regulatory guideline [Regulatives / Guidelines]

posted by wock – India, 2023-05-22 08:06 (132 d 22:54 ago) – Posting: # 23563
Views: 588

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

Complete thread:

UA Flag
 Admin contact
22,763 posts in 4,775 threads, 1,628 registered users;
9 visitors (0 registered, 9 guests [including 2 identified bots]).
Forum time: 07:01 CEST (Europe/Vienna)

The object of statistics is information.
The objective of statistics is the understanding of information
contained in data.    Irwin and Marylees Miller

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