Controlled Substances & Regulatory Practice

Joshua Bauchner and Kelsey Barber Present on New Jersey Marijuana Business Operations

Shareholder Joshua S. Bauchner and associate Kelsey M. Barber will present during the National Business Institute’s Marijuana Operations in New Jersey seminar. They will address critical human resources, labor, and employment issues affecting marijuana and cannabis businesses operating in New Jersey. Their session includes key considerations for hiring and training employees, navigating 401k issues specific to the industry, and understanding corporate governance. Bauchner and Barber also will provide an ethics presentation exploring rules of professional conduct, the duty to pursue justice, attorney use of cannabis, and attorney ownership of cannabis businesses.

The full-day seminar will be offered live online on August 21, 2023, and available to view on demand. Learn more and register for this information-packed program presented by cannabis industry leaders.

As one of the most rapidly evolving industries today, lawyers in the cannabis space must be educated on licensing, operations, and employment issues such as drug testing. Contact an attorney in our Controlled Substances and Regulatory Law Practice Group with any questions about this emerging area of law.

In Major Advancement, FDA Issues First-Ever Draft Guidance on Clinical Trials for Psychedelic Drugs

By Josh Bauchner

Maligned, stigmatized, and marginalized for decades, psychedelic drugs have long been off-limits for researchers and others who wanted to explore the potential therapeutic uses of these substances for various conditions, including PTSD, depression, substance abuse, and anxiety. Now, in a significant step that offers the promise of new medical treatments and advancements, the U.S. Food and Drug Administration (FDA) issued its first-ever guidance for those wishing to study and test psychedelics for medicinal use.

Released on June 23, 2023, the FDA’s draft guidance contains non-binding recommendations for designing clinical trials for psychedelic drugs. According to the FDA, the draft guidance aims to “advise researchers on study design and other considerations as they develop medications that contain psychedelics.” As used within the guidance, the term “psychedelics” refers to “‘classic psychedelics,’ typically understood to be drugs such as psilocybin and lysergic acid diethylamide (LSD) that act on the brain’s serotonin system, as well as ‘entactogens’ or ’empathogens’ such as methylenedioxymethamphetamine (MDMA).”

The guidance discusses basic considerations throughout the drug development lifecycle, including trial conduct, data collection, participant safety, and new drug application requirements. Emphasizing psychedelics’ potential for abuse and psychoactive effects such as hallucinations and mood and cognitive changes, the FDA notes that this creates “a drug safety issue that requires careful consideration and putting sufficient safety measures in place for preventing misuse throughout clinical development.” This includes addressing potential interactions with drugs like antidepressants or lithium and “the role of psychotherapy in psychedelic drug development, considerations for safety monitoring and the importance of characterizing dose-response and the durability of any treatment effect.”

Outlining the needed steps for psychedelic drug testing and study, the FDA provides recommendations for nonclinical safety and toxicology studies, with examples of when extensive previous trial data could substitute typical animal toxicology testing in trials under an Investigational New Drug Application (INDA). The guidance notes that since psychedelics are Schedule I controlled substances, activities associated with investigations under an INDA must comply with applicable Drug Enforcement Administration regulations.

The FDA released its guidance days after legislation was introduced in Congress with bipartisan support directing the agency to do so. While it is unclear what the guidance will look like in its final form after the 60-day public comment period, the legislative and regulatory movement to allow for more research and testing of psychedelics for therapeutic use is a positive development for individuals seeking relief from a wide range of debilitating conditions.

If you have questions or concerns about the FDA’s draft guidance, please contact an attorney in Ansell.Law’s Controlled Substances and Regulatory Law Practice Group.

Congratulations to Joshua S. Bauchner on His Achievements as the New Jersey State Bar Association’s Cannabis Law Committee Co-Chair

Ansell Grimm & Aaron, PC congratulates shareholder Joshua S. Bauchner on his many achievements as co-chair of the New Jersey State Bar Association’s Cannabis Law Committee. Along with co-chair Lisa A. Gora, a partner at Epstein Becker & Green, Joshua led the Committee in making significant advancements, including:

  • Hosting eight CLEs at the Law Center on a range of cannabis-related topics.
  • Hosting three CLE panels at the State Bar Convention.
  • Expanding the Committee to include psychedelics.
  • Preparing two Reports and Recommendations to the New Jersey Cannabis Regulatory Commission on its initial Rules and Regulations.

