Bioequivalence and Bioavailability Forum

Main page Policy/Terms of Use Abbreviations Latest Posts

 Log in |  Register |  Search

Back to the forum  2018-07-20 11:23 CEST (UTC+2h)

Guidance on document management system [GxP / QC / QA]

posted by raghavendra_s - 2010-06-21 10:02  - Posting: # 5545
Views: 4,095

Dear Madam/sir,

May I know if any specific regulatory guidances for industry are available on document management system/software apart from 21 CFR Part 11.

Thanks and regards,

Complete thread:

Back to the forum Activity
 Mix view
Bioequivalence and Bioavailability Forum |  Admin contact
18,547 posts in 3,941 threads, 1,192 registered users;
online 23 (2 registered, 21 guests [including 16 identified bots]).

If there is an exception to any rule,
and if it can be proved by observation,
that rule is wrong.    Richard Feynman

The BIOEQUIVALENCE / BIOAVAILABILITY FORUM is hosted by
BEBAC Ing. Helmut Schütz
HTML5 RSS Feed