Login

Continuous thermal validation

Eliminate re-validations. Ensure constant compliance. Reduce costs.

Struggling to meet urgent validation deadlines, manage quality across locations, or allocate resources for mapping studies? Minimize disruptive re-mappings and make sure that your entire operation continuously meets GxP temperature compliance requirements with Eupry’s Continuous Validation Solution.

  • Reduced compliance costs
  • Fewer interruptions, lower workload
  • Central quality control of all facilities

One solution keeping your operation – continuously – compliant

Eupry’s Continuous Validation Solution covers all your thermal validation, monitoring, and calibration requirements – in less time and at a lower cost.

The solution provides:

  1. Constant compliance: The setup consistently provides data sufficient to cover both validation and monitoring requirements of GxP.
  2. No more re-mapping: This eliminates the need to conduct – and keep track of – re-validations.
  3. Central quality visibility: With the online platform, you can easily monitor quality across all your facilities, units, and departments.

In other words, your operation is – and remains – compliant.

No more (keeping track of) re-mappings

Eupry’s Continuous Validation Solution eliminates the need for re-validation (unless the operation changes), meaning you no longer need to worry about keeping up with validation schedules across sites.

One validation – and you are done!

  • No re-mappings

  • No unnoticed quality risks

  • No hunting for information

  • No critical validation needs

The components of Eupry’s continuous validation solution

Tailored risk assessment

Continuous validation is built on a risk-based approach. Therefore, it begins with a risk assessment conducted by our validation team, which lays the foundation for designing a solution for your operation and provides documentation for auditors to prove that all requirements are being met.

Wireless data loggers

With the wireless Eupry data loggers, you have all the information you need at your fingertips. The loggers automatically transfer data to the software and send instant alerts in case of deviations – also, calibration is included.

Temperature compliance platform

The included platform gathers all documentation, providing an overview of validation results, monitoring records, and calibration certificates. It is easy to use (also for teams outside the quality field) and lets you monitor compliance from any screen, automate tasks, tailor deviation alerts, design validations, analyze data, and generate audit reports in seconds.

Specialized support

Temperature compliance is what we do. With hundreds of validations and monitoring setups under our belt, we are on top of the requirements of GxP to make sure you become – and stay – compliant. Our team tailors a setup for you, and we are always just a call away when you need us.

Add-ons (if you need them)

  • Mapping services: On-site, remote, or DIY mapping options tailored to meet GxP standards.
  • Centralized quality dashboard: One dashboard that gives a complete overview of compliance for all locations.
  • Standardized processes: Our team can help turn your requirements into actionable SOPs to harmonize procedures – and compliance – in your operation.
  • Reduced costs

    Trim costs by over 30% and reduce your compliance workload by minimizing validation work and automating cumbersome, manual tasks.

  • Constant compliance

    Guarantee continuous compliance across the entire operation. Never worry about validation deadlines, unnoticed compliance issues, or audit surprises again.

  • Fewer disruptions, smaller workload

    Reduce the burden on local teams with way (!) fewer validation interruptions, standardized procedures, and a digital solution, automating tasks.

  • Quality as a competitive edge

    Showcase top-tier quality standards to clients. Temperature compliance will no longer stand in the way of – but support – your business growth.

One vendor, one solution

All you need for thermal compliance

Minimize the amount of suppliers in your life. Eupry’s Continuous Validation Solution covers both validation, monitoring, and calibration. In other words, you are all set for all your temperature compliance needs – one platform, one vendor.

Better data, full visibility, total quality control

Integrating monitoring, mapping, and calibration in one digital platform creates better data than ever. Get the insights you need to gain full control of quality across your operation.

A digital overview of the compliance level of all sites means no need to travel or dig through piles of documentation.

  • Make sure that all sites continuously meet your requirements
  • Conduct trend analysis and compare KPIs across facilities
  • Mitigate risks before they evolve and make proactive improvements

Complete compliance confidence

Minimize the risk of non-compliance by making sure your operation consistently meets validation requirements. Also, our digital compliance solutions, of course, check all the requirement boxes of GxP:

  • FDA 21 CFR Part 11 module
  • ISO 17025-accredited calibration
  • ISO 9001-certified quality management
  • High compliance rating by, among others, Novo Nordisk
  • Fully IT and hardware-validated

Minimized friction when scaling your business

New locations? New product types? With quickly deployable validation services, extensive sensor options, wireless data loggers, and a cloud-based system, expanding your operation is just a call away.

Frequently asked questions about continuous validation

What is continuous validation?

Continuous validation is a systematic approach designed to maintain compliance and quality in GxP-regulated industries, such as pharma, biotech, and logistics, without the need for re-mapping. Unlike traditional methods, which often require extensive manual work to periodically re-map equipment and environments, continuous validation includes comprehensive data collection that covers monitoring and validation requirements continuously, making re-validation unnecessary unless the operation is changed.

Also read: Continuous validation: A framework to eliminate re-mapping

Why choose continuous validation?

Pharma, logistics, and other life sciences industries face strict regulatory demands, often complicated by:

  • Multiple facilities with varying quality management standards.
  • A lack of centralized visibility into compliance.
  • Re-validations being time-consuming and costly. Eupry’s continuous validation solution simplifies these challenges by giving you the tools to reach and maintain GxP-level temperature compliance at all locations.
Isn’t it more expensive since it uses more loggers?

Continuous validation requires more data loggers than traditional ongoing monitoring – so isn’t it MORE expensive? The short answer is no.

Not only does Eupry’s continuous validation solution remove stress about keeping up with re-validation schedules – and who can put a price on peace of mind – it is also often the more cost-effective solution due to the reduction of resources spent on re-validation.

Download our product catalog

Get an overview of how Eupry’s products can help with automating temperature compliance: monitoring, calibration and mapping of temperatures, humidity, CO2 and diff. pressure.

Initializing ...

Get started now

Minimize disruptive re-validations, ensure constant compliance, and reduce costs with Eupry’s Continuous Validation Solution.

Contact us

Have a talk with one of our (very nice) specialists to discuss your compliance needs and find the right solution for you.

Get in touch

Download a catalog

Explore the solutions for yourself first in our product catalog.

Get a free catalog