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PharmaRolly’s “best harvest yet” rooted in genetics, patience, and a cooperative summer

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9 months ago

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For Phrarolly, a producer of Medical Cannabis based in 2025 has been delivered by Stephen Malloy Call for its best harvest so far. “It is the result of the group’s years, deliberately minor changes, careful genetic selection and the weather worked for our side,” he noted.

From Humboldt County North Macedonia
The company has its source of genetics in the north of Humboldt Seed Company, California. “Humboldt climatic conditions of the mirror has been Northern Macedonia and long climates. We have been hunting for years, and he chose the best,” he explains. Than than to continue with high profile names, Farmarolly has been based on voltages that work well in the microclimate and the effects of consumers have been attractive, smells and flavors.

Stephen says that the season began with a cold march in decades, but the summer came to produce enough “happy plants” in the summer. “Some other European growing weather models mentioned profitability and quality challenge, our crop has arrived without harm.” The company grows in 400-liter fabric packaging filled with soils. This medium is more forgiveness than the inert media like Rockwool, Stephen explained. “The combinations of medium-sized plants are also stronger odor profiles.”

Post-harvest manipulation depends on quality. Pharmarolly’s drying room, after extensive research designed in 2020, allows tight moisture control before mining. “We didn’t go with the external system system,” Stephen says. “When you buy it from the box, you tell you what you mean, and you never think, we do what everyone else, we talk to experts and make decisions to build it because we want to take full responsibility for our processes.”

© pharmarolly

“The best harvest yet”
The current catalog of the company through a strange sativa pseudo-origin, with the Pines of Citrus Note, grape scent, garlic cream, tropical fruits and gassy pistachio profiles. They all grow in EU-GMP conditions, in Germany, in the UK and Switzerland require a strict microbiological compliance with export markets.

Phrantarolly also processes full distillation of full spectrum oil for exports, summaries like Rosin Live Rosin to consider for the future. Stephen sees the right model of its ecological cultivation, fresh frozen flowers can accelerate post-harvest periods and take care of the content of the terpenene.

Each lot suffers the full season with water, soil and product, heavy zero metals, low microbiology and high tereno and small cannabinoid content. “That’s the result of clean entries, strong genetics and environmental control. All have been the quality columns of this year.”

For more information:
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EU regulators say Charlotte’s Web hemp CBD safety “cannot be established”

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15 hours ago

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May 12, 2026

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The growing tension between international scientific findings and US health policy has raised questions about whether Medicare beneficiaries are being exposed to cannabinoid products whose safety profiles have not been fully established.

In March 2026, the European Food Safety Authority (EFSA) carried out a formal scientific evaluation of a shipment of Charlotte’s Web hemp product, concluding that the safety of a carbon dioxide extract derived from Cannabis sativa L. “cannot be established”. The agency identified several gaps in the available data, including significant portions of the product remaining uncharacterized, a lack of reliable toxicological studies on the actual material, a lack of human clinical data, and an unknown allergenicity and long-term safety profile.

At the same time, the Centers for Medicare and Medicaid Services (CMS) launched the Substance Access Beneficiary Engagement Incentive (BEI) program. The initiative allows participating healthcare providers to discuss and supply certain hemp and marijuana-derived cannabinoid products to Medicare beneficiaries under the authority of the Center for Innovation, and does not require approval from the US Food and Drug Administration. That distinction is at issue in a pending federal case: Smart Approaches to Marijuana (SAM), et al. Robert F. Kennedy Jr. et al., Case 1:26-cv-01081 (U.S. District Court for the District of Columbia).

Under the FDA’s standard framework, products intended for therapeutic use typically undergo controlled clinical trials, dose standardization, safety and toxicology evaluation, and manufacturing and stability validation. The BEI program operates outside of this structure. Some observers point out that this could introduce products into federally funded care settings before those benchmarks are met, while proponents of the program characterize it as a legitimate model of innovation.

Medicare beneficiaries represent a medically complex population, with many patients managing multiple medications, chronic conditions, and increased susceptibility to drug interactions. Cannabinoid compounds, including THC, interact with metabolic pathways such as CYP450 enzymes, which process many common medications. The safety profile of these products in this population has not been fully characterized through controlled studies.

Following the launch of the program, several companies publicly announced their positioning within the emerging healthcare supply chain. Charlotte’s Web highlighted alignment with CMS drivers and Cornbread Hemp announced institutional distribution through a national group buying organization, reflecting broader commercialization activity in the category.

SAM v. In Kennedy, the court is evaluating whether CMS overstepped its statutory authority by introducing avenues for the supply of cannabinoids without formal regulations, public notice and comment, or FDA validation standards. A resolution will determine whether the program is scaled back, modified, or stopped pending further review as implemented.

The EFSA’s conclusion does not ban the marketing of CBD products, but indicates that the scientific evidence necessary to fully establish their safety remains incomplete. The political debate reflects a broader question in health care regulation: how to balance the pace of innovation for therapeutic products with the standards of evidence typically required in federally funded systems of care.

Source: MMJ International Holdings

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Trump’s Medical Marijuana Move Focused On Helping Ailing Seniors, But Lack Of Coordination Could Cause Backlash (Op-Ed)

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15 hours ago

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May 12, 2026

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“The rush to provide medical marijuana to the elderly will require substantial legal, scientific, and commercial infrastructure, which in an ideal world would avoid repeating historical mistakes with clarity and coordination.”

By Emily Dufton

Everyone knows that the last month was historic for cannabis. There are big changes coming with the rescheduling of medical marijuana and federal Medicare coverage of hemp.

But what many have misunderstood is why.

