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

• Further event details More information about the event

Speakers

• Bruce Davis, Senior Consultant, Engineering, QbD & Qualification Bruce Davis Global Consulting, United Kingdom

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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

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