The Committee also laid the groundwork for new initiatives in the 2023-2024 term, including promoting expungements of cannabis-related convictions and developing guidelines for Workplace Impairment Recognition Experts (WIREs).

We commend Joshua Bauchner and Lisa Gora, and all of their colleagues on the Committee, and thank them for their leadership and commitment to the practice of controlled substance and regulatory law. You can read their letter to the Committee here.

The New Jersey State Bar Association’s Cannabis Law Committee was formed to bring together attorneys to examine the many legal issues that stem from the medicinal and adult-use access to cannabis.

As one of the most rapidly evolving industries today, lawyers in the cannabis space must be educated on licensing, operations, and employment issues such as drug testing. Contact an attorney in our Controlled Substances and Regulatory Law Practice Group with any questions about this emerging area of law.

New Jersey State Bar Association Cannabis Law Committee Announces New Initiatives

The New Jersey State Bar Association recently welcomed new co-chairs of its Cannabis Law Committee. The Committee also announced vital new initiatives related to the cannabis industry which are being pursued in the 2023-2024 term. The committee was previously co-chaired by Ansell Grimm & Aaron shareholder Joshua S. Bauchner and Epstein Becker & Green partner Lisa A. Gora. Bauchner and Gora chaired the Committee for two terms concluding on June 30, 2023.

The new initiatives, announced at the May NJSBA convention in Atlantic City, will promote expungements of cannabis-related convictions and develop guidance for Workplace Impairment Recognition Experts (WIREs). The new committee co-chairs also plan to support increased education at local bar associations. Bauchner, in his role as outgoing co-chair, is quoted in an article discussing these new appointments and initiatives. Read the article here.

As one of the most rapidly evolving industries today, lawyers in this space must be educated on licensing, operations, and employment issues such as drug testing. Contact an attorney in our Controlled Substances and Regulatory Law Practice Group with any questions in this emerging area of law.

Joshua S. Bauchner Named a NJ Cannabis Insider 2023 Award Finalist

Ansell Grimm & Aaron is pleased to announce that Joshua S. Bauchner is a finalist for the NJ Cannabis Insider 2023 Awards! He has been nominated in the Excellence in Cannabis Law: Employment Lawyer category.

Voting is now open and can be done once per day through May 8, 2023. Please join us in supporting Josh by submitting as many votes as possible for him. Click here to cast your vote.

As head of the Controlled Substances and Regulatory Law Practice Group, Josh co-hosted on behalf of the Firm the first-ever Cannabis Symposium in New Jersey which drew nearly a thousand people (two other Symposia followed). He is co-chair of the New Jersey State Bar Association Cannabis Law Committee, a member of the NORML Legal Committee and Amicus Committee, has spoken at the Cannabis World Congress and Business Expo at the Jacob Javits Center, and has presented CLE’s on cannabis at the NY and NJ State Bar Associations, among other fora across the country. He also was honored with the New Jersey Law Journal’s Innovator of the Year Award for his work in the cannabis space and also publishes regularly on the topic.

The attorneys in the group understand the complex laws related to the production, sale, use, regulation, and legalization of controlled substances, including hemp, cannabis, and psychedelics. A multifaceted area of the law with conflicting regulations from different governing bodies, we help our clients navigate all aspects of this emerging field. 

Ansell Grimm & Aaron Congratulates Clients for Securing Cannabis Licenses

Ansell Grimm & Aaron, PC is pleased to congratulate its latest clients to secure annual cannabis licenses from the Cannabis Regulatory Commission. The Social Leaf, LLC was awarded an Annual Class Five Retailer License, and CSDE Manufacturing, LLC was awarded an Annual Class One Cultivator License. The Commission issues licenses for medicinal and recreational cannabis business operations in New Jersey. We proudly support these developing businesses.

Our Controlled Substances and Regulatory Practice attorneys understand the complex laws related to the production, sale, use, regulation, and legalization of controlled substances, including hemp, cannabis, and psychedelics. A multifaceted area of the law with conflicting regulations from different governing bodies, we help our clients navigate all aspects of this emerging field. We are committed to helping our clients understand their rights and opportunities in this evolving area of law.

