PK Parameters for Bioequivalent Criteria [Regulatives / Guidelines]

posted by omprakash – India, 2017-01-23 13:21 (2648 d 10:58 ago) – Posting: # 16993
Views: 6,619

Dear Sir,

We have developed Paracetamol Sr 665mg tablets (Unilayer) versus Panadol 665mg tablets (bilayer, 31% IR + 69% SR).

Then what will be the primary PK parameters for Bio-equivalent criteria. Whether Cmax also compulsory to meet Bio-equivalent criteria then what will be the acceptance criteria. OR Only AUC is required as Bio-equivalent criteria?

Regards,

Om Prakash

Complete thread:

UA Flag
Activity
 Admin contact
22,993 posts in 4,828 threads, 1,656 registered users;
84 visitors (0 registered, 84 guests [including 3 identified bots]).
Forum time: 01:20 CEST (Europe/Vienna)

So far as I can remember,
there is not one word in the Gospels
in praise of intelligence.    Bertrand Russell

The Bioequivalence and Bioavailability Forum is hosted by
BEBAC Ing. Helmut Schütz
HTML5