Validating your cloud serialization solution

Live Webinar with Epista and TraceLink: Your questions, answered.

Ongoing software validation is a requirement of every serialization solution in the EU. With the FDM 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


Our expert panel includes speakers from Epista Life Science as well as TraceLink: 

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

Note that the event will take place at 14:00 BST / 15:00 CET, Wednesday, September 5th, 2018 

Learn more about the event and register here.