24:6I-7.2 Submission of applications to commission.
24:6I-7.2 Submission of applications to commission.
12. a. Each application for a medical cannabis cultivator permit, medical cannabis manufacturer permit, and medical cannabis dispensary permit, and each application for annual renewal of such permit, including permit and renewal applications for microbusinesses that meet the requirements of subsection e. of section 11 of P.L.2019, c.153 (C.24:6I-7.1), shall be submitted to the commission. A full, separate application shall be required for each initial permit requested by the applicant and for each location at which an applicant seeks to operate, regardless of whether the applicant was previously issued a medical cannabis cultivator, medical cannabis manufacturer, medical cannabis dispensary, or clinical registrant permit, and regardless of whether the applicant currently holds a medical cannabis cultivator, medical cannabis manufacturer, or medical cannabis dispensary permit. Renewal applications shall be submitted to the commission on a form and in a manner as shall be specified by the commission no later than 90 days before the date the current permit will expire.
b. An initial permit application shall be evaluated according to criteria to be developed by the commission. The commission shall determine the point values to be assigned to each criterion, which shall include bonus points for applicants who are residents of New Jersey.
c. The criteria to be developed by the commission pursuant to subsection b. of this section shall include, in addition to the criteria set forth in subsections d. and e. of this section and any other criteria developed by the commission, an analysis of the applicant's operating plan, excluding safety and security criteria, which shall include the following:
(1) In the case of an applicant for a medical cannabis cultivator permit, the operating plan summary shall include a written description concerning the applicant's qualifications for, experience in, and knowledge of each of the following topics:
(a) State-authorized cultivation of medical cannabis;
(b) conventional horticulture or agriculture, familiarity with good agricultural practices, and any relevant certifications or degrees;
(c) quality control and quality assurance;
(d) recall plans;
(e) packaging and labeling;
(f) inventory control and tracking software or systems for the production of medical cannabis;
(g) analytical chemistry and testing of medical cannabis;
(h) water management practices;
(i) odor mitigation practices;
(j) onsite and offsite recordkeeping;
(k) strain variety and plant genetics;
(l) pest control and disease management practices, including plans for the use of pesticides, nutrients, and additives;
(m) waste disposal plans; and
(n) compliance with applicable laws and regulations.
(2) In the case of an applicant for a medical cannabis manufacturer permit, the operating plan summary shall include a written description concerning the applicant's qualifications for, experience in, and knowledge of each of the following topics:
(a) State-authorized manufacture and creation of cannabis products using appropriate extraction methods, including intended use and sourcing of extraction equipment and associated solvents or intended methods and equipment for non-solvent extraction;
(b) pharmaceutical manufacturing, good manufacturing practices, and good laboratory practices;
(c) quality control and quality assurance;
(d) recall plans;
(e) packaging and labeling;
(f) inventory control and tracking software or systems for the production of medical cannabis;
(g) analytical chemistry and testing of medical cannabis and medical cannabis products and formulations;
(h) water management practices;
(i) odor mitigation practices;
(j) onsite and offsite recordkeeping;
(k) a list of product formulations or products proposed to be manufactured with estimated cannabinoid profiles, if known, including varieties with high cannabidiol content;
(l) intended use and sourcing of all non-cannabis ingredients used in the manufacture and creation of cannabis products, including methods to verify or ensure the safety and integrity of those ingredients and their potential to be or contain allergens;
(m) waste disposal plans; and
(n) compliance with applicable laws and regulations.
(3) In the case of an applicant for a medical cannabis dispensary permit, the operating plan summary shall include a written description concerning the applicant's qualifications for, experience in, and knowledge of each of the following topics:
(a) State-authorized dispensation of medical cannabis to qualifying patients;
(b) healthcare, medicine, and treatment of patients with qualifying medical conditions;
(c) medical cannabis product evaluation procedures;
(d) recall plans;
(e) packaging and labeling;
(f) inventory control and point-of-sale software or systems for the sale of medical cannabis;
(g) patient counseling procedures;
(h) the routes of administration, strains, varieties, and cannabinoid profiles of medical cannabis and medical cannabis products;
(i) odor mitigation practices;
(j) onsite and offsite recordkeeping;
(k) compliance with State and federal patient privacy rules;
(l) waste disposal plans; and
(m) compliance with applicable laws and regulations.
d. The criteria to be developed by the commission pursuant to subsection b. of this section shall include, in addition to the criteria set forth in subsections c. and e. of this section and any other criteria developed by the commission, an analysis of the following factors, if applicable:
(1) The applicant's environmental impact plan.
(2) A summary of the applicant's safety and security plans and procedures, which shall include descriptions of the following:
(a) plans for the use of security personnel, including contractors;
(b) the experience or qualifications of security personnel and proposed contractors;
(c) security and surveillance features, including descriptions of any alarm systems, video surveillance systems, and access and visitor management systems, along with drawings identifying the proposed locations for surveillance cameras and other security features;
(d) plans for the storage of medical cannabis and medical cannabis products, including any safes, vaults, and climate control systems that will be utilized for this purpose;
(e) a diversion prevention plan;
(f) an emergency management plan;
(g) procedures for screening, monitoring, and performing criminal history record background checks of employees;
(h) cybersecurity procedures, including, in the case of an applicant for a medical cannabis dispensary permit, procedures for collecting, processing, and storing patient data, and the applicant's familiarity with State and federal privacy laws;
(i) workplace safety plans and the applicant's familiarity with federal Occupational Safety and Health Administration regulations;
(j) the applicant's history of workers' compensation claims and safety assessments;
(k) procedures for reporting adverse events; and
(l) a sanitation practices plan.
