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
Amei
I'm looking for work 3 years at Bio Life spct
Well done
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.?
Congrats!
Así como lo ves contratan gente floja de papeles
Pharmacist, CEO, Founder & management director @ medicine Guinea sarl/ Pharma representation, regulatory, marketing, sales & consultancies/
2moHi here as special scientist