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KB004922 : What are the Verification Regulations (e.g. Verification Item, Method, Period) for the 2100 Bioanalyzer? - 2100 Bioanalyzer Hardware
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What are the Verification Regulations (e.g. Verification Item, Method, Period) for the 2100 Bioanalyzer?
What are the verification regulations (e.g. verification item, method, period) of 2100 bioanalyzer? FAQ Answer*: This is usually determined by the QA department of the company using the 2100 bioanalyzer. OQ should be performed after installation of hardware or software (after the initial installation), after major events, such as repair, upgrades, or relocation, after any software change that affects system security, data integrity, or administrative controls and at regular intervals during routine use. Details are in the OQ/PV protocols, which can be reviewed under CDA if required.
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