(3) A summary of the applicant's business experience, including the following, if applicable:
(a) the applicant's experience operating businesses in highly-regulated industries;
(b) the applicant's experience in operating alternative treatment centers and related medical cannabis production and dispensation entities under the laws of New Jersey or any other state or jurisdiction within the United States; and
(c) the applicant's plan to comply with and mitigate the effects of 26 U.S.C. s.280E on cannabis businesses, and for evidence that the applicant is not in arrears with respect to any tax obligation to the State.
In evaluating the experience described under subparagraphs (a), (b), and (c) of this paragraph, the commission shall afford the greatest weight to the experience of the applicant itself, controlling owners, and entities with common ownership or control with the applicant; followed by the experience of those with a 15 percent or greater ownership interest in the applicant's organization; followed by significantly involved persons in the applicant's organization; followed by other officers, directors, and current and prospective employees of the applicant who have a bona fide relationship with the applicant's organization as of the date of the application.
(4) A description of the proposed location for the applicant's site, including the following, if applicable:
(a) the proposed location, the surrounding area, and the suitability or advantages of the proposed location, along with a floor plan and optional renderings or architectural or engineering plans;
(b) the submission of zoning approvals for the proposed location, which shall consist of a letter or affidavit from appropriate municipal officials that the location will conform to municipal zoning requirements allowing 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; and
(c) the submission of 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.
Notwithstanding any other provision of this subsection, an application shall be disqualified from consideration unless it includes documentation demonstrating that the applicant will have final control of the premises upon approval of the application, including, but not limited to, a lease agreement, contract for sale, title, deed, or similar documentation. In addition, if the applicant will lease the premises, the application will be disqualified from consideration unless it includes certification from the landlord that the landlord is aware that the tenant's use of the premises will involve activities related to the cultivation, manufacturing, or dispensing of medical cannabis and medical cannabis products. An application shall not be disqualified from consideration if the application does not include the materials described in subparagraph (b) or (c) of this paragraph.
(5) A community impact, social responsibility, and research statement, which shall include, but shall not be limited to, the following:
(a) a community impact plan summarizing how the applicant intends to have a positive impact on the community in which the proposed entity is to be located, which shall include an economic impact plan, a description of outreach activities, and any financial assistance or discount plans the applicant will provide to qualifying patients and designated caregivers;
(b) a written description of the applicant's record of social responsibility, philanthropy, and ties to the proposed host community;
(c) a written description of any research the applicant has conducted on the medical efficacy or adverse effects of cannabis use and the applicant's participation in or support of cannabis-related research and educational activities; and
(d) a written plan describing any research and development regarding the medical efficacy or adverse effects of cannabis, and any cannabis-related educational and outreach activities, which the applicant intends to conduct if issued a permit by the commission.
In evaluating the information submitted pursuant to subparagraphs (b) and (c) of this paragraph, the commission shall afford the greatest weight to responses pertaining to the applicant itself, controlling owners, and entities with common ownership or control with the applicant; followed by responses pertaining to those with a 15 percent or greater ownership interest in the applicant's organization; followed by significantly involved persons in the applicant's organization; followed by other officers, directors, and current and prospective employees of the applicant who have a bona fide relationship with the applicant's organization as of the date of the application.
(6) A workforce development and job creation plan, which may include information on the applicant's history of job creation and planned job creation at the proposed facility; education, training, and resources to be made available for employees; any relevant certifications; and a diversity plan.
(7) A business and financial plan, which may include, but shall not be limited to, the following:
(a) an executive summary of the applicant's business plan;
(b) a demonstration of the applicant's financial ability to implement its business plan, which may include, but shall not be limited to, bank statements, business and individual financial statements, net worth statements, and debt and equity financing statements; and
(c) a description of the applicant's plan to comply with guidance pertaining to cannabis issued by the Financial Crimes Enforcement Network under 31 U.S.C. s.5311 et seq., the federal "Bank Secrecy Act", which may be demonstrated by submitting letters regarding the applicant's banking history from banks or credit unions that certify they are aware of the business activities of the applicant, or entities with common ownership or control with the applicant, in any state where the applicant has operated a business related to medical cannabis. For the purposes of this subparagraph, the commission shall consider only bank references involving accounts in the name of the applicant or of an entity with common ownership or control with the applicant. An applicant who does not submit the information described in this subparagraph shall not be disqualified from consideration.
(8) Whether any of the applicant's majority or controlling owners were previously approved by the commission to serve as an officer, director, principal, or key employee of an alternative treatment center, or personal use cannabis establishment, distributor, or delivery service, provided any such individual served in that capacity at the alternative treatment center for six or more months.
(9) Whether the applicant can demonstrate that its governance structure includes the involvement of a school of medicine or osteopathic medicine licensed and accredited in the United States, or a general acute care hospital, ambulatory care facility, adult day care services program, or pharmacy licensed in New Jersey, provided that:
(a) the school, hospital, facility, or pharmacy has conducted or participated in research approved by an institutional review board related to cannabis involving the use of human subjects, except in the case of an accredited school of medicine or osteopathic medicine that is located and licensed in New Jersey;
(b) the school, hospital, facility, or pharmacy holds a profit share or ownership interest in the applicant's organization of 10 percent or more, except in the case of an accredited school of medicine or osteopathic medicine that is located and licensed in New Jersey; and
(c) the school, hospital, facility, or pharmacy participates in major decision-making activities within the applicant's organization, which may be demonstrated by representation on the board of directors of the applicant's organization.
(10) The proposed composition of the applicant's medical advisory board established pursuant to section 15 of P.L.2019, c.153 (C.24:6I-7.5), if any.
