Which federal agency regulates packaging, labeling, and transportation of biological products?

The federal agency responsible for regulating the packaging, labeling, and transportation of biological products is the Food and Drug Administration (FDA). The FDA’s jurisdiction includes the oversight of a wide range of products, including food, pharmaceuticals, and biologics, which encompass vaccines and other biological products. The agency establishes regulations to ensure that these products are safe, effective, and labeled appropriately for public use.

The FDA sets forth guidelines to ensure that biological products are properly handled throughout their lifecycle, from manufacturing to distribution to administration. This includes regulations on the packaging standards to prevent contamination and ensure the stability of these products during transport.

While the Department of Transportation does have authority over the transportation of hazardous materials, including certain biological materials, its role is more focused on the transportation safety aspects rather than product-specific regulations. The Environmental Protection Agency deals primarily with environmental regulations and public health related to chemical substances and pollutants, and the Occupational Safety and Health Administration focuses on workplace safety and health. These agencies do not specifically regulate the biological products in the manner that the FDA does.