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Column Performance.

Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.

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Hello All;
I have a issue with my columns, we are trying to develop a standart procedure for criteria of when you have to regect a column or when you need to Regenerate it; I know thres is now a Standart procedure but I suposse that may be USP or FDA have a criteria bese on N; Taling, selectivity; that we can use to determine when we have to get a new column or do a regeneration.
Usually I develop the method and not concern about this; but now I have to help this this.

I will Appreciate you advices.

Thanks and Best Regards.

As far as I know, there is no "one size fits all" standard. If you are dealing with a validated, regulatory method, you should have system suitability criteria for that method. When you no longer pass system suitability, the column is no longer suitable :wink: .

The FDA "suggestions" for system suitability date back to 1987 and are, in my opinion, only there as examples (N > 2,000 !).
-- Tom Jupille
LC Resources / Separation Science Associates
tjupille@lcresources.com
+ 1 (925) 297-5374
2 posts Page 1 of 1

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