(11) Whether the applicant intends to or has entered into a partnership with a prisoner re-entry program for the purpose of identifying and promoting employment opportunities at the applicant's organization for former inmates and current inmates leaving the corrections system. If so, the applicant shall provide details concerning the name of the re-entry program, the employment opportunities at the applicant's organization that will be made available to the re-entry population, and any other initiatives the applicant's organization will undertake to provide support and assistance to the re-entry population.
(12) Any other information the commission deems relevant in determining whether to grant a permit to the applicant.
e. In addition to the information to be submitted pursuant to subsections c. and d. of this section, the commission shall require all permit applicants, other than applicants for a conditional permit, or for an entity that is a microbusiness pursuant to subsection e. of section 11 of P.L.2019, c.153 (C.24:6I-7.1), to submit an attestation signed by a bona fide labor organization stating that the applicant has entered into a labor peace agreement with such bona fide labor organization. Except in the case of an entity holding an unconverted conditional permit, the maintenance of a labor peace agreement with a bona fide labor organization shall be an ongoing material condition of maintaining a medical cannabis cultivator, medical cannabis manufacturer, or medical cannabis dispensary permit. The submission of an attestation and maintenance of a labor peace agreement with a bona fide labor organization by an applicant issued a conditional permit pursuant to subsection d. of section 11 of P.L.2019, c.153 (C.24:6I-7.1.) shall be a requirement for conversion of a conditional permit into a full permit. The failure to enter into a collective bargaining agreement within 200 days after the date that a medical cannabis cultivator, medical cannabis manufacturer, or medical cannabis dispensary first opens shall result in the suspension or revocation of such permit or conditional permit.
In reviewing initial permit applications, the commission shall give priority to the following, regardless of whether there is any competition among applicants for a particular type of permit:
(1) Applicants that are party to a collective bargaining agreement with a bona fide labor organization that currently represents, or is actively seeking to represent, cannabis workers in New Jersey.
(2) Applicants that are party to a collective bargaining agreement with a bona fide labor organization that currently represents cannabis workers in another state.
(3) Applicants that include a significantly involved person or persons lawfully residing in New Jersey for at least two years as of the date of the application.
(4) Applicants that submit a signed project labor agreement with a bona fide building trades labor organization, which is a form of pre-hire collective bargaining agreement covering terms and conditions of a specific project, including labor issues and worker grievances associated with that project, for the construction or retrofit of the facilities associated with the permitted entity.
(5) Applicants that submit a signed project labor agreement with a bona fide labor organization for any other applicable project associated with the permitted entity.
As used in this subsection, "bona fide labor organization" means a labor organization of any kind or employee representation committee, group, or association, in which employees participate and which exists and is constituted for the purpose, in whole or in part, of collective bargaining or otherwise dealing with medical or personal use cannabis employers concerning grievances, labor disputes, terms or conditions of employment, including wages and rates of pay, or other mutual aid or protection in connection with employment, and may be characterized by: it being a party to one or more executed collective bargaining agreements with medical or personal use cannabis employers, in this State or another state; it having a written constitution or bylaws in the three immediately preceding years; it filing the annual financial report required of labor organizations pursuant to subsection (b) of 29 U.S.C. s.431, or it having at least one audited financial report in the three immediately preceding years; it being affiliated with any regional or national association of unions, including but not limited to state and federal labor councils; or it being a member of a national labor organization that has at least 500 general members in a majority of the 50 states of the United States. A bona fide labor organization includes a bona fide building trades labor organization.
f. In reviewing an initial permit application, unless the information is otherwise solicited by the commission in a specific application question, the commission's evaluation of the application shall be limited to the experience and qualifications of the applicant's organization, including controlling owners, any entities with common ownership or control with the applicant, those with a 15 percent or greater interest in the applicant's organization, significantly involved persons in the applicant's organization, the other officers, directors, and current or prospective employees of the applicant's organization who have a bona fide relationship with the applicant's organization as of the date of the application, and consultants and independent contractors who have a bona fide relationship with the applicant as of the date of the application. Responses pertaining to applicants who are exempt from the criminal history record background check requirements of section 7 of P.L.2009, c.307 (C.24:6I-7) shall not be considered. Each applicant shall certify as to the status of the individuals and entities included in the application.
g. The commission shall conduct a disparity study to determine whether race-based measures should be considered when issuing permits pursuant to this section, and shall incorporate the policies, practices, protocols, standards, and criteria developed by the Office of Minority, Disabled Veterans, and Women Cannabis Business Development pursuant to section 32 of P.L.2019, c.153 (C.24:6I-25) to promote participation in the medical cannabis industry by persons from socially and economically disadvantaged communities, including promoting applications for, and the issuance of, medical cannabis cultivator, medical cannabis manufacturer, and medical cannabis dispensary permits to certified minority, women's, and disabled veterans' businesses. To this end, the commission shall seek to issue at least 30 percent of the total number of new medical cannabis cultivator permits, medical cannabis manufacturer permits, and medical cannabis dispensary permits issued on or after the effective date of P.L.2019, c.153 (C.24:6I-5.1 et al.) as follows:
(1) at least 15 percent of the total number of new medical cannabis cultivator permits, medical cannabis manufacturer permits, and medical cannabis dispensary permits are issued to a qualified applicant that has been certified as a minority business pursuant to P.L.1986, c.195 (C.52:27H-21.18 et seq.); and
(2) at least 15 percent of the total number of new medical cannabis cultivator permits, medical cannabis manufacturer permits, and medical cannabis dispensary permits are issued to a qualified applicant that has been certified as a women's business pursuant to P.L.1986, c.195 (C.52:27H-21.18 et seq.) or as a disabled-veterans' business, as defined in section 2 of P.L.2015, c.116 (C.52:32-31.2).
