Food and Drug Act definition

Food and Drug Act means the Federal Food, Drug and Cosmetic Act, as amended, 21 U.S.C. § 301 et seq. and any successor act.
Sample 1Sample 2Sample 3
Food and Drug Act means the Food, Drug and Cosmetic Act, 21 U.S.C. 301-391.
Sample 1Sample 2
Food and Drug Act has the meaning set forth in Section 3.18 (Products).
Sample 1Sample 2

Examples of Food and Drug Act in a sentence

  • In addition, Client shall indemnify and hold harmless the Catalent Indemnitees from and against any and all Losses arising out of or resulting from any federal regulatory filings by or on behalf of Client or any of its Affiliates, including Losses incurred by Catalent arising from filings under 21 U.S.C. 355 and/or Section 505 of the Food and Drug Act (or non-U.S. equivalents) and related claims or proceedings (including Losses associated with Catalent’s obligation to respond to third party subpoenas).

  • All meat and meat products sold must comply with all aspects of the Federal Food and Drug Act of June 30, 1906 and all amendments thereto; and to subsequent decisions of the United States Department of Agriculture applicable thereto.

  • It is unclear why the court views the enforcement protocol as any different from EPA’s announcement that it would no longer consider human studies in enforcing FIFRA and the Food and Drug Act, see Croplife, 329 F.3d at 878-79.

  • Non-Renewal of Administrator Contract Soto, Nancy A., Project Director, Career Transition Services (2ASP11)(The position is grant-funded by the Alameda County Workforce Investment Board, and therefore subject to annual renewal.

  • At the Federal level, these efforts go back to the Pure Food and Drug Act of 1906, the United States’ first national food safety law.

  • That I have been arrested or charged with an offence under The Criminal Code of Canada, The Narcotic Control Act, The Food and Drug Act, The Securities Act of any Province of Canada, or any legislation similar to any of the foregoing in any other jurisdiction, or have been a defendant in a civil action relating to fraud; YesNo 8.

  • Sinclair’s work is credited with aiding passage of the Pure Food and Drug Act and Meat Inspection Act, both enacted in 1906, which instituted vigorous reforms in the meatpacking industry.

  • That I have been arrested or charged on any offence under The Criminal Code of Canada, The Narcotic Control Act, The Food and Drug Act, The Securities Act of any Province of Canada, or any legislation similar to any of the foregoing in any other jurisdiction, or have been a defendant in a civil action relating to fraud;Yes Yes YesNo 5.

  • It can also contribute to reduced energy costs, depending on the size of the system installed.JohnstonCounty SchoolsUse 25 Percent LessEnergy In the 1990s,JohnstonCounty in NorthCarolina built two daylit middleschools using an extensivesouth-facing roof monitor strategy.

  • Drugs and medicines which are dispensed by a licensed pharmacist require the written prescription of a doctor or dentist according to the Food and Drug Act and according to Canadian or provincial legislation in effect where the drug is dispensed.


More Definitions of Food and Drug Act

Food and Drug Act means the United States Federal Food, Drug, and Cosmetics Act, and all regulations, directives, policy statements and guidelines promulgated thereunder or issued pursuant thereto, as the same may be amended, modified or replaced from time to time.
Sample 1
Food and Drug Act means Food and Drug Act (Canada). “Green House” means Green House Holdings North America Inc.
Sample 1
Food and Drug Act is defined in Section 4.11(c).
Sample 1
Food and Drug Act means the Federal Food, Drug, and Cosmetic Act (21 U.S.C. § 301 et seq.). “GAAP” shall mean United States generally accepted accounting principles.
Sample 1
Food and Drug Act means the Food and Drugs Act (Canada);
Sample 1
Food and Drug Act means the Food, Drug and Cosmetic Act, 21 U.S.C. ' 301-391. "FDA" shall mean the United States Food and Drug Administration (U.S.A).
Sample 1

Related to Food and Drug Act

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

  • 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.

  • 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).

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

  • Drug abuse means any pattern of pathological use of drugs that causes impairment in social or occupational functioning, or that produces physiological dependency evidenced by physical tolerance or by physical symptoms when it is withdrawn.

  • 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.

  • Drug addiction means a disease characterized by a

  • 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:

  • Legend drugs means any drugs which are required by state

  • FDA means the United States Food and Drug Administration and any successor agency thereto.

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

  • Drug Application means a new drug application, an abbreviated drug application, or a product license application for any Product, as appropriate, as those terms are defined in the FDCA.

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

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

  • MHLW means the Japanese Ministry of Health, Labour and Welfare, and any successor agency thereto.

  • New drug means: (i) any drug, except a new animal drug or an animal feed bearing or containing

  • Prescription drug order means an original or new order from a practitioner for drugs, drug-related devices or treatment for a human or animal, including orders issued through collaborative care agreements. Lawful prescriptions result from a valid practitioner-patient relationship, are intended to address a legitimate medical need, and fall within the prescribing practitioner's scope of professional practice;

  • Invalid Drug Test means the result of a drug test for an oral fluid specimen that contains an unidentified adulterant, or an unidentified substance, that has abnormal physical characteristics, or that has an endogenous substance at an abnormal concentration preventing the laboratory from completing or obtaining a valid drug test result.

  • Covered drug means any prescription drug that:

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

  • Act of 1997 means the Taxes Consolidation Act 1997;

  • Health Canada means the section of the Canadian Government known as Health Canada and includes, among other departments, the Therapeutic Products Directorate and the Health Products and Food Branch Inspectorate;

  • Public health authority means an agency or authority of the United States, a state, a territory, a political subdivision of a state or territory, an Indian tribe, or a foreign government, or a person or entity acting under a grant of authority from or contract with such public agency, including the employees or agents of such public agency or its contractors or persons or entities to whom it has granted authority, that is responsible for public health matters as part of its official mandate.

  • Legal drug means any drug, including any prescription drug or over-the-counter drug, that has been legally obtained and that is not unlawfully sold or distributed.

  • Drug Approval Application means an application for Regulatory Approval required before commercial sale of a Product as a pharmaceutical product in a regulatory jurisdiction.

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