9th Circuit to Decide Whether the Federal Government Can Continue to Deprive End-of-Life Patients of Psilocybin’s Palliative Benefits

By Joshua S. Bauchner and Rahool Patel

Much ink has been spilled over the past decade about the absurdity of the federal government’s insistence on maintaining marijuana’s listing as a Schedule I drug with “no accepted medical use” under the Controlled Substances Act (CSA) despite ample evidence of and consensus about marijuana’s therapeutic and medical benefits. A similarly illogical and unjust prohibition against the therapeutic use of another drug – psilocybin – is the subject of a current challenge before the United States Court of Appeals for the 9th Circuit. The outcome of this pending litigation will determine whether the Drug Enforcement Administration (DEA) can continue to deprive countless palliative care and end-of-life patients of a therapy that can help them with unrelieved anxiety and depression in their remaining days.

The case, which has taken a long and winding path back to the appellate court, has attracted the interest and involvement of scores of clinicians, patient rights groups, and drug reform advocates. These parties have submitted amicus briefs to support the rescheduling of psilocybin so that dying patients can avail themselves of the relief the drug may provide. Among those groups is the National Organization for the Reform of Marijuana Laws (“NORML”), whose amicus brief was prepared and filed pro bono by Ansell Grimm & Aaron attorneys Joshua S. Bauchner and Rahool Patel.

“A Law Enforcement Agency Lacking Scientific and Medical Expertise Dictating the Outcomes of Drug Scheduling”

The efforts to reschedule psilocybin and the litigation that followed were commenced by Seattle-based physician Dr. Sunil Aggarwal, who asked the DEA to approve the use of the drug for his palliative care patients under the 2018 federal Right to Try (RTT) Act. That law allows certain patients access to investigational drugs outside of clinical trials.

Despite the fact that the Food and Drug Administration (FDA) had twice designated psilocybin as a “breakthrough therapy,” thus making it potentially eligible for use under the RTT, the DEA refused Aggarwal’s request. Aggarwal then asked the 9th Circuit in 2021 to order the DEA to allow him to treat his patients with psilocybin, arguing that the RTT superseded the CSA’s ban on the use of the drug. However, the court dismissed the petition on procedural grounds, as the DEA had not yet issued a final agency decision that would allow for judicial review.

After the dismissal, Aggarwal continued his fight but changed his approach. Instead of challenging the DEA’s decision under the RTT, he affirmatively petitioned the DEA in February 2022 to reschedule psilocybin as a Schedule II drug, which would allow for its therapeutic use.

The DEA was equally unmoved by this effort and summarily rejected Aggarwal’s petition in September 2022, asserting there was no scientific evidence that would justify rescheduling. The pending litigation ensued, in which Aggarwal is asking the 9th Circuit to vacate the DEA’s denial and remand the petition back to the agency on the grounds that the DEA did not follow the required procedure when denying the petition.

Specifically, Aggarwal asserts that the DEA violated the law by failing to consult the FDA to assess psilocybin’s potential uses. As noted, the FDA had previously designated it as “breakthrough therapy,” facilitating research into its potential medical applications. As Aggarwal asserts in his initial brief, “DEA disregarded procedures Congress established to cabin the agency’s authority and to prevent precisely what has happened here: a law enforcement agency lacking scientific and medical expertise dictating the outcomes of drug scheduling.”

The firm is proud to stand with Dr. Aggarwal and his efforts to make a promising and game-changing treatment available to ease the pain of patients nearing the end of their lives and others who may benefit from such therapies. The federal government’s imperviousness to scientific and medical evidence that does not align with their obsolete treatment of potentially beneficial drugs unjustly interferes with the doctor-patient relationship and deprives patients of much-needed relief.

