14:00 BST / 15:00 CET, Wednesday September 5, 2018

Ongoing software validation is a requirement of every serialization solution in the EU. With the FMD deadline fewer than 6 months away, pharma companies need to have a validation strategy that will ensure compliance from February 2019.

To understand the requirements and how to approach them, join us for an interactive webinar. This is an opportunity for everyone involved in the QA and compliance of your serialization solution to ask questions about:

• The GxP (good practice) standards that apply to serialization solutions.
• How to project manage your validation set-up.
• The impact of validation on your resources.
• Automating the validation process.

Speakers:

Our expert panel includes speakers from Epista Life Science, a leading consultancy in the field of validation:

• Hanne Harbo Hansen, Principal Consultant, Epista
• Emma Hagberg, Consultant and Project Manager, Epista
• Nick Daly, Senior Solution Consultant, TraceLink
• Allan Bowyer, Industry Marketing Director, TraceLink