Chapman R A, Morrison A B
Can Med Assoc J. 1966 Mar 19;94(12):609-13.
Prior to Confederation, food control legislation in Canada consisted of only a few simple laws governing the quality, grading, packing and inspection of certain staple foods. The Inland Revenue Act of 1875 provided the first real control in Canada over adulteration of liquor, foods and drugs. Since then, food legislation has evolved in scope and complexity as the industries involved have developed, as consumers have become better informed, and as scientific advances have provided a sound basis for regulations. Present regulations under the Food and Drugs Act are intended to give consumers broad protection against health hazards and fraud in the production, manufacture, labelling, packaging, advertising, and sale of foods. This principle is well illustrated by present requirements for the control of pesticide residues, chemical additives, and the addition of vitamins to foods. In today's era of rapid technological change, application of current scientific knowledge to the food industry obviously involves the possibility of hazards to health. Regulatory agencies with responsibility for food safety must, therefore, fully utilize scientific knowledge in order to reduce the risks involved to a minimum.
在联邦成立之前,加拿大的食品控制立法仅由少数几条简单法律组成,这些法律对某些主食的质量、分级、包装和检验进行管理。1875年的《国内税收法》首次对加拿大的酒类、食品和药品掺假实施了真正的管控。从那时起,随着相关行业的发展、消费者信息的增多以及科学进步为法规提供了坚实基础,食品立法在范围和复杂性方面不断演变。现行的《食品和药品法》规定旨在为消费者提供广泛保护,使其免受食品生产、制造、标签、包装、广告和销售过程中的健康危害和欺诈行为影响。目前对农药残留、化学添加剂以及食品中添加维生素的管控要求很好地体现了这一原则。在当今技术快速变革的时代,将当前科学知识应用于食品行业显然存在健康危害的可能性。因此,负责食品安全的监管机构必须充分利用科学知识,以便将相关风险降至最低。