This chapter examines the importance of safety measures in healthcare and food products, emphasizing the risks associated with unsafe additives, contamination, and improper handling. It highlights the roles of regulatory frameworks established by critical organizations such as the World Health Organization (WHO) and the U.S. Food and Drug Administration (FDA) in maintaining rigorous safety standards. The chapter also explores how environmental factors, including temperature and moisture, affect product stability and quality, thereby influencing health outcomes. A significant focus is placed on the ethical responsibilities of businesses to prioritize consumer health over profit, advocating for transparency and compliance with safety guidelines. The discussion underscores the necessity of implementing robust quality controls, utilizing up-to-date manufacturing equipment, and adhering to proper storage practices to minimize health risks. By arguing for a comprehensive ethical and regulatory approach, the chapter seeks to ensure the safety and well-being of consumers, ultimately reinforcing the critical intersection of public health, regulatory compliance, and ethical manufacturing practices.
Author
(s) Details
Sivakumar
J T Gowder
College of Applied Medical Sciences, King Faisal University,
Hufuf, KSA.
Please see the book here:- https://doi.org/10.9734/bpi/dhrni/v10/3016
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