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…
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 role of credentials in the United States economy and workplace may be most visible in job postings or when individuals earn new credentials. However,…
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…
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,…
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…
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…
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…
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…
The Food and Drug Administration (FDA) has recognized ANAB as an accreditation body (AB) for the Laboratory Accreditation for Analyses of Foods (LAAF) program. This…