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Data Integrity in Quality Systems & Automated Technology
Date
September 23, 2020
Data Integrity in Quality Systems & Automated Technology | Data Integrity is a global issue and currently a major concern with FDA and MHRA and all leading regulatory agencies. Multiple FDA warning letters, MHRA and EU GMP non-compliance reports have highlighted major data integrity failures and data falsification in companies globally. The agencies guidance for data governance has expectations for records in both paper and electronic form and with industry moving towards automation processes, there is a clear need for firms and responsible employees to understand the issues around data integrity and how to build robust systems in both QMS and automation systems.
CASE STUDY 3: Critical Review of Quality and Manufacturing Data | Emer-Pen is part of General-Pharma’s auto-injector portfolio. It is a single-use drug-device combination product, comprising device components with sterile injectable solution cartridge…
Creating Comprehensive Responses To Regulatory Actions | With an increasing number of non-conformances, warning letters/OAIs for sites governed by US regulations, one has to ask what the missing link might be…