CONTROLLED SUBSTANCES AND REGULATORY LAW DEPARTMENT UPDATE – FEBRUARY 2023

 

 

 

 

 

Ansell Files Amicus Curiae Brief In Support Of De-Scheduling Psilocybin

Ansell Grimm & Aaron, PC once again proudly joins the National Organization for the Reform of Marijuana Laws (“NORML”) in securing access for patients, especially veterans, to the scientifically established medicinal benefits of psilocybin. Americans waited a half-century before gaining access to medicinal cannabis while the federal government continues to pursue a racist agenda in the face of legalization in nearly 40 states. History must not repeat itself. The federal government must stop interfering in the doctor-patient relationship.

In furtherance of this objective, Firm attorneys Joshua S. Bauchner, head of the Controlled Substances and Regulatory Law Practice Group, and Rahool Patel served as the principal authors of a pro-bono amicus curiae brief on behalf of NORML in support of Petitioners in Dr. Sunil Aggarwal, MD, PhD; Advanced Integrative Medical Science Institute, PLLC v. U.S. Drug Enforcement Administration; Anne Milgram in Her Official Capacity as Administrator of the U.S. Drug Enforcement Administration; and Merrick Garland in His Official Capacity as Attorney General, No. 22-178, in the United States Court of Appeals for the Ninth Circuit.  A copy of the brief may be found here.

In summary, the brief cautions the federal government against allowing history to repeat itself, providing an historical account of NORML’s efforts to decriminalize cannabis for medicinal purposes for the past half-century and the never-ending efforts of the federal government to delay, resist, and obstruct the progress of science and medicine.  While the federal government is unlikely to learn any lessons from the past, NORML hopes that the Court will acknowledge and heed the legal and procedural lessons learned from those past administrative petition litigations so that innocent dying patients – who are the true victims of the government’s misbehavior – are not denied readily available medicine.

NORML’s mission is to move public opinion sufficiently to legalize the responsible use of marijuana by adults, and to serve as an advocate for consumers to assure they have access to high quality marijuana that is safe, convenient and affordable.

The Firm previously filed a pro-bono amicus brief in the United States Supreme Court in the matter of Washington v. Barr, on behalf of several non-profit organizations representing former national and international professional athletes in support of a constitutional challenge to the federal government’s continued refusal to remove marijuana from Schedule I of the Controlled Substances Act, even though millions of Americans use marijuana on a regular basis to manage debilitating health conditions in accordance with State, territorial, and local laws. Unfortunately, with the passing of Justice Ginsberg, petitioners were unable to secure the four votes necessary to secure review.

Ansell Celebrates Five-Year Anniversary of the New Jersey Cannabis Symposium

In honor of the first-ever New Jersey Cannabis Symposium, which was held on January 26, 2018, which recently celebrated its fifth anniversary, Ansell Grimm & Arron, PC is proud to acknowledge the many milestones of success and rapid growth and development, particularly with respect to licensure, since that fateful night. Many have since held meetings and events promoting cannabis decriminalization and legalization in the State, but none have replicated the energy and enthusiasm on display that night.

Nearly 1,000 people interested in taking a role in the legal adult use cannabis industry attended the NJ Cannabis Symposium at the New Jersey Performing Arts Center that night.  Media coverage of the event was extensive with reports appearing on New York’s NBC and ABC affiliates, on FIOS1 News, in NJBiz.com, and on NPR and Good Morning America.

As Ansell Partner Joshua S. Bauchner then told the Asbury Park Press, “The time is now. If you’re starting today or tomorrow, you need to ramp up. There’s a tremendous amount of work to be done before we get to the actual filing of the licenses – getting your team together, getting your capital, finding your space, figuring out your banking.” Bauchner, a featured speaker at the Symposium, leads Ansell’s Controlled Substances and Regulatory Law Practice Group which also co-hosted the Symposium alongside the BSC GroupLongview StrategicMarcum LLP, and the New Jersey Cannabusiness Association.

Since that time, including the passage of the New Jersey Cannabis Regulatory, Enforcement Assistance, and Marketplace Modernization Act (“CREAMMA”), the Firm continues to provide guidance to prospective business owners hoping to traverse the ever-changing landscape of recreational cannabis in areas including licensing, intellectual property, employment rights and municipal zoning and approval. Indeed, nearly 1,100 dispensary, manufacturing and cultivation licenses have been awarded to date.

