Russia BE Study [Regulatives / Guidelines]

posted by Helmut Homepage – Vienna, Austria, 2020-10-01 16:47 (199 d 08:05 ago) – Posting: # 21958
Views: 2,121

Hi Brus,

» Should the entire clinical trial be done in Russia or only the clinical part? I mean, can the bioanalytical part be done outside of Russia?

AFAIK, it can.

Dif-tor heh smusma 🖖
Helmut Schütz
[image]

The quality of responses received is directly proportional to the quality of the question asked. 🚮
Science Quotes

Complete thread:

Activity
 Admin contact
21,419 posts in 4,475 threads, 1,509 registered users;
online 7 (0 registered, 7 guests [including 2 identified bots]).
Forum time: Monday 00:53 CEST (Europe/Vienna)

There is one certainty in drug development
and statistics that one can depend on:
the data are always late.    Scott Patterson and Byron Jones

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