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IQ is for installation qualification, OQ is for operational qualification and PQ is for performance qualification. They represent quality assurance protocols that the customer has to follow during each phase of the manufacturing process, especially for pharmaceutical equipment. As pharmaceutical industry is regulated by FDA rules, it is essential to complete IQ, OQ and PQ protocols.

Our worldwide distributors can offer the Installation Qualification (IQ) and Operational Qualification (OQ) on side to verify that your instrument is working according to the official specifications.

I.Q. INSTALLATION QUALIFICATION – O.Q. OPERATIONAL QUALIFICATION – P.Q. PERFORMANCE QUALIFICATION
These Documents have the target to verify that the instrument is working according to the supplier specification, during the installation and during the working activities.

METHOD
Read the pages of the document

ACCEPTANCE CRITERIA
Each pages of this document is based on a specific criterion that should be followed

These Documents have the target to verify that the instrument is working according to the supplier specification, during the installation and during the working activities.

  • Do the actions described in the pages of this Document
  • Answer YES or NO to the questions present in each page
  • Insert comments and corrective actions where they are applicable
  • Date and sign each page when it has been completed
  • Record the results each time a page of the Document has been completed
  • Sign, date and register the document once it is fully completed
Code IQ, OQ, PQ Family
497 IQ, OQ, PQ documents for CFU Photo Camera
499 IQ, OQ, PQ documents for TRIO.CPS
500 IQ, OQ documents for MINI
501 IQ, OQ documents for MONO
502 IQ, OQ documents for DUO, TRIO, ISOLATOR, AIRBIO ONE, AIRBIO DUO
509 IQ, OQ documents for TRIO.GAS
505 PQ documents for MINI
506 PQ documents for MONO
507 PQ documents for DUO, TRIO, ISOLATOR, AIRBIO ONE, AIRBIO DUO
508 PQ documents for TRIO.GAS
515 IQ, OQ documents for VERITEST
516 PQ documents for VERITEST