About Ansell Grimm & Aaron, PC

Ansell Grimm & Aaron, PC was founded in 1929 and has a long history of delivering for clients who come to us to resolve legal matters that are often urgent, stressful, and of great importance. A general practice law firm, Ansell Grimm & Aaron is powered by experienced attorneys who understand that the best outcome is the one that serves the needs of each client.

Ansell’s dedicated Controlled Substances & Regulatory Law Practice Group has an in-depth understanding of the laws related to the production, sale, use, regulation and legalization of controlled substances, including:  hemp, cannabis, and psychedelics. Controlled substances law remains a multifaceted and complex field with, at times, conflicting regulations from different governing bodies.  Our attorneys are prepared to assist in all aspects of this emerging field and are committed to helping our clients understand their rights and the opportunities in this complex and evolving area of law.  For additional information, please contact Joshua S. Bauchner at (973) 247-9000 or jb@ansellgrimm.com.

 

The above is for informational purposes only and does not constitute legal advice. Transmission of the materials and information contained herein is not intended to create, and receipt thereof does not constitute the formation of, an attorney-client relationship. Attorney advertising.

CONTROLLED SUBSTANCES & REGULATORY LAW UPDATE – JANUARY 2022

New York Lawmakers Introduce Psychedelics Legalization Bill

New York state lawmakers introduced a bill to legalize natural psychedelics including psilocybin.  A.B. 114, originally intended to be introduced in the 2023-2024 legislative session, was proposed last week by Democratic Assembly members Linda Rosenthal, Jo Anne Simon, and Karines Reyes, according to a report from Marijuana Moment.

If passed, the bill would amend New York state law to legalize the “possession, use, cultivation, production, creation, analysis, gifting, exchange, or sharing by or between natural persons of twenty-one years of age or older of a natural plant or fungus-based hallucinogen.”  Included in the “plant or fungus based hallucinogens,” covered by the bill are DMT, mescaline, psilocybin and psilocin.

In recognition of the rapidly evolving perception of plant and fungus-based hallucinogens, the proposed bill also seeks to remove these drugs from Schedule 1 of New York’s list of controlled substances, offers legal protections to individuals who lawfully use natural psychedelics, and prohibits state and local law enforcement agencies from cooperating with U.S. agencies which criminalize natural psychedelic drugs.

New Jersey’s Psilocybin Behavioral Health Access and Services Act Seeks Legalization and Home Growth of Psilocybin

New Jersey Assembly Bill 4911, introduced to the Senate and Assembly, would decriminalize psilocybin, authorize personal use, and expungements for certain offenses involving psilocybin production, possession and distribution.

Titled the “Psilocybin Behavioral Health Access and Services Act,” the legislation would legalize the possession and distribution of up to 4 grams of psilocybin for adults 21 and over, and allow adults to cultivate mushrooms capable of producing psilocybin for personal use.

The proposed law also would create the Department of Health Psilocybin Behavioral Health Access and Services Advisory Board to oversee the process, a legal and regulatory structure to establish psilocybin service centers for treating patients, and for the commercial production of psilocybin.

Ansell’s Psychedelics Practice

On the heels of its successful cannabis practice, which has included numerous granted licenses for its clients as well as successes in Court litigating cannabis matters, last year the Firm expanded into the realm of psychedelics.

The Firm has an established record in the cannabis space enabling us to serve our clients unlike any other area law firm. By example, we co-hosted the first-ever Cannabis Symposium in New Jersey which drew nearly a thousand people (two other Symposia followed). Joshua S. Bauchner, head of the practice group, is co-chair of the New Jersey State Bar Association Cannabis Law Committee, has spoken at the Cannabis World Congress and Business Expo at the Jacob Javits Center, and has presented CLE’s on cannabis at the NY and NJ State Bar Associations, and at the NORML Legal Conference in Aspen, among other fora across the country.  He also recently was honored by the New Jersey Law Journal as one of its “2022 Innovators of the Year” for his work in the controlled substances space.

The Firm also was honored by the New Jersey Cannabis Insider as one of three finalists for Excellence in Cannabis Law and has been covered by numerous media outlets and published widely on the topic.

Please contact Joshua Bauchner (jb@ansellgrimm.com) or Kelsey Barber (kbarber@ansellgrimm.com) or call (973) 247-9000 if you are interested in exploring opportunities in the legalized psychedelics arena.

