Save time using these fillable Guideline Document packets for qualifying new TRIO.BAS™ instrument. Installation Qualification, Operational Qualification, and Performance Qualification represent quality assurance protocols for each phase of the manufacturing process for pharmaceutical equipment.

• Perform actions described in the document
• Answer the questions present on 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

The IQ, OQ, and PQ process verifies the instrument is working according to supplier specification during the installation and during working activities.