Outlier consideration and re-dosing of Subjects [Regulatives / Guidelines]

posted by tripathy – 2006-07-21 08:06 (6487 d 06:36 ago) – Posting: # 180
Views: 7,065

Dear Forum member,

I am a Pharmacokinetist. I am new to this forum.
I went through some of the discussion topics, I found them really useful and decided to become a member of this forum.

I would like to ask forum members regarding the Statistical outlier consideration and re-dosing of subjects in a BE study. Whether outliers and re-dosing of subjects are acceptable by US-FDA regulatory, if yes then I would be very greatful to you if you provide me the link to any such guidance or correspondance from US-FDA.

Thanks and Regards,
Tripathy

Complete thread:

UA Flag
Activity
 Admin contact
22,993 posts in 4,828 threads, 1,658 registered users;
72 visitors (1 registered, 71 guests [including 2 identified bots]).
Forum time: 14:42 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