Every medical device company (OEM) must meet certain standards for validation of its transfer plans, facilities, clean rooms and processes. These standards apply for OEM's and suppliers to OEM's. This webinar on "How to Develop a Master Validation Plan鈥� (also known as Validation Master Plan) will provide a step-by-step procedure for all medical device companies and their suppliers that are in need of developing a plan for product/equipment transfer, facilities, processes or to develop a company standard.
Live webinar on 鈥淗ow to Develop a Master Validation Plan鈥�
11 March 2014, Houston, Texas,, United States
Introduction
Venue
Online
Online, 10777 Westheimer Suite 1100, Houston, Texas,, 77042, United States
Useful links
Organised by
Compliance2go
Contact information
Compliance2go
10777 Westheimer Suite 1100, Houston, Texas, 77042, United States of America
(877) 782-4696 , (832) 384-9698
Contact us by email
10777 Westheimer Suite 1100, Houston, Texas, 77042, United States of America
(877) 782-4696 , (832) 384-9698
Contact us by email
Related events
7th International Conference on Nanomaterials Science and Mechanical Engineering
8 July 2025 08:00 - 11 July 2025 18:00, Aveiro, Portugal
Drugging the Multimorbidity Associated with Ageing
17 January 2025 09:30-17:00, London, United Kingdom
Future Labs Live Basel
27 May 2025 09:00 - 28 May 2025 17:00, Basel, Switzerland
European Glycoscience Community Webinar Series
25 January 2024 15:00 - 19 December 2024 18:00
Search
Advertisement
Spotlight
Explore
Membership
