26
TAT: 75 days
FSV220 - Filter Sterilization: Filter extractables test (NVR and FTIR)
TAT: 0 days
FSV230 - Filter Sterilization: Integrity test value (product wet integrity) validation
TAT: 0 days
FSV240 - Filter Sterilization: Compatibility test for filters
TAT: 0 days
FSV210: 3 filters, one from each of three lots
FSV220: 1 full scale filter
FSV230: 1 full scale filter. Product Amount: Per effective filtration area, (e.g. 1,000 cm2 = 1 L product)
FSV240: 2 full scale filters and products
Study OutlineFor the Filter Test study, the organism is grown in a minimal media or other appropriate media depending on the required growth conditions, size ranges needed challenge organism and concentration. The test objective of a most severe bacterial challenge to the filter is met by the challenge conditions which include high pressure, high flow rates and a high bacterial concentration per cm2 of EFA (effective filtration area). The growth parameters, temperatures and media are adapted from the ASTM and HIMA methods.
Each test filter is challenged with a suspension of the specified challenge organism, usually B. diminuta for a 0.2 micron membrane, S. marcescens for a 0.45 micron membrane or Mycoplasma for a 0.1 micron membrane cultured to maximize the percentage of organisms capable of passing through the selected positive control filter (typically a 0.45 µm filter is used for B. diminuta, and other membrane sizes are used for other sized organisms).
Sufficient volume of this challenge suspension is used to provide the correct concentration of organism for the effective filtration area (EFA) of each filter (typically equivalent to at least 1 x 107 colony-forming units (CFU) per cm2 for B.diminuta; this may vary with other challenge organisms).
The challenge will be conducted at a high flow rate and a maximum differential pressure (typically 30 psig). The effluent will be collected and assayed quantitatively. Integrity testing is performed before and after the bacterial challenge procedure.
Please provide the effective filtration area of the filter when submitting samples.