Automated temperature mapping and monitoring
Best practices and mistakes to avoid
No more manual work. Is automation changing how we handle temperature mapping in GxP?
Digitization and automation are no longer optional in modern compliance processes.
The risks of siloed processes, information slipping through gaps, and manual errors can jeopardize both compliance and increase the likelihood of product spoilage.
As such, auditors increasingly expect to see digitalization of traditionally manual compliance processes.
By automating and digitalizing your temperature monitoring or mapping processes, you can streamline your operations, minimize resource waste, and ensure audit readiness.
However, in the world of compliance, where conventional processes are often favored, the move toward a digital-first way of working can seem both challenging and risk-filled.
How can you implement — or optimize — a digital temperature compliance operation that lets you standardize processes across (multiple) facilities while maintaining compliance?
Hear Jakob Konradsen, our Chief Quality Officer, and Aleš Ukmar, Senior Validation Specialist, share strategies and best practices for successful digitization of validation and monitoring practices across TCUs, facilities, and more.
Key takeaways
- Guidelines for digitalizing mapping and validation processes
- Key consideration when choosing a digital monitoring system
- The most common risks involved in automating temperature compliance
How to move from manual to digital mapping
Get a step-by-step roadmap for a smooth and secure shift from manual to digital processes.
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Client Testimonials
“I would absolutely recommend Eupry to other companies. I’m saving a lot of time (...) There is no travel involved and I can do the data collection and reporting remotely. Eupry’s program is the only one that I’ve found that can do that. This applies well to the US.”
Daniel Wassell
Equipment Validation Engineer
“The response times and availability from Eupry were very impressive. We have continuously been in contact with each other every step of the way. They helped us carry out various tests and assisted in the interpretation of the data – coming up with suggestions or feedback on whether the results were compatible with our requirements. It was undoubtedly a well-put partnership”
Joakim Sund
Quality Assurance Specialist at DSV Sweden
“I can do the data collection and reporting remotely. This applies well to the US.”
Daniel Wassell
Equipment Validation Engineer at Biocair US
