Challenge
Traditional batch releases in the pharmaceutical industry heavily rely on costly and time-consuming destructive testing methods. The expenses associated with these approval processes can quickly escalate to thousands of euros per test, depending on the specific drug. Our mission is to introduce a paradigm shift by enabling releases based on product and production parameters, eliminating the need for destructive testing altogether. Join us in embracing a more efficient and cost-effective approach to batch releases without compromising on quality.
Solution
When seeking approval for an application device, we analyze the product and production data obtained from critical production runs to assess their predictability in relation to the quality of the end product. By leveraging advanced data analysis techniques, we provide insights that enable a more accurate evaluation of product quality during the approval process. Embrace our solution to enhance predictability and streamline the path to successful approvals for your application devices.
Results
Our comprehensive studies have empowered the pharmaceutical company to significantly reduce, and in some cases eliminate, the need for destructive testing. This breakthrough approach has led to remarkable cost savings, with testing and scrap costs slashed by up to 80%. Embrace our solution to unlock unparalleled efficiency and cost optimization in your pharmaceutical operations.
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