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Getinge Selects Anaqua to Provide Single, Centralized IP Management Platform

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Anaqua, the leading innovation and intellectual property (IP) management technology provider announced that global medical technology company Getinge has selected Anaquaโ€™s AQX in order to consolidate the management of all its IP assets onto a single, centralized platform.

Founded in Sweden in 1904, Getinge provides hospitals and life science institutions in 133 countries with products and solutions that aim to improve clinical results and optimize workflows.

Anna Maria Lagerqvist Gahm,ย Head of IP & Digital Law at Getinge, said:ย โ€œWith our extensive range of products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing, life science and digital healthcare solutions and our strong international presence with operations in more than 40 countries worldwide, it was important to be able to improve the efficiency and coordination of our IP management by consolidating onto a centralized platform. AQX enables us to do that, while also providing highly integrated functionality in key areas such as analytics and invention management.โ€

Bob Romeo, CEO of Anaqua, said:ย โ€œGetinge focuses on helping its customers save lives through the products and solutions it develops, and on achieving its goal of becoming the worldโ€™s most trusted and respected medtech company. We are delighted to be supporting Getinge on that journey by helping manage and protect the companyโ€™s valuable IP assets. Anaqua continues to invest in offerings to meet and exceed the ever-evolving demands of the worldโ€™s most innovative life science companies.โ€

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Achieving absolute precision in pharmaceutical manufacturing necessitates a comprehensive and rigorous oversight of physical attributes, with color serving as a primary indicator of chemical stability and composition. By integrating sophisticated instrumentation into the laboratory environment, manufacturers can transition from subjective visual assessments to standardized, data-driven methodologies that satisfy the most stringent global regulatory requirements. This strategic focus on color measurement pharma QC facilitates the early identification of raw material impurities and ensures uncompromising batch-to-batch consistency in final dosage forms, thereby bolstering patient safety and brand reputation.

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