 

 

 

CONTROLLED SUBSTANCES & REGULATORY LAW REVIEW – 2022

In 2022, the Firm’s Controlled Substances and Regulatory Law Practice Group continues its rapid evolution and expansion. Our attorneys have assisted clients in applications for licensure, litigation to ensure transparency and integrity in the licensing process at the State and municipal levels, educational initiatives throughout the country, and entry into the developing area concerning legalization of psilocybin.

Ansell Launches Psychedelics Practice

On the heels of its successful cannabis practice, which has included numerous granted licenses for its clients as well as successes in Court litigating cannabis matters, the Firm recent announced it is expanding into the realm of psychedelics.

The Firm has an established record in the cannabis space enabling us to serve our clients unlike any other area law firm. By example, we co-hosted the first-ever Cannabis Symposium in New Jersey which drew nearly a thousand people (two other Symposia followed). Joshua S. Bauchner, head of the practice group, is co-chair of the New Jersey State Bar Association Cannabis Law Committee, has spoken at the Cannabis World Congress and Business Expo at the Jacob Javits Center, and has presented CLE’s on cannabis at the NY and NJ State Bar Associations, and at the NORML Legal Conference in Aspen, among other fora across the country.  He also recently was honored by the New Jersey Law Journal as one of its “Innovators of the Year” for 2022.

The Firm also was honored by the New Jersey Cannabis Insider as one of three finalists for Excellence in Cannabis Law and has been covered by numerous media outlets and published on the topic.

Now, with the federal government and many states looking to legalize psychedelics, Ansell is expanding the practice to include this emerging area of law. Please contact us at (973) 247-9000 if you are interested in exploring opportunities.

Cannabis Litigation — Securing Our Clients’ Rights

The Firm has been involved in several important lawsuits involving the State of New Jersey’s medicinal and adult use cannabis programs.  Additionally,

On the medicinal cannabis side, the Firm filed a new appeal with the Appellate Division on behalf of GGB New Jersey LLC (“GGB”) (now known as “The Source”) with respect to the 2019 RFA.  By way of background, in November 2020, the Appellate Division vacated the Department of Health’s (the “Department”) initial scoring of GGB’s application (and those similarly situated) seeking to operate vertically integrated alternative treatment centers because:  “There is no escaping the fact that some of these scores simply ‘don’t compute’ and that, no matter how the Department and the other respondents may attempt to slice it, the results are still unsettling.”  In the Matter of the Application for Medicinal Marijuana Alt. Treatment Ctr. for Pangaea Health & Wellness, LLC (“In re Pangaea”), 465 N.J. Super. 343, 371 (App. Div. 2020).  Accordingly, the Court held that GGB and others “were not afforded the process due under the applicable legislation and the Administrative Procedure Act, and we remand so the Department may provide that process.”  Id. at 382.  The Court noted that it intervened “in the administrative proceedings that have taken place so far to ensure the public’s confidence in both the results achieved at the agency level so far and to ensure that future similar proceedings will be likewise subjected to a measure of scrutiny at the agency level that will guarantee the process does not produce determinations that are arbitrary, capricious or unreasonable.”  Id. at 382-83.

After the Court-ordered remand process, the Commission refused to modify or adjust a single score and attempted to justify the Department’s original scoring on various grounds, none of which had any merit.  In the new appeal, GGB argued, among other things, that the Commission ignored the Appellate Division’s concerns about the unacceptably large degree of relative error and shockingly claimed that judicial review was unnecessary because “the scoring was what [the Commission] said it was[.]”  To prevent further delay by the Commission, GGB requested that the Court again vacate the agency decisions under review and, this time, remand with instructions to appoint a special master or administrative law judge to issue a report and recommendation that the Commission must adopt, modify, or reject by a date certain.

In light of the important public interest, the Appellate Division has accelerated this appeal and oral argument is likely to occur in the first quarter of 2023.