In selecting among applicants who meet these criteria, the commission shall grant a higher preference to applicants with up to two of the certifications described in this subsection.
h. The commission shall give special consideration to any applicant that has entered into an agreement with an institution of higher education to create an integrated curriculum involving the cultivation, manufacturing, dispensing or delivery of medical cannabis, provided that the curriculum is approved by both the commission and the Office of the Secretary of Higher Education and the applicant agrees to maintain the integrated curriculum in perpetuity. An integrated curriculum permit shall be subject to revocation if the IC permit holder fails to maintain or continue the integrated curriculum. In the event that, because of circumstances outside an IC permit holder's control, the IC permit holder will no longer be able to continue an integrated curriculum, the IC permit holder shall notify the commission and shall make reasonable efforts to establish a new integrated curriculum with an institution of higher education, subject to approval by the commission and the Office of the Secretary of Higher Education. If the IC permit holder is unable to establish a new integrated curriculum within six months after the date the current integrated curriculum arrangement ends, the commission shall revoke the entity's IC permit, unless the commission finds there are extraordinary circumstances that justify allowing the permit holder to retain the permit without an integrated curriculum and the commission finds that allowing the permit holder to retain the permit would be consistent with the purposes of P.L.2009, c.307 (C.24:6I-1 et al.), in which case the IC permit shall convert to a regular permit of the same type. The commission may revise the application and permit fees or other conditions for an IC permit as may be necessary to encourage applications for IC permits.
i. Application materials submitted to the commission pursuant to this section shall not be considered a public record pursuant to P.L.1963, c.73 (C.47:1A-1 et seq.), P.L.2001, c.404 (C.47:1A-5 et al.), or the common law concerning access to government records.
j. If the commission notifies an applicant that it has performed sufficiently well on multiple applications to be awarded more than one permit, the applicant shall notify the commission, within seven business days after receiving such notice, as to which permit type it will accept. For any permit award declined by an applicant pursuant to this subsection, the commission shall, upon receiving notice from the applicant of the declination, award the permit to the applicant for that permit type who, in the determination of the commission, best satisfies the commission's criteria while meeting the commission's determination of Statewide need. If an applicant fails to notify the commission as to which permit it will accept, the commission shall have the discretion to determine which permit it will award to the applicant, based on the commission's determination of Statewide need and other applications submitted for facilities to be located in the affected regions.
k. (1) Subject to the provisions of paragraph (2) of this subsection, the provisions of this section shall not apply to any permit applications submitted pursuant to a request for applications published in the New Jersey Register prior to the effective date of P.L.2019, c.153 (C.24:6I-5.1 et al.).
(2) The provisions of subsection l. of this section shall not apply to any permit applications submitted pursuant to a request for applications published in the New Jersey Register prior to the effective date of P.L.2021, c.252.
l. In addition to the information to be submitted pursuant to subsections c., d., and e. of this section, the commission shall require all permit applicants to submit a copy of any services agreement entered into by the applicant with third party entity, which agreement shall be subject to review as provided in subsection f. of section 11 of P.L.2019, c.153 (C.24:6I-7.1).
L.2019, c.153, s.12; amended 2021, c.16, s.16; 2021. c.252, s.3.
Structure New Jersey Revised Statutes
Section 24:1-1.1 - Honey, raw, unprocessed.
Section 24:1-2 - Certain books as evidence
Section 24:1-3 - Responsibility for acts of officers and agents
Section 24:1-4 - Foods, drugs, etc., complying with Federal regulations
Section 24:2-1 - Enforcement by state departments; rules and regulations
Section 24:2-2 - Enforcement by local board
Section 24:2-3 - Appointment of analysts, chemists, specialists, chief inspectors, etc.
Section 24:2-5 - Powers, duties of registered environmental health specialist.
Section 24:2-6 - Interference with officials; penalties
Section 24:2-9 - Fees for issuance of "Certificate of Free Sale."
Section 24:3-1 - Right of entry; opening packages; inspection
Section 24:3-2 - Procuring sample of food or drug
Section 24:3-3 - Taking sample without consent of owner
Section 24:3-4 - Preservation of sample
Section 24:3-5 - Proof of analysis as evidence
Section 24:3-6 - Proof of analysis on purchase by other than representative of department
Section 24:3-9 - Composite sample of milk seized in transit
Section 24:4-1 - Confiscation; summary proceeding
Section 24:4-5 - Issuance of warrant
Section 24:4-8 - Claims under oath
Section 24:4-9 - Sale or destruction of condemned article
Section 24:4-10 - Return of goods; bond
Section 24:4-11 - Summary destruction of perishable food
Section 24:4-12 - Adulterated or misbranded foods, drugs, etc.; marking; detaining
Section 24:4A-2 - Definitions.
Section 24:4A-3 - Nonliability for food donated.
Section 24:4A-3.1 - Immunity from liability.
Section 24:4A-4 - Food banks; licenses; fee; regulation
Section 24:4A-4.1 - Online portal to facilitate surplus food donations.
