Nebraska Gov. Jim Pillen, Nebraska’s governor, signed an emergency regulation on June 29, regulating a medical marijuana marketplace after two legalizations. Measures to be taken In the election of November 2024, more than two thirds (67%) of voters backed it.
The following is an explanation of what you should do. Measure 438State regulators now have until October 2025 to award business licenses. They had to do this by July 1, in order to create a framework for the Nebraska Medical Cannabis Commission.
NMCC approved the emergency regulations during its June 26th meeting in Omaha. They were then sent to Pillen. It was necessary for the NMCC to adopt emergency rules before they could accept and review applications by aspiring entrepreneurs who wanted to dispense, manufacture, grow or transport medical marijuana.
A separate voter-approved Measures to be taken By legalizing a maximum of 5 ounces (or less) of medical marijuana for people with a doctor’s written recommendation, medical cannabis users and caregivers are protected from criminal prosecution. However, a licensed market will provide these patients with products which are thoroughly tested to ensure public safety and health.
Monico Oldenburg, Chairperson of the NMCC in a 26th June letter to Pillen wrote: “Failure would force Nebraskans from seeking out medical cannabis products or other similar products that are unregulated and could be harmful.” The inability of Nebraskans to get medical cannabis at a Nebraska-regulated establishment is detrimental to their health, safety and welfare.
The emergency regulations will expire at the end of September. In the next few weeks, the Commission plans to begin a formal process to create permanent rules. The NMCC will accept public comments until July 15 on emergency regulations. They can also submit their feedback. [email protected].
During its June 26th meeting, the NMCC signed an agreement with Governor’s Policy and Research Office and Nebraska Department of Health and Human Services to provide the Commissioners with administrative and legal services throughout the formal rulemaking processes.
Below is a list of all the emergency rulesVertical licensing is You can also check out our other blog posts. In each of the 11 states, only one dispensary licence can be issued. judicial districts. In five districts, there are 10 counties and more. Dispensaries, cultivation facilities, and manufacturing plants cannot be within 1,000 feet from schools, daycares, hospitals, or churches.
For a business or company to be eligible for licensing, it must have at least 51% of the ownership held by an individual who is either a Nebraska resident and/or a U.S. national. Licenses are not available for felons, or anyone who has committed a drug-related crime within the last 10 years.
The licenses cannot be transferred and they can only be renewed once every two years, as long as the cannabis business is still active.
In accordance with 2024 measures approved by voters, licensed businesses are not allowed to sell an amount that could result in qualified patients or caregivers possessing 5 ounces more cannabis.
Included in the list of products that are permitted under the Emergency Regulations:
- Tablets, capsules and tinctures for oral use;
- Lozenges or lozenges with a rectangular or square cuboid or cube shape.
- Gels, oils or creams;
- suppositories;
- The transdermal patch is a new type of product.
- Liquids or oils to be administered using a Nebulizer or Inhaler.
The proposed rules by the NMCC also ban raw plant matter, like flower, shatter, trim or pre-rolls or any product that is administered through combustion, smoking or vaping. The NMCC would ban any food or beverage that contains cannabis in the form of a baked product, a mixture or an infused ingredient.
Intoxicating products derived from hemp or cannabinoids like delta-8 THC, delta-10 THC, and other derivatives of the plant would also be banned.
Licensed dispensaries are required to keep records of daily inventory and sales invoices/receipts. Cultivators as well as manufacturers and transporters are required to keep the same records.
The packaging must be designed to protect the cannabis product from contamination. It should also include a tamper evident seal, an identification label that shows the manufacturer, their contact information or web address, as well as the date the product was manufactured and the expiry date. The labels must include these statements, in capital letters:
- List I Substances Controlled
- Children and pets should be kept away from the product.
- Only for medically qualified patients
- Intoxicating effects may take some time to occur.
- Please use extreme caution when using this product. It may affect your ability to drive or operate machines.
- The transfer of medical cannabis is against the law.
Patients and caregivers would be provided with a list of ingredients, batch/lot number, directions for consumption, amount of THC per dose, per container and unique registration and manufacturer numbers.
Emergency rules forbid packaging with cartoonish fictional characters, trademarks or trade dress that mimic or imitate products that are marketed primarily to minors or that include images of or likenesses or celebrities.
Under the proposed rule, either the commission or one of its employees could conduct on-site inspections without prior notice.
Two days after Lancaster County district judge Susan Strong A lawsuit was filed by John Kuehn, a former Republican State Senator who sought to stop the implementation of the measure approved by voters.
The Nebraska Attorney General Mike Hilgers has also threatened to file a lawsuit if the NMCC begins issuing licenses. Nebraska Examiner reported.
Nebraska Gov. Jim Pillen, Nebraska’s governor, signed an emergency regulation on June 29, regulating a medical marijuana marketplace after two legalizations. Measures to be taken In the election of November 2024, more than two thirds (67%) of voters supported this candidate.
The following is an explanation of what you should do. Measure 438State regulators now have until October 2025 to award business licenses. They had to do this by July 1, in order to create a framework for the Nebraska Medical Cannabis Commission.
