Connect with us

Federal Policy

Medicare Coverage for Some Hemp-Derived Products Now Available

Published

on

Medicare Coverage for Some Hemp-Derived Products Now Available

Medicare’s pilot program covering hemp-derived products has officially launched. Under the plan, Medicare providers can be reimbursed up to $500 per patient each year for discussing and offering certain CBD products.

CBD products covered under the plan cannot exceed concentrations of 0.3% delta-9 THC, or more than 3 milligrams of THC per serving. Products must also be third-party tested and meet state and local standards. It excludes patients who have certain medical conditions, including substance use disorder and COPD.

In an April 1 statement, Centers for Medicare & Medicaid Services (CMS) Administrator Mehmet Oz said the agency “is committed to innovation that meets patients’ needs while maintaining strong safeguards and clinical oversight.”

“Under (President Donald Trump’s) leadership, we are expanding the tools available to improve patient health while generating important insights into how providers can use these tools safely and effectively in real-world care settings.” – Oz in one press release

CMS Innovation Center Director Abe Sutton added that “the initiative gives providers in certain models another tool — with necessary safeguards — to support their patients’ needs by consulting on whether the potential use of hemp products could help improve symptoms.”

The program is subject to ia suit brought by a coalition of health advocacy organizations and anti-cannabis groups that argues it violates the Social Security Act, which “does not permit CMS to sanction the possession and use of illegal and dangerous Schedule I substances by Medicare patients without express authorization from Congress.”

TG joined Ganjapreneur in 2014 as a news writer and began hosting the Ganjapreneur podcast in 2016. He is based in upstate New York, where he also teaches media at a local university.

Continue Reading

cannabis policy

Federal Bill Would Require Data Collection on Cannabis-Related Medicaid Spending

Published

on

By

Republican Congressman Plans to Reintroduce Bill to Reschedule Cannabis 

A federal bill introduced Monday would require the Secretary of Health and Human Services (HHS) to collect Medicaid spending on cannabis-related inpatient and outpatient care and emergency room visits related to cannabis use. The bill, sponsored by North Carolina Sen. Ted Budd (R), comes just weeks after launching a pilot program that allows Medicare providers to be reimbursed up to $500 per patient per year for discussing and providing certain hemp-derived cannabis products.

In a statement, Budd claims that the use of cannabis has “serious” health consequences and that lawmakers must “put the health and safety of the American people first, ban it completely.”

“This is exactly why lawmakers need access to reliable data detailing Medicaid spending related to marijuana abuse. Millions of Americans rely on Medicaid health care benefits, and my legislation will ensure that Congress understands the dangers of this drug and its impact on federally funded health programs.” – Stupid in a press release

The bill is supported by the anti-cannabis group Smart Approaches to Marijuana (SAM), which is also suing the federal government on the pilot program allowing reimbursement for hemp-derived products. In a statement, Kevin Sabet, CEO of SAM, said the organization “enthusiastically” supports the legislation.

“Senator Budd’s bill requires an accounting of taxpayer-funded health programs and the impact of normalizing this dangerous drug on their costs,” Sabet said in the statement, “and this is long overdue.”

In addition to collecting data on Medicaid costs related to cannabis use, the Marijuana Impact on Medicaid Act would require HHS to provide Congress with a report within one year of enactment that includes a summary of the findings from the data collection, in addition to making recommendations for possible legislative or administrative action to be considered.

TG joined Ganjapreneur in 2014 as a news writer and began hosting the Ganjapreneur podcast in 2016. He is based in upstate New York, where he also teaches media at a local university.

Continue Reading

DEA

Trump Administration Moves State-Licensed Medical Marijuana to Schedule III

Published

on

By

Trump Administration Moves State-Licensed Medical Marijuana to Schedule III

The Trump administration on Thursday moved FDA-approved marijuana products and cannabis products sold under qualifying state medical marijuana licenses from Schedule I to Schedule III under federal law, while also setting a new administrative hearing for June 29, 2026 to restart and expedite the broader DEA reprogramming process.

