It is a regulatory requirement for pharmaceutical companies to perform Instrument Validation on new equipment, and regular Requalification on existing equipment. In brief, Instrument Validation is a fully documented process that ensures the instrument is working correctly.
It demonstrates that the measuring instrument is working correctly and hence has no detrimental effect on the quality of the analytical results. For industries which are not as heavily regulated annual calibration (as previously described) would be sufficient to demonstrate that the instrument is working correctly.
Reagecon’s Technical Services Department has developed calibration and validation protocols for a wide range of pH instruments. This service can be performed at the customers’ premises, or alternatively the instrument can be sent to Reagecon for calibration in our purpose-built Metrology Laboratory.
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