completely new strength [Regulatives / Guidelines]

posted by Clarc Homepage – Romania, 2013-10-18 13:11 (4635 d 02:29 ago) – Posting: # 11693
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Hi all

My problem is related to a generic, whose reference product is 25, 50 and 100 mg. The sponsor however wants to formulate a 35 and 70 mg generic (saying that this way is more effective...??? - I don't want to argue with them...).
Is there a way to obtain approval for the test product based only on bioequivalence? If yes, what kind of design should we use?

Thanks in advance.

I'm always tryin' to do something new, tryin' to look like a beginner.
Meshell Ndegeocello

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