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16 October 2019 09:00 - 17 October 2019 17:00, London, United Kingdom
Introduction
Course Overview
The two-day process validation in the US and EU, balancing science and risk during the product lifecycle meeting will help you gain an understanding of the EU and FDA process validation guidance, learn how to establish a process validation programme, under the link between Quality by Design and process validation as well as how to apply relevant tools for process validation including risk assessment.
Benefits of attending:
Know the scope of the FDA and EU validation guidelines
Establish a three-stage, science and risk-based, lifecycle process validation programme
Clarify similarities and differences between EU and US expectations
Understand how Quality by Design supports process validation
Realise significant business benefits from taking a science and risk-based approach
Useful links
Speakers
Bruce Davis, Senior Consultant, Engineering, QbD & Qualification Bruce Davis Global Consulting, United Kingdom
Venue
Rembrandt Hotel
Rembrandt Hotel, 11 Thurloe Place, London, SW7 2RS, United Kingdom
Contact information
Leigh White
Management Forum Ltd
10-12 Rivington Street
+442077494730
Contact us by email
