FDA Authorizes Expanded Use of Certain Noninvasive Patient Monitoring Devices
The FDA has authorized expanded use of some noninvasive patient monitoring devices to reduce contact between healthcare workers and patients.
Category: Industry & Regulatory News
Industry & Regulatory News
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Industry & Regulatory News
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Novalung ECMO Device Approved by FDA
The Novalung extracorporeal membrane oxygenation system is the first ECMO system to be cleared for more than six hours of use.
Industry & Regulatory News
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AARC Wants RTs to Earn a Bachelor’s Degree
"The time has come," said AARC President Frank Salvatore, for the respiratory therapy profession to advance it's education level, specifically by shifting to bachelor’s degrees.
Association News
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$100K Grant to Fund Research on COPD and Remote Monitoring
ResMed and the ATS Foundation have awarded a $100,000 Research Fellowship grant to advance the study of remote monitoring's role in helping to improve the management of patients with COPD.
Business News
LatestCF Foundation Supporting Development of Malabsorption Syndrome Therapy
The Cystic Fibrosis Foundation is supporting the development of Synspira's SNSP003, an orally-delivered non-porcine enzyme replacement therapy (ERT) designed to treat malabsorption syndromes.
FDA Approvals
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First Peanut Allergy Drug — Palforzia — Approved by FDA for Children 4-17
The US FDA has approved Palforzia to mitigate allergic reactions, including anaphylaxis, that may occur with accidental exposure to peanuts in children ages 4 through 17 years old.
Recalls & Advisories
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Teleflex Recalls Babi.Plus Pressure Relief Manifold Used for Bubble CPAP
Teleflex Inc has issued a recall for certain lots of the GaleMed Babi.Plus 12.5 cm H2O Pressure Relief Manifold, which is most commonly used for bubble CPAP therapy.