Veri-Q: for LC and LCMS system verification
Veri-Q is for those pharmaceutical and biotech labs that are not yet GLP/cGMP but want the assurance of data integrity prior to clinical trials.
It’s for those labs that want accurate records established leading into clinical trials and manufacturing. Currently, Veri-Q is available for LC and LCMS systems.
Therapeutics development firm uses Veri-Q
Earlier in the year a therapeutics technology development firm whose science was originally developed by a consortium of scientists from MIT had a Veri-Q conducted on its Waters 2695 Alliance HPLC while currently in the pre-clinical stage of drug development.
Is it for you?
A Veri-Q describes and documents a set of tests performed on the LC or LCMS system hardware. This set of tests verify that the LC or LCMS System functions as specified in this protocol. The protocol ensures that the LC or LCMS functions according to its design, and is capable of producing test results that meet minimum standards of accuracy and precision.
Upon completion of the protocol, a final report is generated, with the raw data and final report securely stored in a specified customer location.
The SOW for LC and LCMS include:
▪ Flow rate accuracy
To learn more about the unique Veri-Q System Verification program, which is part of the Overbrook Total Qualification Process (TQP), contact your Overbrook representative, email@example.com. Or call 855-782-4373 today.
The Overbrook Total Qualification Program (TQP) provides a choice of qualification options for both the GLP/cGMP facility and the pre-clinical laboratory.
For those labs that are GXP, Overbrook Support offers its IQ/OQ/PQ service.