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FDA Authorizes First OTC Rapid Antigen Test for COVID-19

The Food and Drug Administration (FDA) has granted Emergency Use Authorization (EUA) to Ellume COVID-19 Home Test, the first over-the-counter (OTC) fully at-home diagnostic antigen test for coronavirus disease 2019 (COVID-19). The Ellume COVID-19 Home Test is a rapid, lateral flow antigen test developed with support from the National Institutes of Health’s Rapid Acceleration of…
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Prepare to E-Prescribe Controlled Substances

Beginning January 1, 2021, a federal law called the Every Prescription Conveyed Securely Act takes effect requiring that prescriptions for controlled substances covered under Medicare be prescribed electronically.
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Digital Health Tool Propeller Cleared for Use With Symbicort Inhaler

The Food and Drug Administration (FDA) has cleared the Propeller Health digital platform to connect with the Symbicort® Inhaler (budesonide, formoterol fumarate dihydrate; AstraZeneca), a corticosteroid and long-acting beta-2 agonist indicated for the treatment of asthma and COPD.  The Propeller platform includes a sensor that is attached to the inhaler. The sensor delivers insights on…