Hi! We're CIM.AS! When you reach the bottom of this page, you'll know why we're so set on ridding pharma of the manual processes and paper stacks that are weighing it down - and why we think we're the best at doing that.
Patient safety is at the heart of pharma. But the GxP processes that ensure this are complex and time-consuming. They create tension between production and QA teams. And they disrupt production plans.
In fact, 30% of staff time is spent on documentation-related activities and the biggest delay in batch releases is related to the QA function.
Legacy systems not built for the digital age force production and QA teams to spend their time on manual documentation and chasing information across endless systems and files. All while they miss output targets and live in a constant fear of making mistakes.
That's what we're here to change.
Our customers come from a wide range of areas. But with decades of pharma experience, we are the ideal partner for:
Our quality and environmental management system is certified by Bureau Veritas according to ISO 9001 and 14001 and in 2025 we also achieved the ISO 27001 certification — the internationally recognized standard for information security management systems (ISMS).
The QEMS integrates best practices for project execution and environmental responsibility and allows us to standardize our processes and improve performance over time.
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CIM joined XANO Industri A/B in 2021.
XANO makes long-term investments in unique companies with growth potential, and we're grateful to be backed by such a strong owner.
About XANO:
Contact CEO Michel Seidelin for more information
