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IQ OQ PQ validations

We perform validation services using certified instruments from ISO 17025 certified laboratories.


The documentation is drawn up and compiled according to GMP standards by highly qualified personnel with many years of experience in the field. At the end of the qualification service, IQ QO PQ protocols are issued, drafted by ALS and shared with the client.

ALS can draw up ad hoc and customized documentation according to customer requirements.


At the end of the service, documentation is issued for each activity (IQ OQ PQ)

The request for this service stems from the customers' need to validate the purchased equipment to objectively demonstrate the performance declared by the manufacturer.

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