
Lisa S. Mazur
Articles
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1 month ago |
lexology.com | James Ravitz |Paul S. Gadiock |Marshall Jackson |Patrick Zanayed |Lisa S. Mazur |Jae Lee
On February 21, 2025, the US Food and Drug Administration (FDA) revised its shortage categorization of semaglutide, a glucagon-like peptide 1 (GLP-1) medication, marking the shortage as “resolved” for all presentations of the drug.
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Nov 19, 2024 |
mondaq.com | Lisa S. Mazur |Dale Van Demark |Amanda Enyeart |Marshall Jackson
The US Drug Enforcement Administration (DEA) further extended flexibilities that allow providers to prescribe controlled substances via telemedicine without first performing an in-person visit. The flexibilities were initially provided during the COVID-19 public health emergency (PHE) and were scheduled to expire on December 31, 2024. This extension extends the flexibilities through December 31, 2025.
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Oct 28, 2024 |
mondaq.com | Patrick Zanayed |Lisa S. Mazur |Marshall Jackson |Amanda Enyeart
MW McDermott Will & Emery More McDermott Will & Emery partners with leaders around the world to fuel missions, knock down barriers and shape markets. With more than 1,100 lawyers across several office locations worldwide, our team works seamlessly across practices, industries and geographies to deliver highly effective solutions that propel success.
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Oct 9, 2024 |
lexology.com | James Ravitz |Paul S. Gadiock |Marshall Jackson |Lisa S. Mazur |Patrick Zanayed |Paul Hughes | +1 more
On October 3, 2024, the US Food and Drug Administration (FDA) revised its shortage categorization of tirzepatide, a glucagon-like peptide 1 (GLP-1) medication, marking the shortage as “resolved” for all presentations of the drug. An end to the shortage has important implications for industry stakeholders at various points in the medication’s supply chain. Compounding pharmacies and providers should be aware of the impact this change in shortage status has on their operations.
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Sep 30, 2024 |
mondaq.com | Caroline Reignley |Marshall Jackson |James Cannatti III |Lisa S. Mazur
On September 24, 2024, the Office of Inspector General (OIG) at the US Department of Health and Human Services issued a report recommending additional oversight of remote physiologic monitoring (RPM) services furnished to Medicare beneficiaries. The full report is available here. Many of the issues highlighted by OIG are inherent to the current RPM codes established by the American Medical Association (AMA) but may not actually be problematic.
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