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- Posts: 4
- Joined: Mon Sep 05, 2011 8:03 am
The System suitability test when we determine the related substances in a drug according to pharmacopoeia is usually resolution check. As long as a resolution of API peak and an impurity peak is higher 1.5 for example, we can run the sequence.
But how do we know that the system is stable or not without injecting a set of samples?
How about your lab?
Thank you!