Our validation suite of courses is essential for you to keep up to date with the current expectations.
You can pick and choose to sign up for the training individually, or you can sign up for the full week depending on your requirements.
This highly participative three-day training course 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. Our tutors are internationally recognized 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!
This course will provide a concise, pragmatic approach to cleaning – it will provide you with an overview on how you can apply this to your own activities and assess your own process vulnerabilities. Using examples and applications from across the industry you will learn the correct approach whilst also formulating your own compliance plans to take forward.
Delegates will develop their knowledge and understanding of the topic by participating in a series of practical workshops and case studies. Taking risk-based approaches to computer system validation (CSV) as a starting point, subjects such as record and data integrity, agile development methodologies and validation of SaaS applications will be integrated into the workshop to reflect current ‘real-life’ issues about implementing and operating GxP compliant computerized systems.
Early bird and multiple delegate booking discounts available. Discounts also offered to NHS staff, regulators and charities – contact us for details.
Have a question or want to book a place? Register online or contact firstname.lastname@example.org