Pivotal study documentation for submission [Regulatives / Guidelines]

posted by Amalia – Greece, 2018-09-24 16:22 (2034 d 04:46 ago) – Posting: # 19299
Views: 1,349

Dear all,

as this is my first post I will try to be as elaborate as possible.
Is it possible to send for a pivotal study, not from the validation batches, but from a 100,000 tabs batch prepared in the R&D lab (with GMP accreditation)?
If yes, I guess that it is vital for the specifications of your batch to be the same as the ones from the validation batches (which have not been concluded yet).
What documentation is required in order to link the biobatch with the validation batches?

Thank you in advance,

Amalia

Complete thread:

UA Flag
Activity
 Admin contact
22,988 posts in 4,825 threads, 1,661 registered users;
122 visitors (0 registered, 122 guests [including 6 identified bots]).
Forum time: 21:08 CEST (Europe/Vienna)

The only way to comprehend what mathematicians mean by Infinity
is to contemplate the extent of human stupidity.    Voltaire

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