Section 24:4A-5 - Rules and regulations
Section 24:4A-6 - "Healthy Small Food Retailer Act"
Section 24:4A-7 - Findings and declarations relative to small food retailers
Section 24:4A-8 - Definitions relative to small food retailers
Section 24:4A-9, - Implementation of "Healthy Corner Store Program"
Section 24:4A-10 - "Healthy Small Food Retailer Fund" established
Section 24:4A-11 - Grantee report
Section 24:4A-12 - "Jersey Fresh" website expansion
Section 24:4A-13 - Rules, regulations
Section 24:5-1 - Sale, distribution or manufacture of adulterated or misbranded articles
Section 24:5-3 - Content of guaranty; liability of resident seller
Section 24:5-4 - Guaranty by nonresident
Section 24:5-5 - Extent of protection of dealer
Section 24:5-6 - Article for foreign market
Section 24:5-7 - Sale of patent medicines not authorized
Section 24:5-8 - General food adulterations
Section 24:5-9 - Confectionery adulterations
Section 24:5-10 - General drug or device adulterations
Section 24:5-11 - Exceptions to drug adulterations
Section 24:5-11.1 - General cosmetic adulterations
Section 24:5-13 - Use of wood or methyl alcohol prohibited; penalty
Section 24:5-14 - Meat and meat products
Section 24:5-16 - "Misbranded" defined
Section 24:5-17 - Food misbrandings
Section 24:5-18 - Drug or device misbrandings.
Section 24:5-18.1 - Cosmetic misbrandings
Section 24:5-18.2 - Exemptions from labeling and packaging requirements
Section 24:5-19 - Drugs dispensed by physicians, etc., or on written prescription
Section 24:5-22 - Defacement or removal of label
Section 24:5-23 - Permit to process, manufacture product with hemp, transportation.
Section 24:5A-3 - Hazardous substance; limitation
Section 24:5A-4 - Application of Federal Hazardous Substances Labeling Act
Section 24:5A-5 - Commissioner; powers
Section 24:5A-6 - Prohibited acts
Section 24:5A-8 - Enforcement of act; penalties
Section 24:5A-9 - Action to restrain violations
Section 24:6-1 - Establishment of standards
Section 24:6-2 - Publication: time of taking effect
Section 24:6-3 - Sale or manufacture of nonstandard articles prohibited
Section 24:6B-1 - Registration statement, issuance of registration.
Section 24:6B-2 - Registration statement, signature, verification; form and contents.
Section 24:6B-3 - Time for filing
Section 24:6B-5 - Change of address; notice; fee
Section 24:6B-6 - Cleanliness of premises
Section 24:6B-7 - Cleanliness of equipment and machinery
Section 24:6B-8 - Washroom and toilet facilities
Section 24:6B-9 - Adulteration or misbranding of drug; examination of records
Section 24:6B-10 - Order to correct violation
Section 24:6B-12 - Definitions.
Section 24:6B-13 - Appropriation
Section 24:6B-14 - Definitions relative to pharmaceutical wholesale distributors.
Section 24:6B-15 - Licensure required for pharmaceutical wholesale distributors.
Section 24:6B-17 - Establishment, maintenance of list of authorized distributors.
Section 24:6B-18 - Determination of eligibility for licensure renewal.
Section 24:6B-19 - Additional requirements for designated representatives.
Section 24:6B-20 - Requirements for facilities used for wholesale prescription drug distribution.
Section 24:6B-21 - Provision of pedigree, certification prior to sale, return of prescription drug.
Section 24:6B-22 - Annual report to the Legislature on tracking system.
Section 24:6B-23 - Authentication of distribution of prescription drug.
Section 24:6B-24 - Examination of shipping container.
Section 24:6B-25 - Criteria for return of prescription drug to wholesale distributor.
Section 24:6B-26 - Requirements for wholesale distributor.
Section 24:6B-27 - Maintenance of document, record relative to pedigree, certification.
Section 24:6B-28 - Adherence to written policies, procedures by wholesale distributors.
Section 24:6B-29 - Violations, gradation of offenses.
Section 24:6B-30 - Noncompliance with orders, penalties.
Section 24:6B-31 - Real, personal property, certain, subject to forfeiture.
Section 24:6B-32 - Wholesale Drug Distribution Advisory Council.
Section 24:6B-33 - Rules, regulations.
Section 24:6E-2 - Advertisement of prescription drugs; rules and regulations
Section 24:6E-3 - Restraint on prescription drug price information to public
Section 24:6E-4 - Definitions.
Section 24:6E-6 - List of interchangeable drug products.
Section 24:6E-9 - Dispensation of nonbrand name drug product; label.
Section 24:6E-13 - Severability
Section 24:6F-5 - Records on use; periodic studies
Section 24:6G-1 - Control or possession without written permit; prohibition; exceptions
Section 24:6G-2 - Sale of nitrous oxide for nonmedical use
Section 24:6G-3 - Record of sale; duration of retention; contents; inspection
Section 24:6G-4 - Permits; purposes authorized
Section 24:6G-5 - Administration and enforcement; rules
Section 24:6G-6 - Violations; penalties; recovery and enforcement
Section 24:6H-1 - Distribution of ephedrine alkaloids to minor, disorderly person; exceptions.
Section 24:6H-2 - Label required on ephedrine alkaloid products.
Section 24:6H-3 - Rules, regulations.
Section 24:6I-1 - Short title.
Section 24:6I-2 - Findings, declarations relative to the medical use of cannabis.
Section 24:6I-3 - Definitions relative to the medical use of cannabis.
Section 24:6I-4 - Registry of qualifying patients, designated, institutional caregivers.
Section 24:6I-5.1 - Authorization process for dispensation.
Section 24:6I-5.2 - Health care practitioner, regulations affecting.
Section 24:6I-5.3 - Qualifying patient from another state, jurisdiction.
Section 24:6I-6 - Applicability of N.J.S.2C:35-18.
Section 24:6I-6.1 - Adverse employment action unlawful.
Section 24:6I-7 - Applications for permits.
Section 24:6I-7.1 - Acceptance, processing of applications.
Section 24:6I-7.2 - Submission of applications to commission.
Section 24:6I-7.3 - Clinical registrant permits.
Section 24:6I-7.5 - Medical advisory board.
Section 24:6I-7.6 - Ineligibility for certain economic incentives.
