Establishments and Products Licensed under Section 351 of the Public Health Service Act. Documentation

摘要

The document contains lists of manufacturers licensed to make and sell biological products under Section 351 of the Public Health Services Act. The licenses are regulated by the Center of Biologics Evaluation and Research (CBER) within the Food and Drug Administration (FDA). It is divided into four sections: Establishments and Locations, Establishments and Products, Biological Products and Establishments Licensed for each Product, and Alphabetical List of Biological Products by Category.