Important aspects of sterile filtration are the qualification of the filter, the validation of the filtration process and the execution of filter integrity tests. Sterile filters must be sterilized before use. After filling a batch, at the latest after one working day, the sterile filter should be disposed of. For small batches, reuse as a pre-filter can be considered for cost reasons but requires appropriate validation.
[GMP Compliance Adviser, Chapter 12.E]
You can find out more about this topic:
The GMP Compliance Adviser is the world's largest knowledge portal for quality management in the pharma business!