In-vitro equivalence [General Sta­tis­tics]

posted by ElMaestro  – Denmark, 2012-05-19 03:35 (5136 d 10:48 ago) – Posting: # 8587
Views: 6,095

Hi Martin,

which of the following questions are you trying to answer:
1. Can this lot I just produced be released?
2. Is the production process stable?

Without being fully sure I get the idea that your situation isn't classical (batch release is based on floating criteria?) and that you are perhaps entering the world of GMP, Six Sigma, DoE and QbD and then it quickly gets extremely complex. Could you provide a bit more context?

Pass or fail!
ElMaestro

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