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- Posts: 269
- Joined: Fri Jun 29, 2007 1:48 pm
Anyway, the company I am currently working for seems to be getting ready to go down a very awkward path in my opinion. For our impurity methods we are going to have our CDS (Empower) do the integration and peak naming. The individual impurity percents will be pushed into or LIMS system (Labware) where total impurities, total unknown impurities, and total known impurities will be calculated.
Question: Is this a good or a bad idea to have calculations being performed in two different systems such that neither system ever has the complete set of data? I work in a FDA, cGMP, cGLP, et all environment.
It seems to me that the best practice here would be to handle all the calculations in the CDS and then push everything in it's completed and reported state to the LIMS system. But, there is more than one way to skin a cat...