multilayer tablet exclusion criteria from PK analysis due to emesis [Regulatives / Guidelines]

posted by Mahesh M – India, 2016-01-08 11:56 (3825 d 21:41 ago) – Posting: # 15803
Views: 7,297

Dear All,

My concern regarding multilayer tablet one API is IR and another is XR (combination of IR and XR) what is the exclusion criteria of subjects form PK analysis due to the emesis for FDA submission? Can we use different criteria for IR and XR as per FDA guidance or this combination product consider as modified release dosage form?

Regards
M

Complete thread:

UA Flag
Activity
 Admin contact
23,656 posts in 4,994 threads, 1,570 registered users;
282 visitors (0 registered, 282 guests [including 25 identified bots]).
Forum time: 10:38 CEST (Europe/Vienna)

It requires a very unusual mind
to undertake the analysis of the obvious.    Alfred North Whitehead

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