wock
☆    

India,
2023-05-22 08:06
(779 d 19:37 ago)

Posting: # 23563
Views: 2,190
 

 regulatory guideline [Regulatives / Guidelines]

Post reply
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
23,428 posts in 4,929 threads, 1,689 registered users;
64 visitors (0 registered, 64 guests [including 18 identified bots]).
Forum time: 03:44 CEST (Europe/Vienna)

To know that we know what we know,
and to know that we do not know what we do not know,
that is true knowledge.    Nicolaus Copernicus

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