Biologic Manufacturing and the FDA Essay Example | Topics and Well Written Essays - 500 words

Biologic Manufacturing and the FDA - Essay spokespersonBiologics combined with radioactive components are considered biologics, while biologics combined with non-radioactive components are drugs. While most analyses of the U.S. Food and do drugs Administration (FDA) focus on the agencys authority to decide which new treatments reach the American marketplace, the FDA plays a restrictive gatekeeper role at another key point in the biological knowledge process. In reviewing investigational new drug applications (INDs), the FDA determines which experimental therapies, vaccines, and other biological products advance from preclinical through clinical development to the licensing phase (Mark). Biopharmaceuticals are licensed under Section 351 of the Public Health Service Act (Mark)and in specific sections of the Food, Drug and Cosmetic Act. To obtain marketing approval for a new biologic, an applicant submits a biologics license application (BLA) (Koan and Ellis). The BLA must permit age ncy reviewers to make four principal determinationsThe growth media fall under Federal food, Drug and Cosmetic Act (the act) and hence, controlled by the same, specifically, if the media is derived from any protein, a label stating the misadventure of the media as an allergen should be stated.