Section 24:6I-8 - Inapplicability.
Section 24:6I-9 - Falsification of registration card, degree of crime.
Section 24:6I-11 - Grants, contributions, use of fees.
Section 24:6I-12 - Reports to Governor, Legislature.
Section 24:6I-13 - Exchange of data, information.
Section 24:6I-14 - Construction of act.
Section 24:6I-15 - Additional immunity.
Section 24:6I-16 - Rules, regulations.
Section 24:6I-17 - Testing of cannabis.
Section 24:6I-18 - Licensing of testing laboratories.
Section 24:6I-19 - Standardized requirements, procedures for testing.
Section 24:6I-20 - Medical cannabis handler certification.
Section 24:6I-21 - Municipalities may authorize consumption areas.
Section 24:6I-22 - System for tracking, cultivating, manufacturing, transfer, dispensing, delivery.
Section 24:6I-23 - Requirements waived by commission.
Section 24:6I-24 - Cannabis Regulatory Commission.
Section 24:6I-25 - Office of Minority, Disabled Veterans, and Women Cannabis Business Development.
Section 24:6I-26 - Criteria for eligibility as employee.
Section 24:6I-27 - Applicability of C.52:13D-12 et seq.; Code of Ethics.
Section 24:6I-28 - Restrictions for commission members, employees.
Section 24:6I-29 - Certain persons prohibited from association with medical cannabis.
Section 24:6I-30 - Severability.
Section 24:6I-31 - Short title.
Section 24:6I-32 - Findings, declarations relative to the regulation and use of cannabis.
Section 24:6I-33 - Definitions relative to the regulation and use of cannabis.
Section 24:6I-34 - Commission activities associated with the personal use of cannabis.
Section 24:6I-35 - Regulation of cannabis.
Section 24:6I-36 - Application for license of conditional license.
Section 24:6I-37 - Class I Cannabis Cultivator license.
Section 24:6I-38 - Grow canopies for licensed cannabis cultivators.
Section 24:6I-39 - Class 2 cannabis manufacturer license.
Section 24:6I-40 - Class 3 cannabis wholesaler license.
Section 24:6I-41 - Class 4 cannabis distributor license.
Section 24:6I-42 - Class 5 cannabis retailer license.
Section 24:6I-43 - Class 6 cannabis delivery license.
Section 24:6I-45 - Municipal regulations or ordinances.
Section 24:6I-46 - Marketplace regulation.
Section 24:6I-47 - Medical cannabis provisions.
Section 24:6I-48 - Medical cannabis - additional regulatory requirements.
Section 24:6I-50 - Cannabis regulatory, enforcement assistance, and marketplace modernization fund.
Section 24:6I-51 - Licensee and consumer protections.
Section 24:6I-52 - Employers, driving, minors and control of property.
Section 24:6I-53 - Contract enforceability.
Section 24:6I-54 - Federal and interstate relations.
Section 24:6I-55 - Limitations.
Section 24:6I-56 - Severability.
Section 24:6J-1 - Short title.
Section 24:6J-2 - Findings, declarations relative to overdose prevention.
Section 24:6J-3 - Definitions relative to overdose prevention.
Section 24:6J-4 - Immunity from liability for certain prescribers, practitioners, dispensers.
Section 24:6J-5 - Overdose prevention information.
Section 24:6J-5.1 - Provision of certain information to victims of opioid overdoses; definitions.
Section 24:6J-6 - Awarding of grants.
Section 24:6J-7 - Opioid antidotes, recognized place of public access.
Section 24:6K-1 - Definitions relative to dispensing certain biological products.
Section 24:6K-2 - Link to current lists of all biological products.
Section 24:6K-3 - Conditions for substitution.
Section 24:6K-4 - Rules, regulations.
Section 24:6L-1 - Short title.
Section 24:6L-2 - Findings, declarations relative to epinephrine auto-injectors.
Section 24:6L-3 - Definitions relative to epinephrine auto-injectors.
Section 24:6L-4 - Authorization to administer.
Section 24:6L-5 - Written standards, application procedures.
Section 24:6L-6 - Immunity from civil liability, disciplinary action.
Section 24:6L-7 - Construction of act.
Section 24:6M-1 - Findings, declarations relative to drug donation.
Section 24:6M-2 - Definitions relative to drug donation.
Section 24:6M-3 - Establishment, maintenance of drug donation program.
Section 24:6M-4 - Conditions relative to program.
Section 24:6M-5 - Immunity from liability.
Section 24:6M-6 - Construction of act.
Section 24:6M-7 - Rules, regulations.
Section 24:6M-8 - Tax credit for donor.
Section 24:6M-9 - Tax credit for donor.
Section 24:8-1 - "Caustic acids" and "caustic alkalies" enumerated
Section 24:8-2 - Labeling containers of caustic acids and alkalies intended for household use
Section 24:9-22 - Application for license for refrigerated warehouse or locker plant
Section 24:9-23 - License fees; suspension or revocation of license
Section 24:9-24 - Reports to commissioner
Section 24:9-25 - Notice of insanitary condition of warehouse or locker plant
Section 24:9-26 - Duration of storage period; extension
Section 24:9-28 - Restorage after release from storage prohibited
Section 24:9-29 - Transfer between refrigerators
Section 24:9-30 - Requirements for storage
Section 24:9-31 - Lot numbers for identification
Section 24:9-32 - Marking and tagging of articles placed in storage
Section 24:9-33 - Alteration, mutilation or destruction of tags or marks prohibited
Section 24:9-34 - Penalties for violations
Section 24:9-35 - Enforcement of provisions
Section 24:9-36 - Plaintiff entitled to penalties
Section 24:10-57.1 - Definitions
Section 24:10-57.3 - Restrictions in permits
Section 24:10-57.4 - Temporary or emergency permits
Section 24:10-57.5 - Annual fee; amounts
Section 24:10-57.6 - Preliminary findings
Section 24:10-57.7 - Forms; establishment by state department
Section 24:10-57.8 - Revocation of permit; grounds; renewal; suspension pending hearing
Section 24:10-57.9 - Maintenance of records; inspection
Section 24:10-57.10 - Powers of local board of health
Section 24:10-57.11 - Inconsistent ordinances, rules or regulations
Section 24:10-57.12 - Notification of violations; prohibition of distribution and sale
Section 24:10-57.13 - Inspections; authorized inspectors
Section 24:10-57.14 - Place of inspection
Section 24:10-57.15 - Inability of local board to make inspections
Section 24:10-57.16 - Bacteriological and other tests; methods, techniques, personnel, etc.
