Bioanalytical Methods [Regulatives / Guidelines]

posted by Dr sridevi – India, 2013-06-18 16:51 (4757 d 14:58 ago) – Posting: # 10809
Views: 2,626

Is it necessary to have method development and full validation report before intiation of study for ANVISA submission

Complete thread:

UA Flag
Activity
 Admin contact
23,655 posts in 4,993 threads, 1,572 registered users;
257 visitors (0 registered, 257 guests [including 18 identified bots]).
Forum time: 07:49 CEST (Europe/Vienna)

The real struggle is not between the right and the left
but between the party of the thoughtful
and the party of the jerks.    Jimmy Wales

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