average bioequivalence [Regulatives / Guidelines]

posted by Mahmoud  – Jordan, 2024-06-24 13:29 (321 d 16:11 ago) – Posting: # 24035
Views: 2,090

Dear All

For statitical anaylsis Semi-Replicated (TRR,RTR,RRT). Some pesrons do the followings:

model= Sequence Period Treatment Sequence*Treatment as fixed effects.

Random : Subject(Sequence) Treatment*Subject(Sequence).

CI for T/R ratio derived using Treatment*Subject(sequence) as the error term.


Is this true under FDA or EMA guidelines.

Complete thread:

UA Flag
Activity
 Admin contact
23,424 posts in 4,927 threads, 1,671 registered users;
84 visitors (0 registered, 84 guests [including 9 identified bots]).
Forum time: 05:41 CEST (Europe/Vienna)

If you shut your door to all errors
truth will be shut out.    Rabindranath Tagore

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