Department of Justice said The immediate action is intended to support medical research and state-regulated medical programs while maintaining “strict federal controls against illegal drug trafficking.”

For now, the change only affects FDA-approved marijuana products and state medical marijuana markets, not adult-use cannabis businesses. This distinction is critical for the broader industry: adult-use operators are not getting immediate 280E tax relief under this order, and the measure does not provide any direct bank relief for adult-use businesses that remain federally illegal.

The administration’s announcement also indicated that the existing rescheduling process initiated by the DEA under the Biden administration would be scrapped for a new, expedited process beginning with a hearing in June. That broader process is expected to determine whether marijuana in general will be moved out of Schedule I, a question that remains especially important to adult-use operators still mired in the federal-state standoff.

“After further review, the DEA is withdrawing the prior notice of HEARING and the completion of these proceedings to move more efficiently toward the completion of the full redefinition of marijuana. This action will expedite the administrative process, include established deadlines, and allow DEA to proceed in the most expeditious manner consistent with federal law. The DEA will hold a new administrative hearing beginning June 29, 2026, regarding the proposed rescheduling of marijuana. – through the announcement of the Department of Justice

While the change represents the most significant change in federal cannabis policy in decades, even if cannabis is fully reclassified as a Schedule III substance, people currently serving time in prison for possession of cannabis will not be directly affected by the change, and businesses on the adult-use side of the industry will still be considered federally illegal.

Continue Reading

cannabis policy

Anti-Cannabis Coalition Sues Trump Admin Over Medicare Hemp Coverage Plan

Published

on

By

Anti-Cannabis Coalition Sues Trump Admin Over Medicare Hemp Coverage Plan

A coalition of health advocacy organizations and anti-cannabis groups sued the Trump administration on Monday over its plan to allow Medicare coverage for hemp-derived CBD and THC products. Plaintiffs include Smart Approaches to Marijuana, Cannabis Industry Victims Educating Judges, North Carolinians Against Legalization of Marijuana, Cannabis Impact Prevention Coalition, LLC, Cannabis Industry Victims Seeking Justice, County Drug Foundation of America, Save Drugs Courses International Anti-Drug Alliance, Illinois Family Institute and North Carolina resident and SAM donor David Evans.

The lawsuit was filed after the Centers for Medicare & Medicaid Services (CMS) will begin covering CBD and THC products as an incentive to engage beneficiaries of substance access (BEI). The document names CMS Administrator Mehmet Oz and US Department of Health and Human Services (HHS) Secretary Robert F. Kennedy, Jr. as a defendant.

Under the proposed BEI, patients enrolled in certain federal health insurance programs could cover up to $500 worth of hemp-derived products each year. The lawsuit alleges that the plan violates administrative rules because the CBD and THC products covered by the program have not received Food and Drug Administration approval and because CMS did not publish a notice of proposed rulemaking, which prevented public comment.

The complaint further alleges that the program would violate the Social Security Act, which “does not permit CMS to sanction the possession and use of illegal and dangerous Schedule I substances by Medicare patients without express congressional authorization.”

“CMS’s action represents an unprecedented and unlawful assertion of binding decision-making authority that will profoundly affect the health of older Americans. “CMS took this action without the hurdles imposed by the administrative process, without any reasoned explanation, in violation of the agency’s final determination pursuant to the APA, and without statutory authority.” – Smart approaches to marijuana, etc. al v. HHS, US CMS

The filing alleges that Evans would be personally harmed by CMS’ changes because he is a Medicare recipient who was not allowed to submit public comment on the BEI and whose “health care relationship” with CMS is changed by the plan.

The lawsuit alleges that there is a “research gap” for medical cannabis and hemp products and alleges that “commercially available CBD products are contaminated and mislabeled.”

The suit seeks a temporary restraining order, a preliminary injunction, a stay of the agency’s action pending a judicial review, and asks the court to vacate the EIB, declare it illegal and permanently enjoin the policy.

Continue Reading
Advertisement

Trending

Copyright © 2021 The Art of MaryJane Media