Cleaning Validation

To ensure the absence of previously manufactured pharmaceutical products from your production equipment, we use suitable analytical techniques. The QACS Laboratory quality assurance approach starts from the preparation of a suitable protocol to the qualification of analytical results.


What we test for

Cleaning validation is important in the pharmaceutical industry. We have developed and implement a microbiological method validation protocol, to document method suitability.

We use high-performance liquid chromatography (HPLC) to ensure that the routine cleaning process you perform on your manufacturing equipment removes all residues of the previously manufactured product.

In HPLC assay verification, we validate linearity, intermediate precision, recovery and specificity.

Some of the equipment we test include the preparation and storage tanks, the filling nozzles and the instruments.

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