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

posted by raghavendra_s – 2010-06-21 12:02 (5836 d 06:31 ago) – Posting: # 5545
Views: 9,742

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:

UA Flag
Activity
 Admin contact
23,653 posts in 4,991 threads, 1,570 registered users;
113 visitors (0 registered, 113 guests [including 22 identified bots]).
Forum time: 18:33 CEST (Europe/Vienna)

To propose that poor design can be corrected by subtle analysis techniques
is contrary to good scientific thinking.    Stuart J. Pocock

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