Controlled Drugs and Substances Act definition

Controlled Drugs and Substances Act means the Controlled Drugs and Substances Act, S.C. 1996, c. 19, as amended, or any successor legislation;
Controlled Drugs and Substances Act means the Controlled Drugs and Substances Act, S.C. 1996, c. 19 as amended or replaced.
Controlled Drugs and Substances Act means the Controlled Drugs and Substances Act, S.C., 1996, c.19; and

Examples of Controlled Drugs and Substances Act in a sentence

  • The Company's operations comprise a single reporting operating segment engaged in the production and sale of medical cannabis in accordance with Health Canada’s Access to Cannabis for Medical Purposes Regulation (the “ACMPR”), issued pursuant to the Controlled Drugs and Substances Act (Canada).

  • Cultivating illegal substances, as identified in the Schedule of the Controlled Drugs and Substances Act Narcotic Control Regulations, is an illegal and destructive activity.

  • For the purposes of this paragraph, a “criminal offence” includes, without being limited to, an offence under the Criminal Code (Canada), the Controlled Drugs and Substances Act (Canada) and the Food and Drugs Act (Canada).

  • Yes Noof an offence under sections 5, 6 or 7 of the Controlled Drugs and Substances Act (S.C. 1996, c.

  • FSD and FV Pharma are in the business of the production and sale of medical cannabis in accordance with Health Canada’s Access to Cannabis for Medical Purposes Regulation (the “ACMPR”), issued pursuant to the Controlled Drugs and Substances Act (Canada).

  • Machinery and equipment, “dwellings”, “buildings” and/or structures, and their contents, used in whole or in part for the cultivation, harvesting, processing, manufacture, distribution or sale of marijuana or any product derived from, or containing, marijuana or any other substance falling within the Schedules of the Controlled Drugs and Substances Act, whether or not ”you” are aware of such use of the property.

  • Deborah McGrady discusses the image of the Three Virtues appearing before Christine at her study table and then of Christine and Reason engaged in building the City of Ladies asbeing representative of modes of secular and monastic reading: “lectio to meditatio” in the first half of the illumination and movement “between operatio and contemplatio” in the portion of the image showing construction.

  • Any delays in obtaining, or failure to obtain regulatory approvals would significantly delay the development of markets and products and could have a material adverse effect on the business, results of operations and financial condition of the Issuer.Psilocybin is currently a Schedule III drug under the Controlled Drugs and Substances Act (Canada) (the “CDSA”) and it is a criminal offence to possess substances under the CDSA without a prescription or authorization.

  • Industrial Hemp Regulations (SOR/98-156), as part of the Controlled Drugs and Substances Act.

  • Regulatory Risks and Uncertainties In Canada, certain psychedelic drugs are classified as Schedule III drugs under the Controlled Drugs and Substances Act and as such, medical and recreational use is illegal under Canadian federal laws.


More Definitions of Controlled Drugs and Substances Act

Controlled Drugs and Substances Act means the Controlled Drugs and Substances Act,
Controlled Drugs and Substances Act means the Controlled Drugs and Substances Act, Canada (1996 c. 19) as amended or replaced from time to time;

Related to Controlled Drugs and Substances Act

  • Controlled Substances Act means the Controlled Substances Act (21 U.S.C. Sections 801 et seq.), as amended from time to time, and any successor statute.

  • Controlled substances means those substances identified in 49 CFR 40.85. “CCF” means the Federal Drug Testing Custody and Control Form.

  • FFDCA means the United States Federal Food, Drug, and Cosmetic Act, as amended from time to time, together with any rules, regulations and requirements promulgated thereunder (including all additions, supplements, extensions and modifications thereto).

  • Controlled substance means a controlled substance in schedules I through V of Section 202 of the Controlled Substances Act (2l U.S.C. 8l2) and as further defined in regulation at 2l CFR l308.ll-l308.l5.

  • Occupational Safety and Health Law means any Legal Requirement designed to provide safe and healthful working conditions and to reduce occupational safety and health hazards, including the Occupational Safety and Health Act, and any program, whether governmental or private (such as those promulgated or sponsored by industry associations and insurance companies), designed to provide safe and healthful working conditions.

  • FDA Act means the U.S. Federal Food, Drug and Cosmetic Act, as amended, and the rules and regulations promulgated thereunder.

  • Occupational Health and Safety Act means the Occupational Health and Safety Act, 1993 (Act No 85 of 1993);

  • Loss Absorption Regulations means, at any time, the laws, regulations, requirements, guidelines, rules, standards and policies relating to minimum requirements for own funds and eligible liabilities and/or loss absorbing capacity instruments of the United Kingdom, the PRA, the United Kingdom resolution authority, the Financial Stability Board and/or of the European Parliament or of the Council of the European Union then in effect in the United Kingdom including, without limitation to the generality of the foregoing, any delegated or implementing acts (such as regulatory technical standards) adopted by the European Commission and any regulations, requirements, guidelines, rules, standards and policies relating to minimum requirements for own funds and eligible liabilities and/or loss absorbing capacity instruments adopted by the PRA and/or the United Kingdom resolution authority from time to time (whether or not such regulations, requirements, guidelines, rules, standards or policies are applied generally or specifically to the Company or to the Regulatory Group).

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

  • Environmental, Health, and Safety Requirements means all federal, state, local and foreign statutes, regulations, ordinances and other provisions having the force or effect of law, all judicial and administrative orders and determinations, all contractual obligations and all common law concerning public health and safety, worker health and safety, and pollution or protection of the environment, including without limitation all those relating to the presence, use, production, generation, handling, transportation, treatment, storage, disposal, distribution, labeling, testing, processing, discharge, release, threatened release, control, or cleanup of any hazardous materials, substances or wastes, chemical substances or mixtures, pesticides, pollutants, contaminants, toxic chemicals, petroleum products or byproducts, asbestos, polychlorinated biphenyls, noise or radiation, each as amended and as now or hereafter in effect.

  • FDCA shall have the meaning ascribed to such term in Section 3.1(hh).

  • FD&C Act means the United States Federal Food, Drug and Cosmetic Act, as may be amended from time to time.

  • TSCA means the Toxic Substances Control Act, as amended.

  • Dangerous drug means any of the following:

  • HITECH Act means the Health Information Technology for Economic and Clinical Health Act, TitleXIII, Subtitle D, Part 1 & 2 of the American Recovery and Reinvestment Act of 2009.

  • Controlled dangerous substance means a drug, substance, or