4-6 June 2019 | Course | Manchester, UK
Equipment Qualification and Process Validation: ‘The Science- and Risk-Based Approach’
This highly participative three-day ‘master class’ is designed to ensure that you understand the current EU and FDA requirements for the design, execution, assessment and reporting of equipment qualification and process validation studies. The tutors are internationally recognised experts in the field and they will help you to be able to perform qualification and validation studies which meet the needs of the regulators in an efficient manner that will add real value to your business!
The course will explain how equipment/facility/utility qualification and process validation must link to patients’ needs and regulatory requirements, using tools such as risk management, statistical data analysis and change management to efficiently accomplish this. We will explain how to plan, design, execute and document qualification and validation activities to create an effective and efficient process that can add real value to your business and provide better protection to patients.
Event date: 4-6 June 2019
Event venue: Hilton Manchester Deansgate
Tel: +44 (0) 1751 432 999