Typical Elements Required to be Included in the Batch Production Record and the Device History Record in order to Accomplish a Quality and Cost Effective Review and Quality Assessment based on current Regulatory Expectations.
Batch Production Record and Device History Record Review and Quality Assessment
13 August 2014, Houston, United Kingdom
Introduction
Venue
online
online, 10777 Westheimer Suite 1100, Houston, 77042, United Kingdom
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
Integrating chemistry, engineering and biology to create the next generation of vaccines
30 March 2026 10:00-18:00, Cambridge, United Kingdom
Chemical Biology meets Drug Discovery
14 September 2026 09:30 - 15 September 2026 16:30, Cambridge, United Kingdom
India Pharma Expo 2026
23 April 2026 09:00 - 25 April 2026 18:00, Hyderabad, India
Search
Advertisement
Spotlight
Explore
Membership
