wock
☆    

India,
2023-05-22 08:06
(772 d 23:27 ago)

Posting: # 23563
Views: 2,181
 

 regulatory guideline [Regulatives / Guidelines]

In bioequivalence study if any adverse event is ongoing; we can collect safety sample or end study sample before completion of adverse event. if any reference guideline pls show
UA Flag
Activity
 Admin contact
23,425 posts in 4,928 threads, 1,683 registered users;
40 visitors (0 registered, 40 guests [including 13 identified bots]).
Forum time: 07:34 CEST (Europe/Vienna)

You can do one of two things; just shut up,
which is something I don’t find easy,
or learn an awful lot very fast,
which is what I tried to do.    Jane Fonda

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