WELCOME TO ENTERPRISE EDITION
Whether you have purchased a new Agilent instrument and are experiencing Agilent compliance services for the first time, or are upgrading from Classic Edition qualification services, there are four easy steps for perfect delivery of your first Enterprise Edition IQ and OQ services.
Step 1: Review the Equipment Qualification Plan (EQP)
The Standard EQP documents provide the protocol information that you’ll need to approve Agilent Enterprise Edition IQ & OQ for your lab. Inside you’ll find a list of tests including their set-points and limits for the standard service delivery.
Standard EQP Review Document for LC Systems
Standard EQP Review Document for UHPLC Systems
Standard EQP Review Document for LCMS Systems
Standard EQP Review Document for UHPLC-MS Systems
Standard EQP Review Document for GC Systems
Standard EQP Review Document for GCMS Systems
Standard EQP Review Document for Software
Note: Should you wish to configure an EQP with other specific set-points and limits or add additional, optional tests, please email a detailed request to enterprise_edition@agilent.com
Step 2: Approve the EQP for Use
Print the Equipment Qualification Plan to paper and keep the ink-signed approval page for your own records. Or for electronic storage, simply use Adobe Acrobat digital signature. You only have to approve the EQP one time , at the first delivery. We’ll deliver your approved protocol every time from then on.
Step 3: Confirm Your Approval of the EQP Prior to the Scheduled Visit
When the Agilent representative contacts you to schedule your compliance service visit, simply give verbal confirmation that you approve the Equipment Qualification Plan. Your approval is required in order for our representative to schedule your service visit.
Step 4: Review Your Results in the Equipment Qualification Report
When your engineer finishes the qualification testing, you’ll immediately receive an equipment qualification binder with a CD containing all your Equipment Qualification Reports (EQR). Its secure PDF format is accepted by the FDA and other major regulatory organizations and can be approved with a single signature. You can also produce paper records, should you prefer to print and sign a copy of your report.
Please see the Agilent Enterprise Edition website or contact your Agilent Sales Representative for additional information. |