Fresenius Kabi’s Post

Another important step in plasma collection: The United States Food and Drug Administration (FDA) has granted 510(k) clearance to our Adaptive Nomogram, an alternate algorithm designed to optimize plasma collection efficiency with Aurora Xi Plasmapheresis System. This clearance enhances the capability of our Aurora Xi Plasmapheresis System, increasing plasma collection by an average of 11.6% per donation, while maintaining safety and effectiveness. We’re thrilled that this innovation will help plasma centers operate more efficiently and support a greater supply of plasma-derived therapies for patients in need. 👉 Read the full release here: https://lnkd.in/evGUugyQ #MedTech #FutureFresenius #CommittedToLife

  • Our image shows a plasma donation setting. A healthcare professional in a white lab coat and gloves is adjusting a medical device while a female donor reclines in a donation chair, her arm extended for the procedure. In the background, another donor is se
Dr JULIEN KOVHELE BEAVOGUI

Pharmacist, CEO, Founder & management director @ medicine Guinea sarl/ Pharma representation, regulatory, marketing, sales & consultancies/

2mo

Hi here as special scientist

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Ana Nascimento

Biomédica :Técnica de imunohemoterapia /Formadora/Criadora de conteúdos digitais sobre imunohemoterapia.

2mo

Amei

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Evelyn Hensen

senior Plasma Center technician 3 years at None

2mo

I'm looking for work 3 years at Bio Life spct

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Minh DK Nguyen

Assessor Pathology & CPR/AED First Aid Multidisciplinary Pathology - Data Manager Clinical Trials Research (Medical Oncology-Sir Charles Gairdner Hospital)

2mo

Yes, the concept is reasonable! This clearance is significant because it enables plasma centers to operate more efficiently, potentially increasing the supply of plasma-derived therapies, which are essential for patients needing treatments such as immunoglobulins, clotting factors, and albumin.?

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Así como lo ves contratan gente floja de papeles

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