A vast majority of the current industry deficiencies which have led to isolated 483s, Warning Letters and Consent Decrees are the result of deficient technical documentation of the production processes for both injectables, devices and solid dosages.
Batch Production Record and Device History Record Review and Quality Assessment - Webinar By GlobalCompliancePanel
4 April 2013, Fremont, United States
Introduction
Venue
Online Training
Livermore Common, Online Training, California, Fremont, 94539, United States
Useful links
Organised by
GlobalCompliancePanel
Contact information
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
21st RSC Nucleic Acids Forum 鈥� 2025
11 July 2025 10:00-18:00, London, United Kingdom
Search
Advertisement
Spotlight
Explore
Membership
