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    The FDA has granted 510(k) clearance to Werfen for its Aptiva Connective Tissue Disease Essential reagent to assist in the diagnosis of patients with autoimmune diseases, according to a manufacturer press release.This clearance complements Werfen’s previously cleared Aptiva Celiac Disease IgG reagent, and broadens the offerings of its Aptiva lab system, an automated, high-throughput system

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    • 📰The FDA has cleared @WerfenNA's newest reagent for #ConnectiveTissueDisease as the company sets its sights on expanding its offerings for other #autoimmune diseases How will this impact patient care? Read more 🔽 https://t.co/cS0MSNFhTr