2025 Europe Tour
Compliance in GxP is changing, and our European Enterprise Team is going on tour to host a range of informal work sessions, sharing insights on the current and future state of thermal compliance – no pitches (promise), just practical insights and honest feedback.
Sounds relevant? Apply for a visit now.
- Insights into the current regulatory landscape + what's ahead
- Free gap assessment of your thermal compliance processes
- Good conversation with our specialists (and good food)
Apply for a visit or simply to hear more about the sessions. No strings attached.
What and why
From November 24th to December 5th 2025*, Eupry’s European Enterprise team is touring Europe to host informal meetings and work sessions with quality, operations, and automation leaders from the life science and pharma-logistics industry.
The meetings will be focused on your reality and compliance strategy, and give concrete takeaways you can use immediately when building or improving your compliance roadmap.
- The goal: Discuss your compliance roadmap and explore how top companies are evolving their GxP compliance strategies across multiple sites and borders.
- The format: 1-hour working session followed by an informal dinner or lunch, where we can continue the discussion in a more informal setting.
- The how: You apply, we have a talk, and if it is a fit we schedule a date and time for the visit.
- Do you want to join, but the dates don’t fit? Fear not, we might be able to accommodate or set something up at a different time, so reach out anyway.
Request a visit – or get more info
Fill out the form and we will get back to you to confirm it is a match – we want to make sure the conversation is actually useful for you.
What you will get
- Current trends + what's ahead: How top companies approach digital validation and compliance automation, and what shifts to expect in the near future.
- Gap scan: Quick review of your monitoring, calibration, alarms, and validation lifecycle with concrete improvement recommendations.
- Post-session memo: A 1-page summary of quick wins and a pilot checklist you can use immediately.
And, of course, lunch or dinner on us.
Who should join?
The sessions are designed for quality, operations, or automation leaders at pharma or healthcare logistics companies who:
- Operate under GMP or GDP standards
- Manage multiple sites across countries
- Want to improve compliance scalability and automation
If that is you then let's talk.
How does it work?
- You apply through the formula below
- We get back to you as soon as possible
- We have a 15-minute call to see if this makes sense for your team
- If it is a fit, we schedule a time and date for the visit
Who is Eupry?
Changing how GxP handles temperature compliance
At Eupry, we specialize temperature compliance for the world's most regulated industries – from pharma to healthcare logistics and biotech – by bringing validation, monitoring and calibration into one digital, GxP-compliant solution.
We serve 500+ customers across 50+ countries – from global pharmaceutical manufacturers to healthcare logistics leaders.
