Canadian Food and Drugs Act definition

Canadian Food and Drugs Act means the statute of Canada cited as R.S.C. 1985, c. F-27 and regulations thereto, as amended from time to time;
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Examples of Canadian Food and Drugs Act in a sentence

  • For Products that are food related products, including the contents, packaging, and labeling, Applicable Laws shall also include but not be limited to the Federal Food, Drug, and Cosmetic Act of 1938, the Canadian Food and Drugs Act and its Regulations, the Fair Packaging and Labeling Act, the Consumer Packaging and Labelling Act, and the Food Safety Modernization Act, as applicable.

  • For geographical areas where there are no regulatory laws for such substances, eligibility will be determined by Canadian standards as defined by the Canadian Food and Drugs Act and Regulations.

  • MEC warrants that all Products, all food additives in the Products, and all substances for use in, with, or for the Products, comprising each shipment or other delivery hereby made by MEC to, or on the order of, Distributor are hereby guaranteed as of the date of such shipment to be, on such date, not adulterated or mislabeled in accordance with the Canadian Food and Drugs Act and the Natural Health Products Regulations promulgated thereunder.

  • HQ agrees that all Plasma it collects in Canada for pickup by Supplier for fractionation by Supplier shall be collected, stored and transported in accordance with the Canadian Food and Drugs Act and the Drugs Directorate Guidelines on Blood Collection and Blood Component Manufacturing, 1992, established plasma specifications, and any amendments thereto, and in accordance with current import/export regulations.

  • Unlike the United States, Canada has two official languages: English and French.115 The Canadian Food and Drugs Act regulates the labeling of Food, Drugs, and Cosmetics.

  • CBS agrees that all Plasma it collects in Canada for pickup by Supplier for fractionation by Supplier shall be collected, stored and transported in accordance with the Canadian Food and Drugs Act and the Drugs Directorate Guidelines on Blood Collection and Blood Component Manufacturing, 1992, established plasma specifications, and any amendments thereto, and in accordance with current import/export regulations.

  • Similarly, India’s uranium supplies to meet its nuclear energy aspirations is also expected to fall short of its requirements.High Transmission and Distribution losses and slow rate of DISCOM reforms are likely to hurt the industry in the last mile.

  • The Canadian Food and Drugs Act - C.05.005 (e) describes the requirement for a sponsor to file the IB as part of their REB application; however underC.05.012 (d) (g) it is not included in the documents that the FHREB must approve.

  • For over 10 years sodium nitrite was a permitted preservative for fresh fish under the Canadian Food and Drugs Act, and it was not until 1959 that these regulations were amended so that nitrites were no longer on the list of additives permitted for inclusion in fish products.

  • Drug and Cosmetic Act, as amended, including the Food Additives Amendment of 1958 (the “Act”), or within the meaning of any substantially identical and applicable state food and drug law, if any, and not articles which may not under the provisions of Sections 404, 505, or 512 of the Act, be introduced into interstate commerce, the Canadian Food and Drugs Act, and the Natural Health Product Regulations promulgated thereunder.

Related to Canadian Food and Drugs Act

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

  • Food and food ingredients means substances, whether in liquid, concentrated, solid, frozen, dried, or dehydrated form, that are sold for ingestion or chewing by humans and are consumed for their taste or nutritional value. Food and food ingredients do not include alcoholic beverages and tobacco.

  • Foreign Financial Regulatory Authority shall have the meaning given by Section 2(a)(50) of the 0000 Xxx.

  • Foreign Corrupt Practices Act means the Foreign Corrupt Practices Act of the United States, 15 U.S.C. Sections 78a, 78m, 78dd-1, 78dd-2, 78dd-3, and 78ff, as amended, if applicable, or any similar law of the jurisdiction where the Property is located or where the Company or any of its Subsidiaries transacts business or any other jurisdiction, if applicable.

  • FFDCA means the United States Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 301 et seq., as amended from time to time, together with any rules, regulations and requirements promulgated thereunder (including all additions, supplements, extensions, and modifications thereto).

  • Food Security Act means the Food Security Act of 1985, 7 U.S.C. §1631, as amended, and the regulations promulgated thereunder.

  • FD&C Act means the United States Federal Food, Drug and Cosmetic Act, as amended.

  • Canadian Securities Regulatory Authorities means the securities regulatory authorities in each of the provinces and territories of Canada;

  • UK Bribery Act means the Xxxxxxx Xxx 0000 of the United Kingdom, as amended, and the rules and regulations thereunder.

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

  • Criminal drug statute means a Federal or non-Federal criminal statute involving the manufacture, distribution, dispensing, possession or use of any controlled substance.

  • Legend drugs means any drugs which are required by state

  • Applicable Canadian Securities Laws means, collectively, and as the context may require, the applicable securities legislation of each of the provinces and territories of Canada, and the rules, regulations, instruments, orders and policies published and/or promulgated thereunder, as such may be amended from time to time prior to the Effective Date;

  • New Drug Application means a new drug application in the United States for authorization to market a product, as defined in the applicable laws and regulations and submitted to the FDA.

  • Corrupt practices means the offering, giving, receiving or soliciting of anything of value to influence the action of a Government official in procurement process or in contract execution: and

  • Bribery Act means the Bribery Act 2010 and any subordinate legislation made under that Act from time to time together with any guidance or codes of practice issued by the relevant government department concerning this legislation;

  • Cannabis Act means An Act respecting cannabis and to amend the Controlled Drugs and Substances Act, the Criminal Code and other Acts, S.C. 2018, c. 16, as amended from time to time.

  • Legend drug or "prescription drug" means any drug or device that has been determined to be unsafe for self- medication or any drug or device that bears or is required to bear the legend:

  • Customs territory of the United States means the 50 States, the District of Columbia, and Puerto Rico.

  • Foreign Assets Control Regulations has the meaning set forth in Section 10.18.

  • ACNC Act means the Australian Charities and Not-for-profits Commission Act 2012 (Cth).

  • foreign regulatory authority means a securities commission, exchange or other securities market regulatory authority in a designated foreign jurisdiction;

  • Corrupt Act means any offence in respect of corruption or corrupt activities contemplated in the Prevention and Combating of Corrupt Activities Act No. 12 of 2004;

  • corrupt practice means the offering, giving, receiving, or soliciting of anything of value to influence the action of a public official in the procurement process or in contract execution.

  • United States Bankruptcy Code means the Bankruptcy Reform Act of 1978, as amended and as codified in Title 11 of the United States Code, as amended from time to time hereafter, or any successor federal bankruptcy law.

  • Federal Aviation Act means subtitle VII of Title 49 of the United States Code, or any successor provision.