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The Space Development Agency (SDA) was established in 2019 by Mike Griffin with his appointment to Under Secretary of Defense (R&E) by President Donald Trump. [8] Griffin was a long time advocate for low Earth orbit constellations to eliminate U.S. vulnerability to ballistic missiles with his work on space-based interceptors for the Strategic Defense Initiative and Brilliant Pebbles in the 1980s.
FDA Building 51 is one of the main buildings in its White Oak campus that houses the Center for Drug Evaluation and Research. The Center for Drug Evaluation and Research (CDER, pronounced "see'-der") is a division of the U.S. Food and Drug Administration (FDA) that monitors most drugs as defined in the Food, Drug, and Cosmetic Act.
A new drug application in the 1930s for sulfapyridine to the United States Food and Drug Administration. The Food and Drug Administration's (FDA) New Drug Application (NDA) is the vehicle in the United States through which drug sponsors formally propose that the FDA approve a new pharmaceutical for sale and marketing.
The Food and Drug Administration Safety and Innovation Act of 2012 (FDASIA) is a piece of American regulatory legislation signed into law on July 9, 2012.It gives the United States Food and Drug Administration (FDA) the authority to collect user fees from the medical industry to fund reviews of innovator drugs, medical devices, generic drugs and biosimilar biologics.
The dismantling of USAID by the Trump administration means there are no staff to process waivers submitted by food and other aid organizations hoping to resume operations under humanitarian ...
An anonymous OPM staffer told the Musk Watch newsletter on Feb. 3 that the server was "a piece of commercial hardware they believed was not obtained through the proper federal procurement process."
A biologics license application (BLA) is defined by the U.S. Food and Drug Administration (FDA) as follows: The biologics license application is a request for permission to introduce, or deliver for introduction, a biologic product into interstate commerce (21 CFR 601.2). The BLA is regulated under 21 CFR 600 – 680.
It requires the FDA to establish an Office of the Chief Scientist to: (1) oversee, coordinate, and ensure quality and regulatory focus of FDA intramural research programs; (2) track and coordinate intramural research awards made by each FDA center or science-based office; (3) develop and advocate for a budget to support intramural research; (4 ...