For the first time in 56 years, a type of marijuana has finally escaped Schedule I of the Controlled Substances Act (CSA). Cannabis was placed there in 1970, and despite previous attempts at legalization – including 40 states that legalized medical access and 24 states that legalized recreational use – for more than half a century, cannabis continued to be defined as a substance with no approved medical use and a high potential for abuse.

Until last month, acting Attorney General Todd Blanche moved medical marijuana to Schedule III, a drug category with some medical uses approved and “moderate-low” addiction potential.

This review includes four cannabis products approved by the Food and Drug Administration (FDA) in all 40 states and Washington DC. These products are now Schedule III, which means that dispensary owners don’t have a heavy tax burden like 280E.

Medical marijuana became a much more legitimate industry.

But what makes this change even more historic is who it is intended to benefit: the elderly.

Previous legalization movements all focused on young adults. The decriminalization movement of the 1970s painted cannabis as an “adult right” for a mature baby boomer. Activists in the 1980s and 90s argued that medical marijuana was needed for young people struggling with HIV/AIDS. And in the 2010s and 2020s, social justice movements promoted legalization as a means to end the mass incarceration of Black youth.

Recriminalization movements have been equally concerned with pot’s impact on children. Reagan’s zero-tolerance, “Just Say No” drug war of the 1980s was launched explicitly to save children. And the intoxicating hemp products accidentally legalized in the 2018 Farm Bill are slated to be made illegal again this November, after opponents warned they sent too many children to emergency rooms.

But the Trump administration’s support for medical marijuana reform is based on something new: the concern of 18 percent of Americans over 65 — nearly 1 in 6 — a number expected to rise to nearly a quarter of the population by 2050.

A new industry is emerging to service this demographic. Howard Kessler, of the Commonwealth Project, is one of the biggest proponents of medical marijuana use for seniors.

A Project video (reposted by Trump on Truth Social last September) he seemed to be addressing the president directly. “You can revolutionize healthcare for the elderly,” begins the narrator, before listing cannabis’ positive effects on pain, stress and sleep. The video ends with the promise: “You will deliver the most important senior health initiative of the century, strengthening your legacy and transforming aging care. Millions everywhere will thank you.”

As a drug historian, I did not see this coming. The historic overhaul of medical marijuana is being hailed as a victory for the elderly, a demographic that was almost never included in the conversation.

For years, prohibitionists argued that today’s cannabis products are too strong, a far cry from the tamer, weaker weed of yesteryear. But with these new products aimed at seniors, this really is your grandma’s marijuana. The baby boomers who fought for decriminalization in the 1970s are getting it, in 2026, with federal funding from Dr. Mehmet Oz’s Centers for Medicare and Medicaid Services.

Focusing on the health and well-being of the elderly, Kessler’s campaign successfully overturned decades of drug policy concerns about children, and this shift will have major implications for both legalization and recriminalization campaigns. The “save the kids” attitude that changed the law before may not work when marijuana users are older.

But a backlash could arise just as quickly if unregulated “medical” products start harming grandma.

Therefore, as a historian, I am concerned that this project has been rapidly expanded with vocal support but little coordination. There is a significant lack of clarity on how this transformation will work.

Given that Schedule I marijuana has been around for half a century, the science behind medical cannabis is still a work in progress. It’s also not entirely clear who is responsible, as multiple entities are involved in the change, including the Drug Enforcement Administration, the FDA, the Department of Justice, and the Internal Revenue Service, as well as legislative, regulatory, and law enforcement agencies at the state and local levels.

And so far no one has addressed the impact it has had on hemp/marijuana distribution. Lack of coordination doomed previous legalization campaigns, and could harm reprogramming if it unfolds in a chaotic fashion.

At the moment, the outlook does not look promising. Dr. Gillian Schauer, executive director of the Cannabis Regulatory Association, told NPR, “We’re implementing policy that’s far from where the science is… It’s like flying an airplane blind when we’re building it without parts.”

Last month’s rescheduling was historic, but it’s also incomplete. The rush to provide medical marijuana to the elderly will require extensive legal, scientific and commercial infrastructure, which in an ideal world would avoid repeating historical mistakes by providing clarity and coordination.

It may not happen yet, but it’s what grandma deserves.

Emily Dufton is the author of Grass Roots: The Rise and Fall and Rise of Marijuana in America and Addiction, Inc.: Medication-Assisted Treatment and America’s Forgotten War on Drugs.

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Kambis expands cultivation infrastructure as Thai medical cannabis facility eyes international markets

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2 days ago

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May 11, 2026

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A certified medical cannabis facility in Thailand is adding a specialized mother room and an advanced drying room as part of its capacity expansion aimed at international supply.

KAMBIS Community Enterprise Innovative Farming announced through construction LinkedIndescribing the two rooms as nearing completion and central to the roadmap for scaling up production. The company sees investment as a prerequisite for consistent production in export markets, not just for increased volume.

The expansion is accompanied by an ongoing fulfillment push. KAMBIS has been working to prepare GACP and EU GMP, a combination that reflects the standard required to supply the regulated medical markets in Europe and elsewhere. The company noted that medical expertise has been embedded in its leadership since the beginning, and it says it has kept clinical requirements at the center of cultivation decisions as the operation has grown.

The addition of the mother’s room is particularly notable in the context of the international offer. The mother-room infrastructure allows the facility to maintain genetic consistency across production cycles, which is a prerequisite for the kind of batch-to-batch reproducibility required by EU GMP frameworks. Drying room capacity, on the other hand, is often the bottleneck that limits how many post-harvest flowers a grow site can fill without compromising quality metrics.

For more information:
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