Standardize GDP temperature validation – and eliminate the need for re-mappings
Ensure continued GDP temperature compliance through the continuous validation framework – without the need for re-validation.
Register for the webinar now
Date: 25th of February, 2025
Time: 4.30 P.M. CET, 3.30 P.M. GMT, 9.30 A.M. CST
Understand the guidelines for GDP-compliant temperature validation and the continuous validation framework. Establish procedures that will let you ensure that all facilities always meet thermal validation requirements – without the need for costly, disruptive re-mappings.
Urgent validation needs, complex requirements, inconsistent quality processes and documentation across facilities, and missing local quality resources.
Sound familiar?
The strict GDP requirements – often combined with multiple facilities with varying quality management, a lack of visibility into the compliance of these sites, and the fast pace of the pharmaceutical logistics industry – can make it challenging to ensure that validation requirements are consistently met.
For quality teams, this will often lead to worries about compliance, bottlenecks, unnecessarily high costs, and time-consuming quality control and audits.
In this webinar, Eupry co-founder and Chief Quality Officer, Jakob Konradsen, and Validation Lead, Arsalan Bassir, will go through how to efficiently make sure your facility – or facilities – live up to GDP and CEIV requirements.
They will also introduce the “continuous validation” methodology, a framework that ensures that all your facilities continuously meet thermal validation requirements – without the need for costly, disruptive re-mappings.
Key takeaways
- Guidelines for conducting thermal validation and establishing a GDP-compliant operation = ensure your (existing or new) facilities live up to pharma requirements.
- Best practices for establishing harmonized thermal compliance processes across multiple facilities = no more worries about varying quality.
- The components of the “continuous validation” framework, how it eliminates the need for re-mappings, and how to implement it = reduce operational disruptions.
- Practical examples from real-life organizations = learn from others.
Why attend
Ensure GDP/CEIV compliance, free up local resources, and gain a competitive edge in the pharmaceutical market by ensuring that all facilities continuously meet thermal validation requirements.
- Ensure GDP/CEIV compliance: By ensuring continuous compliance.
- Centralized quality control: Gain visibility and control across all sites.
- Minimize disruptions: Keep your facilities operational without interruptions from re-validation.
- Free up local resources: Minimize the “quality burden” on local personnel.
- Build trust (and a competitive edge): Showcase top-tier quality levels to clients.
Meet the speakers
Arsalan Bassir,Validation Team Lead at Eupry
Jakob Konradsen,Co-founder & Chief Quality Officer at Eupry
Ensure reliable temperature validation for GxP – in less time
Perform GxP-compliant temperature validations in more efficiently, for fewer costs, and with full compliance confidence. Learn how in our mapping catalog.
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Client Testimonials
“The calibration of the Eupry temperature loggers is easy and quick. I received a box with the new sensors (…) It took me under an hour to calibrate 40 loggers – including the time it took to find the refrigerators.”
Kasper H. Christophersen
Research Associate at Novozymes
“Automated temperature monitoring allows us to relax knowing that the temperature is automatically recorded, giving us reliable alarms if temperature deviation occurs.”
Dora Adanic
Chief Operating Officer at Genera Research
“The Eupry data loggers were easy and convenient to set up, the flexibility of the system offers the possibility to be aware of any change whenever there is a problem, and more importantly, the archives which hold all data in the cloud can be achieved at all times.”
Elvis Bergue
Electromechanical and Water Manager at Axonova
