Illustration of Anvisa approving medical cannabis cultivation in Brazil, featuring scientists in a lab with plants and official documents.
AIによって生成された画像

Anvisa approves cannabis cultivation for medical purposes

AIによって生成された画像

The National Health Surveillance Agency (Anvisa) approved, on January 28, 2026, resolutions allowing cannabis cultivation for health treatments and research, along with new administration routes and plant imports. This step marks progress in the national production chain, easing access to plant-derived medicines. The changes broaden options for patients with severe illnesses while upholding strict restrictions.

On January 28, 2026, Anvisa's Board of Directors unanimously approved three resolutions regulating the cultivation, research, and production of cannabis by patient associations for pharmaceutical purposes. This decision updates RDC 327/2019 and marks a regulatory milestone in Brazil, where cultivation of Cannabis sativa—including hemp and marijuana—has been banned since Decree-Law No. 891 of 1938.

The new rules allow cultivation in controlled locations with THC levels below 0.3%, exclusively for medicinal and research use, including criteria like georeferenced coordinates and diversion prevention plans. Previously, pharmaceutical cultivation was prohibited, forcing imports of extracts and raising costs. In 2024, the Superior Court of Justice (STJ) authorized hemp planting for industrial and medicinal purposes, mandating Anvisa regulation.

Other changes include new administration routes—buccal, sublingual, and dermatological, in addition to prior oral and inhalation methods—and permission for compounding pharmacies to prepare pure cannabidiol phytopharmaceuticals. Plant imports are now allowed for national manufacturing, potentially lowering prices. Products exceeding 0.2% THC can be accessed by patients with severe debilitating diseases, not just terminal ones.

"It's an important milestone," says Bruno Pegoraro, president of the Ficus Institute, highlighting progress in the production chain. Physician Guilherme Nery from the Cannabis in Practice Institute praises the democratization and personalization of treatments. As of December 2025, there were 33 cannabidiol products and 16 cannabis extracts authorized in the country.

Despite the advances, the 0.3% THC limit is criticized as restrictive; Pegoraro advocates raising it to 1% for severe pain cases. Bill 299/2015, approved by a committee in 2021, remains stalled in Congress, underscoring legislative delays harming patients and the productive sector.

人々が言っていること

Reactions on X to Anvisa's approval of cannabis cultivation for medical purposes are predominantly positive, with politicians, journalists, and users praising it as a historic advancement for patient access, research, reduced import costs, and overcoming prejudice. Posts emphasize benefits for severe illnesses, SUS strengthening, and science over obscurantism. No significant negative or skeptical sentiments found in high-engagement discussions.

関連記事

Laboratory scene showing cannabis flower products with overstated THC labels next to accurate testing equipment and an audit report, illustrating Colorado's cannabis potency labeling issues.
AIによって生成された画像

コロラドの監査で多くの大麻花のTHCラベルが過大評価されていることが判明;濃縮物はほぼ正確

AIによるレポート AIによって生成された画像 事実確認済み

コロラド大学ボルダー校主導の州全体の分析で、コロラドで販売される大麻花製品の約43%が州の±15%精度閾値外のTHCレベルを記載しており—そのほとんどが効力を過大評価—一方、濃縮物の96%がラベルと一致したことがわかった。この結果は、消費者信頼を高めるためにより厳格なテストと明確なパッケージングの必要性を示唆している。

2,500件以上の研究の包括的分析は、医療用大麻が広範な有効性への公衆の広く信じられているにもかかわらず、わずかな特定の用途でのみ強い証拠があることを示す。UCLA Healthの研究者主導のレビューは、慢性疼痛や不安などの状態に対する認識と科学的証拠のギャップを強調し、特に青少年と日常使用者に対する潜在的リスクを特定する。

AIによるレポート

US President Donald Trump signed an executive order recommending the easing of federal marijuana regulations, a potentially significant shift in the country's drug policy. The measure directs the attorney general to advance reclassification of the drug, possibly moving it from Schedule I to Schedule III. The decision aims to boost medical research and could affect the cannabis industry, though marijuana would remain federally illegal.

テキサス生物医学研究所の研究によると、大麻の活性化合物であるTHCのマイクロドーズが、HIV治療の長期的な副作用を軽減し、陶酔を引き起こさないことが示された。リhesusザルでは、低用量THCが炎症を減少させ、セロトニン濃度を増加させ、有害なコレステロールと胆汁酸を低下させつつウイルス抑制を維持した。この知見は、HIV保有者の慢性合併症管理の可能性を示唆する。

AIによるレポート

Authorities in Huila department intercepted a truck carrying 910 kilograms of marijuana hidden in plastic rolls, bound for Bogotá. The driver was arrested after attempting to flee. The seizure is valued at over 600 million pesos.

Brazil's National Health Surveillance Agency (Anvisa) approved the drug lecanemabe, marketed as Leqembi, on Thursday, January 8, for patients with early-stage Alzheimer's. The monoclonal antibody, administered via infusion, slows disease progression in individuals with mild cognitive impairment and confirmed beta-amyloid protein in the brain. The approval marks progress, though it is not a cure.

AIによるレポート

Cuba reaffirmed its zero-tolerance stance on drugs at the CELAC-European Union bi-regional forum in Brussels. The island's Foreign Ministry reported this firm position.

 

 

 

このウェブサイトはCookieを使用します

サイトを改善するための分析にCookieを使用します。詳細については、プライバシーポリシーをお読みください。
拒否