Turning to the recreational cannabis side, the Firm filed several cases against various municipalities that issued resolutions of support for cannabis applications pending before the Commission.  By way of background, the resolution of support requirement comes from the New Jersey Cannabis Regulatory, Enforcement Assistance, and Marketplace Modernization Act (“CREAMMA”), which provides, among other things, that an applicant establish “proof of local support for the suitability of the location, which may be demonstrated by a resolution adopted by the municipality’s governing body indicating that the intended location is appropriately located or otherwise suitable for such activities related to the cultivation, manufacturing, or dispensing of medical cannabis, cannabis products, and related supplies as will be conducted at the proposed facility.” N.J.S.A. 24:6I-7.2d(4)(c).

Keyport

The Firm has two cases pending against the Borough of Keyport (“Borough”).  On November 9, 2021, the Borough adopted Ordinance #15-21 to allow for the operation of a limited number of cannabis businesses subject to certain conditions (“Ordinance”).  The Ordinance provided that the Borough would issue a maximum of two (2) Class 5 cannabis retailer licenses.  The Borough later determined that one of the two available Class 5 cannabis retailer licenses would be for the highway commercial district and the other would be for the general commercial district.

The first case, which was filed on behalf of KGNJ Operations LLC (“KGNJ”), concerns the resolution of support granted to Blaze Keyport LLC for the highway commercial district.  The Firm asserted that the Borough’s decision was unsustainable because (1) it failed to use the evaluation sheets that it led applicants to believe would be used to score their applications, (2) only one member of the five-member subcommittee actually completed an evaluation sheet and only with respect to KGNJ’s application (and that member gave KGNJ a perfect score), and (3) the notes from the executive session of the Borough Council show that arbitrary, subjective, and biased criteria were applied to the deliberative process.  On December 7, 2022, the Superior Court held a hearing and ordered that the matter proceed on an accelerated basis with a trial scheduled for January or February 2023.

Another case, which was filed on behalf of Green and Gold Dispensary LLC (“G&G”), concerns the resolution of support granted to Simply Pure Keyport LLC for the general commercial district.  The Firm again argued that the Borough’s decision was arbitrary, capricious, and unreasonable because the selected applicant’s proposed location was within 150 feet measured “door-to-door” of La Iglesia Episcopal Santa Maria (St. Mary’s Episcopal Church) — remarkably, the church is two doors down the road — which was in direct violation of a Borough Ordinance prohibiting a cannabis facility from being located within 150 feet of a church, synagogue, temple or other place used exclusively for religious worship.  This matter is currently pending before the Superior Court.

Neptune City

The Firm also initiated a matter on behalf of The Cannabis Shoppe, LLC against the Borough of Neptune City (“Borough”).  There, the Firm asserted that the Borough improperly granted resolutions of support to two applicants who sought to establish Class 5 cannabis retailers within 400 feet walking distance of each other because the relevant ordinance expressly states that no retailer “shall be permitted within 600 feet” of any other retailer.  To make matters worse, both of the selected applicants’ proposed locations are immediately adjacent to residential neighborhoods and one of them was next to a bar.  This matter is currently pending before the Superior Court.

 

2022 Licenses Secured

We are happy to support and celebrate our clients’ securing cannabis licenses in 2022, and we are delighted to continue to assist with their developing businesses for a successful 2023 and beyond.

  1. Mule Extracts, LLC: Annual Manufacturer License

  2. Arbory Wellness, LLC: Annual Retailer License

  3. Canopy Crossroad: Microbusiness Retailer License

  4. The Violet Room: Annual Retailer License

  5. DMW Holdings LLC: Annual Manufacturer License

 

New York Medical Psilocybin Proposed Legislation – Regulatory Update

 New York legislators recently presented a modified bill to decriminalize psilocybin — the psychoactive ingredient in psychedelic mushrooms (Psilocybe cubensis) — for medicinal use in adults twenty-one and older. The proposed bill outlines a regulatory framework where psilocybin may be grown legally, provides a structure for treatment facilities to be established, implements standards for research facilities, and imposes guidelines for the certification of providers.

The proposed rules establish and oversee the implementation of several license types:

  • Designated caregiver facilities must register with the Department of Health to acquire, possess, transport, and administer medical psilocybin to certified patients, the rules outline the acceptable facilities and registration requirements.
  • Registered psilocybin organizations (“RPOs”), which are entities (for-profit and not-for-profit) that will grow, manufacture, possess, deliver, transport, and distribute psilocybin to designated caregiver facilities for medical use.
  • Psilocybin research license, which would permit a licensee to produce, process, purchase and/or possess psilocybin for limited research purposes.

