CONTINUOUS temperature mapping = no more re-mapping
Is continuous mapping the game-changer in GxP? Watch the on-demand webinar to explore the framework, its use cases, pitfalls, and more.
- Reduce the total cost of ownership
- Fewer interruptions and a lower workload
- Heightened quality and central control (of all sites)
Step-by-step guidelines
... for continuous temperature mapping.
Practical examples
... of when the framework is – and is not – a good fit.
GDP and CEIV requirements
... and how continuous mapping aligns.
The speakers
Urgent validation needs, varying requirements, inconsistent processes, and missing quality resources.
Sound familiar?
The strict GDP requirements – often combined with multiple facilities with varying quality management, a lack of central visibility into compliance, and the fast pace of pharmaceutical logistics – can make it challenging to ensure that validation requirements are consistently met, leading to worries, bottlenecks, and unnecessary costs.
With continuous temperature mapping, you can make sure your operation continuously meets GDP and CEIV requirements for temperature compliance, without disruptive re-mapping studies.
In the webinar, Eupry co-founder and Chief Quality Officer, Jakob Konradsen, and VPC, Anders Buchmann, introduces the continuous mapping methodology, how to determine if it is a fit for your operation, and how to efficiently make sure your facility – or facilities – live up to GxP requirements.
Key takeaways
- The elements of continuous mapping and steps to implementing it in your operation.
- Practical examples of scenarios where the framework is – and is not – a good fit.
- How continuous mapping aligns with GDP, CEIV, and similar requirements.
- Guidelines for establishing a logistics operation that lives up to pharma requirements.
- Best practices for standardizing compliance processes across multiple sites.
