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” (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 “How to Develop a Master Validation Plan”
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
Related events
8th International Conference on Nanomaterials Science and Mechanical Engineering
7 July 2026 08:00 - 10 July 2026 18:00, Aveiro, Portugal
The 59th Annual International Meeting of the ESR Spectroscopy Group of the 91AV
13 April 2026 15:00 - 16 April 2026 23:00, Colchester, United Kingdom
6th International Conference on Emerging Advanced Nanomaterials
16 November 2026 08:00 - 20 November 2026 18:00, Newcastle, Australia
Chemical Biology meets Drug Discovery
14 September 2026 09:30 - 15 September 2026 16:30, Cambridge, United Kingdom
Search
Advertisement
Spotlight
Explore
Membership
