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,…
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…
Effective February 1, 2022, the Food and Drug Administration (FDA) has established the Laboratory Accreditation for Analyses of Foods (LAAF) program. This program focuses on…
Quality and safety of dietary supplements are of utmost importance to the consumer. These supplements are regulated by the United States Food and Drug Administration…
ANAB has been recognized as an accreditation body (AB) for the U.S. Food & Drug Administration (FDA) Accreditation Scheme for Conformity Assessment (ASCA) Pilot program…