 | Retention testing is required to validate retention of sterilizing-grade membrane filters with specific pharmaceutical preparations. Millipore’s Validation Sciences Laboratories conduct testing on a lab-scale using scaleddown processing conditions such as batch volume and flow rate. After preliminary studies with the candidate process fluid, a test protocol is submitted to the client. Millipore and the client sign the project specific test protocol prior to the start of testing. A standard report summarizing testing data is submitted to the client after completion of testing, and a copy of the raw data is provided with the final report.
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