How Did Tobacco Influence US Junk Food?
Due to growing government regulation, in the mid-20th century, tobacco companies began diversifying into food manufacturing and applied similar aggressive marketing and lobbying tactics in…
ISO 22716:2007— Manufacturing Practices for Cosmetics
In the United States, the FDA regulates cosmetics under the Federal Food, Drug, and Cosmetic Act (FD&C Act). The FDA, however, does not require pre-market…
The Importance of Quality Credentials in Supporting Public Health in Food Safety
The role of credentials in the United States economy and workplace may be most visible in job postings or when individuals earn new credentials. However,…
NSF/ANSI 173:2024— Dietary Supplements
The average American diet leaves a lot of room for nutrients: 32% of our calories comes from animal foods, 57% from processed plant foods, and…
ISO 16128-1:2016—Cosmetic Ingredients And Products
Over the centuries, a pivotal and notable transformation in the beauty industry is that we have eliminated potentially deadly and dangerous chemicals (parabens, mercury, phthalates,…
ANSI/PDA Standard 001-2020: Medical Purchasing Controls
Concerns related to the efficacy and safety of medical drugs have caused most governments to develop regulatory agencies to oversee development and marketing of drug products and…
Foodborne Illness Risk Factors in Restaurants
The FDA released a report on the Occurrence of Foodborne Illness Risk Factors in Fast Food and Full-Service Restaurants. The report shows that having a…
Laboratory Requirements for the FDA LAAF Accreditation Program
What Is the FDA LAAF-Accreditation Program? Under the Federal Food, Drug and Cosmetic Act (FD&C Act), the Food and Drug Administration (FDA) has established the…
21 CFR Part 58: GLP for Nonclinical Laboratories
What Is 21 CFR Part 58? 21 CFR Part 58, Good Laboratory Practices for Nonclinical Laboratory Studies, prescribes good laboratory practices, or GLP, for conducting…