Section 24:10-57.17 - Pasteurization required
Section 24:10-57.18 - Milk and fluid milk products; pasteurization
Section 24:10-57.19 - Enforcement; failure of local board to act; procedure by state department
Section 24:10-57.20 - Rules and regulations
Section 24:10-57.21 - Sanitary conditions; health and habits of personnel
Section 24:10-57.22 - Use of apparatus, containers, equipment, etc., for other purposes prohibited
Section 24:10-57.23 - Container regulations
Section 24:10-57.24b - Additional rules and regulations for milk products and their imitations
Section 24:10-57.26 - Failure of milk or milk products to meet minimum requirements
Section 24:10-57.27 - Milk and milk products of violators barred from state
Section 24:10-57.28 - Contamination of milk
Section 24:10-57.29 - Severability
Section 24:10-73.1a - Compliance with rules and regulations; extensions of time
Section 24:10-73.2 - "Frozen desserts" ; definition
Section 24:10-73.5 - Definitions.
Section 24:10-73.6 - Sale of adulterated frozen desserts prohibited
Section 24:10-73.7 - When frozen desserts deemed adulterated
Section 24:10-73.10 - License to sell, distribute frozen desserts.
Section 24:10-73.11 - Form of application; affidavit
Section 24:10-73.12 - Issuance of license; expiration
Section 24:10-73.13 - Revocation or suspension of license; renewal
Section 24:10-73.14 - Illegal sale and distribution of frozen dessert
Section 24:10-73.15 - Use of license moneys for enforcement
Section 24:10-73.16 - Inspection; fee
Section 24:10-73.17 - Partial invalidity
Section 24:10A-1 - Straws, tubes and other devices for drinking
Section 24:10A-2 - Rules and regulations
Section 24:10A-4 - Effective date
Section 24:11-1 - License; expiration
Section 24:11-2 - Revocation of license
Section 24:11-3 - Eggs unfit for food
Section 24:11-4 - Labeling "rots" and "spots"
Section 24:11-5 - Denatured eggs; labeling
Section 24:11-6 - Inspection of egg establishments
Section 24:11-7 - Distribution, sale, etc., of eggs removed from incubators
Section 24:11-8 - Penalty for violation
Section 24:11-9 - Enforcement of act
Section 24:11A-1 - Short title
Section 24:11A-2 - Declaration of purpose
Section 24:11A-3 - Definitions
Section 24:11A-4 - Flour; vitamin and mineral content; minimum standards
Section 24:11A-5 - Bread and rolls; vitamin and mineral content; minimum standards
Section 24:11A-6 - Enrichment; ingredients
Section 24:11A-9 - Enforcement of act; investigations and inspections
Section 24:11A-10 - Violations; penalties; recovery; disposition
Section 24:11A-11 - Separate violations
Section 24:11A-12 - Actions to restrain violations
Section 24:11A-13 - Repeal of conflicting acts; saving clause
Section 24:11A-14 - Effective date
Section 24:12-1 - "Nonalcoholic drink" defined
Section 24:12-2 - Prohibited adulterations; drinks containing water treated with fluorides
Section 24:12-4 - False advertising
Section 24:12-5 - Licensing of wholesale bottlers
Section 24:12-6 - Issuance of license; period of
Section 24:12-7 - Revocation or suspension of license
Section 24:12-9 - State regulations, standards for bottled water.
Section 24:12-10 - Periodic testing
Section 24:12-12 - Procedures, rules, regulations
Section 24:12-13 - Powers of commissioner
Section 24:12-14 - Violations; penalties
Section 24:14A-1 - Use on toys, furniture or accessible surfaces of dwelling; prohibition
Section 24:14A-3 - Violations; disorderly persons
Section 24:14A-4 - Definitions
Section 24:14A-6 - Responsibilities of board; enforcement, reports.
Section 24:14A-7 - Order for remediation, disposition of lead-based paint hazard.
Section 24:14A-8 - Notification to owner of hazard, contents.
Section 24:14A-8.1 - Eviction of occupants to avoid corrective maintenance
Section 24:14A-10 - Nonenforcement by board; enforcement by department
Section 24:14A-11 - Rules and regulations by department
Section 24:15-2 - Cleanliness, lighting, plumbing and ventilation
Section 24:15-3 - Construction of walls and floors
Section 24:15-5 - Protection of food, drugs or cosmetics from contamination; removal of refuse
Section 24:15-6 - Clothing of employees to be kept clean
Section 24:15-7 - Toilet facilities for and personal cleanliness of employees
Section 24:15-8 - Expectoration prohibited
Section 24:15-9 - Sleeping in rooms of food establishment
Section 24:15-10 - Persons affected with communicable disease
Section 24:15-11 - Order to abate violation in lieu of prosecution
Section 24:15-12 - Furnishing and posting abstract of law
Section 24:15-13 - License; necessity; fee; exemptions
Section 24:15-14 - Fee for license or inspection.
