bioanalytical validation runs [Bioanalytics]

posted by samar sameh – Jordan, 2017-12-21 09:38 (3100 d 02:51 ago) – Posting: # 18071
Views: 6,305

Dear freinds
i have a question related to the bioanalytical validation runs:
According to EMA and FDA guidlines, should we include quality control samples in each validation run (matrix effect, Reccovery, stability,,, )?


Edit: Category changed; see also this post #1. [Helmut]

Complete thread:

UA Flag
Activity
 Admin contact
23,654 posts in 4,992 threads, 1,570 registered users;
195 visitors (0 registered, 195 guests [including 18 identified bots]).
Forum time: 13:30 CEST (Europe/Vienna)

Scientists often have a naïve faith that
if only they could discover enough facts about a problem,
these facts would somehow arrange themselves
in a compelling and true solution.    Theodosius Dobzhansky

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