How to harmonize temperature validation (and mapping)

in GDP and GMP

In a perfect world, your validation processes should not look different across sites, facilities, or mapping studies – but how do you idesign and implement one harmonized framework that lives up to GDP and GMP requirements and does not slow down your operation?

More efficient processes = no duplicate work, lowered costs
Standardized ways of working = minimized risks, higher quality levels

Lack of local staff time, uncertainty about compliance, and inconsistent validation and mapping processes across sites.

Sound familiar?

Validation is a regulatory must in GxP, but whether you are running a single facility or a global network, it can become fragmented, inconsistent, and expensive. The result is often duplicate work, delayed operations, and increased audit risk.

But not anymore!

What you will learn

In this webinar, we will show how to standardize your temperature validation practices.

We will cover the essentials of a scalable approach that ties corporate policy (ICH Q10) to local execution (GDP/USP/WHO/ISPE). You will see how to align mapping protocols, monitoring practices, and re-mapping triggers into one framework that fits single sites and scales across multiple facilities, countries, and even 3PL partners.

Key takeaways

How to conduct GDP/GMP-compliant thermal validation and create a standardized mapping strategy = ensure your (existing or new) facilities live up to pharma requirements.
Best practices for establishing harmonized compliance processes across multiple facilities, balancing central governance with site-level flexibility = no more worries about varying quality.
Practical steps to harmonize mapping protocols under GxP, WHO, and ISPE = align your working methods and gain full control of compliance.

Who is the webinar for

Whether you are running one warehouse or managing global quality across dozens of sites, this session will help you build a validation framework that is consistent, audit-ready, and efficient.

Why attend

Get actionable guidance for harmonizing mapping and validation protocols that reduce re-work and audit risks – whether at one site or many. Learn how to roll out a scalable, inspection-ready framework across multiple countries, sites, and partners. Save resources, speed up site readiness, and build confidence that your validation meets GDP and GMP everywhere.

The speakers

Jakob Konradsen, Chief Quality Officer, Eupry: Jakob is a co-founder of Eupry and leads its quality and compliance strategy. With deep expertise in GxP validation, he has guided hundreds of companies in harmonizing temperature compliance across facilities and global operations.
Anders Buchmann, VP Commercial, Eupry: Anders works closely with pharma and logistics companies worldwide to optimize validation and compliance processes. He brings real-world insight from these organizations and the operational impact of standardizing validation frameworks across sites.