Meet complex regulatory requirements and take new drugs and devices to the market quickly and efficiently with our suite of pre-validated pharma 4.0 software for vision inspection, digital compliance and data insights.
Pharma manufacturers are faced with a need to increase capacity to overcome drug shortages and meet the demands for new blockbuster drugs. At the same time, they must adapt production to handle smaller batches – right down to the batch of one – without driving up the cost.
But some common challenges stand in the way:
Our suite of standardized software solutions shortens batch changeover time and increases productivity in pharmaceutical fill-finish operations, while supporting 21 CFR part 11 compliance and continuous process improvement.
Read more about our pharma 4.0 software products below.
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Log critical GxP data automatically and have reliable data at hand for audits, non-conformity investigations, product release and process optimization.
Digital Compliance lets pharma say a long overdue goodbye to decentralized logging in each level 1 or 2 component and an abundance of paper forms.
Manual inspection between batches easily takes an hour for two trained operators. Our system for automated line clearance uses vision technology to support operators in their work, ensuring a high level of accuracy.
The CATCH.AI production data platform solves three major challenges in pharmaceutical manufacturing:
A quick glance at any pharma company’s sustainability report is enough to tell you that the industry is concerned about its impact and prepared to take action.
By prolonging equipment lifetime and increasing output, our solutions can contribute to reducing the need for building new sites and purchasing new equipment.
As they increase efficiency and help manage the use of resources, our solutions make it possible to scale and launch new drugs at a reasonable cost, securing patients all over the world the treatment they need.
Anders Meister, Chief Commercial Officer