After the commissioners’ meeting on June 26, in Omaha, approved these emergency rules, they were sent to Pillen. Before it could begin accepting applications and evaluating them, the commission had to have emergency regulations in place.
A separate voter-approved Measures to be taken Legalizing medical cannabis up to five ounces for patients with written recommendations from health practitioners protects them from prosecution and criminal charges. However, a licensed market will provide these patients with products which are thoroughly tested to ensure public safety and health.
Monico Oldenburg, Chairperson of the NMCC in a 26th June letter to Pillen wrote: “Failure would force Nebraskans from seeking out medical cannabis products or other similar products that are unregulated and could be harmful.” The inability of Nebraskans to get medical cannabis at a Nebraska-regulated establishment is detrimental to their health, safety and welfare.
The emergency regulations will expire at the end of September. In the next few weeks, the Commission plans to begin a formal process to create permanent rules. The NMCC will accept public comments until July 15 on emergency regulations. Industry participants and other interested parties may submit feedback through [email protected].
During the meeting on June 26, the NMCC also entered into an arrangement with the Governor’s Policy and Research Office and Nebraska Department of Health and Human Services. These agencies will provide legal and administrative support to the commissioners during the formal rules-making process.
Below is a list of all the emergency rulesVertical licensing is You can also check out our other blog posts. In each of the 11 states, only one dispensary licence can be issued. judicial districts. In five districts, there are 10 or more counties. The dispensaries as well as the cultivation and manufacturing facility cannot be placed within 1,000 feet or less of any schools, daycares churches, or hospitals.
For a business or company to be eligible for licensing, it must have at least 51% of the ownership held by an individual who is a U.S. Citizen and has lived in Nebraska for four previous years. Licenses are not available for felons, or anyone who has committed a drug-related crime within the last 10 years.
Licenses can be extended every 2 years, provided that the registered cannabis establishment is active.
In accordance with 2024 measures approved by voters, licensed businesses are not allowed to sell a quantity of cannabis which would allow a patient or caregiver who qualifies for cannabis use to possess more than five ounces.
Included in the list of products that are permitted under the Emergency Regulations:
- Tablets, capsules and tinctures for oral use;
- Non-sugarcoated cubes of gelatinous material, rectangular cuboids made from gelatinous material, or lozenges shaped like a cube, rectangular cuboid, or cube;
- Gels, oils or creams;
- suppositories;
- The transdermal patch is a new type of product.
- Fluids and oils that can be inhaled or nebulized.
The NMCC proposed regulations would prohibit the use of raw plant matter, like flower, shatter, trim or pre-rolls or any product that is administered through combustion, smoking or vaping. The NMCC would ban any food or beverage that contains cannabis in the form of a baked product, a mixture or an infused ingredient.
The intoxication of hemp products and cannabinoids, such as delta-8-THC or delta-10-THC would also be prohibited.
Licensed dispensaries are required to keep records of daily inventory and sales receipts. These must include the names of purchasers, the date and amount of the sale, the item sold, the price, the quantity and type of the product, the name and address of the buyer, the purchase and delivery dates, the items purchased, the costs, etc. Cultivators as well as manufacturers and transporters are required to keep the same records.
Packaging for cannabis must include the following: a seal that protects the product against contamination; a label with the licensee’s contact information or website, the date the product was manufactured, and the expiration date. The labels must include these statements, in capital letters:
- List I Substances Controlled
- Children and pets should be kept away from the product.
- Only for medically qualified patients
- Intoxicating effects may take some time to occur.
- Use extreme caution if you plan to operate or drive machinery after using this product.
- The transfer of medical cannabis is against the law.
The dispensaries are also responsible for giving patients and caregivers the following information: a complete list of the ingredients of a particular product, its batch number or lot, dosage instructions, milligrams of THC for each dose and container, as well as the manufacturer’s unique license and registration number.
These emergency regulations prohibit the use of packaging which depicts cartoon like fictional characters or contains symbols, logos and trademarks that are similar to or copy products marketed mostly towards minors. They also forbid images or likenesses that feature celebrities.
Under the proposed rule, either the commission or one of its employees could conduct on-site inspections without prior notice.
Two days after Lancaster County district judge Susan Strong A lawsuit was filed by John Kuehn, a former Republican State Senator who sought to stop the implementation of the measure approved by voters.
The Nebraska Attorney General Mike Hilgers has also threatened to file a lawsuit if the NMCC begins issuing licenses. Nebraska Examiner reported.
Cannabis Law Resources for Poland
Discover essential legal information about the cultivation of cannabis, its sale, and regulations governing medical products in Poland. You can use these resources to learn about the requirements for certifications, permissions and compliance.
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Polish News Registration and Interests of Cannabis Businesses
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Permissions for Cannabis Sales in Poland
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Authorization for Importing or Manufacturing Medical Products
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Permission for Manufacturing or Importing Medical Products
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Certificate of Good Manufacturing Practices (GMP)
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Registration of Medical Products in Poland