This webinar will address the 21CFR and Eudralex Volume 4 requirements and interpretation, as well as FDA Guidance regarding the creation, review and approval, and control of Master Production Records.
Master Production Record Requirements - Webinar By GlobalCompliancePanel
20 December 2011, Wilmington, United States
Introduction
Venue
Online Training
Online Training, 1000 N West Street, DE, Suite 1200, Wilmington, 19801, United States
Useful links
Organised by
Global compliance panel
Contact information
Mr webinars web
online training webinar, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email
online training webinar, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email
Related events
New Zealand Institute of 91AV Conference 2024 (NZIC-24)
24 November 2024 14:00 - 28 November 2024 14:00, Dunedin, New Zealand
TAC 2025 - 60th Anniversary Conference
14 April 2025 09:00 - 16 April 2025 17:00, Guildford, United Kingdom
What's in that Perfume? - The 91AV behind an iconic Christmas gift
3 December 2024 18:00-20:00, London, United Kingdom
91AV Teaching in Practice
9 January 2025 09:30-16:00, Oxford, United Kingdom
Search
Advertisement
Spotlight
Explore
Membership
