Manually creating or editing older sample set methods increase the risks of generating incorrect standard curves and standard bracketing, as well as the risks of incorrectly accommodating all samples to be acquired. In this week’s tip, we will discuss how Sample Set Method Templates prevent these risks to reduce and prevent method-related investigations.
You can configure each Validation Protocol method to enforce Approval requirements, Sign off requirements, or both, during various stages of your Method Validation workflow. In this week’s tip, we will continue our discussion on Validation Protocols and learn how to set up Approvals and Sign offs.
In our current series on Validation Protocols, we reviewed Validation Tests that determined whether the ‘chromatographic method’ is valid. In this tip, we’ll discuss a Validation Test that determines whether the ‘chromatographic system’ is valid.
In this week’s tip, we will continue our discussion on configuring tests for the Validation Protocol and learn how to set up the Accuracy Test.
In this week’s Empower tip, we will continue our discussion on Validation Protocols and learn how to set up the Repeatability Test.
A Default String is text that you can create in advance and then select from a list when you are required to provide a reason for creating and/or modifying something in Empower, such as a method. This week, we’ll continue our discussion on Validation Protocols and learn how to create Default Strings.
A Validation Protocol defines the tests to be run, the data to be acquired for each test, and the acceptance criteria for each test. In this week’s tip, we will discuss creating validation protocols in Empower.
Every compliant laboratory must conduct validation studies to show that analytical methods generate accurate and reliable data. The Method Validation Manager (MVM) option for Empower organizes and streamlines the entire method validation process, from start to finish.
Ensuring consistent system preparation before analysis is important to achieve good system and method performance. In this week’s VLOG, we will demonstrate how automating these procedures are used as control strategies.
Identifying and tracking compounds by UV only can result in inaccurate peak assignments and the exclusion of potential key compounds that are non-UV absorbing. Learn how the ACQUITY QDa and Empower address these challenges to improve robust method development and method understanding.