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The Trinidad and Tobago Bureau of Standards (TTBS) the International Organization for Standards member body of Trinidad and Tobago. [1] Founded on July 8, 1974, the organization is responsible for establishing and maintaining the quality of all goods in the country, excluding medicine, food, and cosmetics, which are the responsibility of the Chemistry, Food and Drug Division of the Ministry of ...
The Caribbean Public Health Agency (CARPHA) is a regional public health agency headquartered in Trinidad and Tobago [2] which was established by CARICOM leaders in July 2011 [1] and began operation in 2013. [2]
The Food and Drugs Act (French: Loi sur les aliments et drogues) is an act of the Parliament of Canada regarding the production, import, export, transport across provinces and sale of food, drugs, contraceptive devices and cosmetics (including personal cleaning products such as soap and toothpaste). It was first passed in 1920 and most recently ...
Pure Food and Drug Act (1906) – Also known as the Wiley Act, It was passed in response to public concern about food and drug safety. Administered by the Bureau of Chemistry, it required that food be pure and wholesome and drug ingredients to be listed and prohibited interstate commerce in food, drinks, and drugs that did not meet these requirements.
Trinidad and Tobago operates under a two-tier healthcare system. That is, there is the existence of both private and public facilities. The Ministry of Health is responsible for leading the health sector. The service provision aspect of public healthcare has been devolved to newly created entities, the Regional Health Authorities (RHAs). Responsibility for the provi
The Pure Food and Drug Act of 1906 was a key piece of Progressive Era legislation, signed by President Theodore Roosevelt on the same day as the Federal Meat Inspection Act. Enforcement of the Pure Food and Drug Act was assigned to the Bureau of Chemistry in the U.S. Department of Agriculture which was renamed the U.S. Food and Drug ...
In June 1906, President Theodore Roosevelt signed into law the Pure Food and Drug Act, also known as the "Wiley Act" after its chief advocate. [1] The Act prohibited, under penalty of seizure of goods, the interstate transport of food which had been "adulterated," with that term referring to the addition of fillers of reduced "quality or strength," coloring to conceal "damage or inferiority ...
In Canada, regulation of therapeutic goods is done by Health Canada and governed by the Food and Drug Act and associated regulations. In addition, the Controlled Drugs and Substances Act specifies additional regulatory requirements for controlled drugs and drug precursors. [18]