Yes, the FDA has multiple approval pathways depending on the type of product. For instance, New Drug Applications (NDA) are required for new pharmaceuticals, while Biologics License Applications (BLA) are necessary for biologics. Cosmetics and dietary supplements are subject to different regulations, where the focus is on ensuring that they do not contain substances that can cause harm. The FDA also provides Emergency Use Authorizations (EUA) for the expedited release of products during public health emergencies, provided there is sufficient evidence to suggest the product's benefits outweigh its risks.