Section 24:15A-2 - Penalties; recovery and enforcement
Section 24:15A-3 - Packaging of meat
Section 24:15A-4 - Applicability of act; enforcement
Section 24:16B-1 - Short title
Section 24:16B-2 - Declaration of policy
Section 24:16B-3 - Definitions
Section 24:16B-5 - General power of the board; rules and regulations
Section 24:16B-6 - General powers of the secretary
Section 24:16B-7 - Enforcement by municipalities
Section 24:16B-10 - Powers and duties of local inspectors
Section 24:16B-17 - Inspections
Section 24:16B-18 - Disposition of dead animals
Section 24:16B-19 - Diseased or physically impaired animals
Section 24:16B-20 - Antemortem inspections
Section 24:16B-21 - Unauthorized entry of uninspected animals prohibited
Section 24:16B-22 - Separate slaughter of animals found to show symptoms of disease
Section 24:16B-23 - Separate slaughter and preparation of horsemeat
Section 24:16B-24 - Postmortem inspection
Section 24:16B-25 - Inspection mark required before processing
Section 24:16B-26 - Inspection during processing or preparation
Section 24:16B-27 - Inspection required before packaging or shipment
Section 24:16B-28 - Condemnation; disposition
Section 24:16B-29 - Disposition of by-products
Section 24:16B-30 - Actions authorized
Section 24:16B-31 - Handling, transporting and storing
Section 24:16B-33 - Contents of labels
Section 24:16B-34 - Registration of labels, marks
Section 24:16B-35 - Sale or shipment of mislabeled packages prohibited
Section 24:16B-36 - Sale or shipment of unwholesome meat prohibited
Section 24:16B-37 - Acceptance by handler-distributor of unwholesome meat prohibited
Section 24:16B-38 - Sale or shipment of horsemeat prohibited
Section 24:16B-39 - Vehicle permits
Section 24:16B-40 - Display of vehicle permits required
Section 24:16B-41 - Other applications of this act
Section 24:16B-42 - Exemption from inspection
Section 24:16B-43 - Removal of inspectors
Section 24:16B-44 - Engaging in business prohibited after removal of inspectors
Section 24:16B-45 - Acts of agents, servants and employees
Section 24:16B-46 - Books and records; rights of entry, inspection of premises
Section 24:16B-47 - Reports of licensee
Section 24:16B-48 - Proceedings before the secretary
Section 24:16B-49 - Hearing procedures
Section 24:16B-50 - Issuance of subpoenas
Section 24:16B-51 - Service of subpoenas; fees and mileage
Section 24:16B-52 - Refusal to obey subpoena or testify; contempt
Section 24:16B-54 - Grounds for denying license
Section 24:16B-55 - Informal hearings on violations; adjustment
Section 24:16B-56 - Orders of the secretary; service
Section 24:16B-57 - Records of the secretary; reports to the Attorney General
Section 24:16B-58 - Disposition of license fees, penalties, fines and costs
Section 24:16B-59 - Review by Superior Court
Section 24:16B-60 - Violations
Section 24:16B-61 - Actions to restrain violations
Section 24:16B-62 - Co-operation with United States Government
Section 24:16B-63 - Agreements with other agencies
Section 24:16B-64 - Grant of specific powers not to impair general powers
Section 24:16B-65 - Foreign or interstate commerce
Section 24:16B-67 - Authority of the division of weights and measures not abrogated or affected
Section 24:16B-68 - Liberal construction
Section 24:16B-69 - Inconsistent acts and rules and regulations superseded
Section 24:16B-70 - Partial invalidity
Section 24:17-2 - Different places or days as separate violations
Section 24:17-3 - Payment of penalty equivalent to conviction
Section 24:17-4 - Action to restrain violation
Section 24:17-5 - Recovery of penalties; enforcement
Section 24:17-8 - Disposition of penalties collected
Section 24:2I-2 - Definitions.
Section 24:21-3 - Authority to control.
Section 24:21-4 - Schedules of controlled substances
Section 24:21-6 - Schedule II.
Section 24:21-7 - Schedule III.
Section 24:21-8 - Schedule IV.
Section 24:21-8.1 - Schedule V.
Section 24:21-9 - Rules and regulations.
Section 24:21-10 - Registration requirements.
Section 24:21-11 - Registration.
Section 24:21-12 - Denial, revocation, or suspension of registration.
Section 24:21-13 - Records of registrants.
Section 24:21-14 - Order forms.
Section 24:21-15 - Prescriptions.
Section 24:21-15.3 - Rules, regulations.
Section 24:21-17 - Form of label to be used by pharmacists; altering or removing label.
Section 24:21-23 - General penalty
Section 24:21-24 - Attempt, endeavor and conspiracy
Section 24:21-25 - Additional penalties
Section 24:21-29 - Second or subsequent offenses
Section 24:21-31 - Powers of enforcement personnel.
Section 24:21-32 - Administrative inspections and warrants.
Section 24:21-33 - Injunctions
Section 24:21-34 - Cooperative arrangements.
Section 24:21-36 - Reports of convictions of manufacturers and practitioners.
Section 24:21-37 - Burden of proof; liabilities; immunity
Section 24:21-38 - Judicial review.
Section 24:21-40 - Pending proceedings
Section 24:21-42 - Uniformity of interpretation
Section 24:21-43 - Severability
Section 24:21-44 - Study of penalties relating to use and possession of marihuana
Section 24:21-52 - Seizure in violation of act
Section 24:21-53 - Severability
Section 24:21-54 - "Controlled Dangerous Substances Administration and Enforcement Fund."