The proposed bill also provides protections from criminal and civil penalties or disciplinary action for certified patients, caregiver facilities and their employees, practitioners, RPOs and researchers for the certified use or any other action in connection with the proposed rules. As a combined effort by the Commissioner of Health and the Comptroller, the rules would amend finance laws creating a “Psilocybin Therapy Grant Program Fund” to provide assistance to low-income individuals, veterans, and first responders with covered conditions under the law to receive financial assistance for psilocybin therapy.

The revised bill uses a similar methodology as the Marihuana Regulation and Taxation Act (“MRTA”), allowing for a social equity component for minority and women-owned businesses and distinguishing between various license types which may serve as a guide to how the use of medical psilocybin will be regulated in the future. Currently, psilocybin is categorized as a Schedule I controlled substance, which means it is illegal under federal law and considered to have a high potential for abuse with no accepted medical benefits. Proponents of the regulations believe that it could provide for much needed access to patients in a safe environment that is supervised by medical professionals.

The Firm’s Controlled Substance and Regulatory Law Practice Group assists clients interested in this emerging field which is likely to follow the lead of cannabis legalization — an area in which the firm has significant experience.

 

Federal Injunction Causes Uncertainty for Adult Use Cannabis in New York

New York recently issued its first 36 recreational cannabis licenses of 175 the state plans to issue, taking a monumental step in establishing a lucrative cannabis market. The first licenses approved by the state’s Cannabis Control Board were dedicated to “social equity” applicants, people who have been convicted of a cannabis-related crime – or have a family member who was – and have also run a profitable business for at least two years.

However, uncertainty has begun to plague New York’s potential expansion. On November 3, Judge Gary L. Sharpe of the U.S. District Court for the Northern District of New York issued a preliminary injunction, restricting the Office of Cannabis Management from issuing any cannabis licenses in five of the 14 regions in which the agency is licensing Conditional Adult Use Retail Dispensaries (CAURD). The injunction applies to CAURD applicants in the Finger Lakes, Central New York, Western New York, Mid-Hudson and Brooklyn.

Variscite NY One, Inc. (Variscite) the challenger, applied for a retail license, but its 51% principal owner failed to meet two New York-nexus requirements.  Under the New York program, a for-profit organization must, among other things, be “[a]t least 51% or more … owned, in the aggregate” by “at least one individual that satisfies” (1) a New York “significant presence” requirement and (2) a “justice involved” requirement, which asks whether the applicant (or a family member or dependent) “was convicted of a marihuana-related offense in New York State.” 9 N.Y.C.R.R. § 116.4(b)(1)(i).

Judge Sharpe agreed with Variscite and granted the preliminary injunction, finding that the program “will have a discriminatory effect on out-of-state residents seeking a CAURD [cannabis retail] license.” In a later footnote, Judge Sharpe stated that he thinks the law is patently unconstitutional.

The result of the federal injunction has left cannabis growers with over half a billion dollars’ worth of cannabis ready to sell, without any buyers. When asked about the farm’s concerns, the Office of Cannabis Management said the timeline remains the same and that they are “incredibly proud of our local family farmers, and excited for New Yorkers to begin sampling this tested, sun-grown cannabis.”

It remains to be seen whether cannabis retailers will be up and running by the end of the year, as promised by the Office of Cannabis Management.

 

 

About Ansell Grimm & Aaron, PC
Ansell Grimm & Aaron, PC was founded in 1929 and has a long history of delivering for clients who come to us to resolve legal matters that are often urgent, stressful, and of great importance. A general practice law firm, Ansell Grimm & Aaron is powered by experienced attorneys who understand that the best outcome is the one that serves the needs of each client.

About the Controlled Substances and Regulatory Law Practice Group

Among the leading controlled substances firms on the East Coast, we work with cannabis entrepreneurs, industrial hemp producers, psilocybin entrepreneurs, ancillary businesses and governing bodies seeking regulatory counsel.

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