Agriculture, Rural Development, Food and Drug Administration, and Related Agencies Appropriations for 2003: Agricultural programsU.S. Government Printing Office, 2002 - United States |
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Page 52
... regulatory issues related to cytokines , growth factors and studies on interferon purification , characterization and interferon receptors . She worked at NIH from 1975 to 1980 , with Nobel Prize Laureate Christian B. Anfinsen on the ...
... regulatory issues related to cytokines , growth factors and studies on interferon purification , characterization and interferon receptors . She worked at NIH from 1975 to 1980 , with Nobel Prize Laureate Christian B. Anfinsen on the ...
Page 53
... Regulatory Affairs Mr. Baker is responsible for the direction and coordination of the compliance activities of the FDA . He oversees the FDA field staff of over 3,000 employees in 5 regional offices , 20 district offices , 13 field ...
... Regulatory Affairs Mr. Baker is responsible for the direction and coordination of the compliance activities of the FDA . He oversees the FDA field staff of over 3,000 employees in 5 regional offices , 20 district offices , 13 field ...
Page 77
... regulatory guidance to sponsors of vaccines used to counter terrorism , including other Federal agencies such as CDC and DOD as well as industry ; accelerate emergency vaccine lot releases ; and , provide regulatory guidance to ...
... regulatory guidance to sponsors of vaccines used to counter terrorism , including other Federal agencies such as CDC and DOD as well as industry ; accelerate emergency vaccine lot releases ; and , provide regulatory guidance to ...
Page 145
... regulatory mission . The Center for Biologics Evaluation and Research , CBER , initiated a Blood Action Plan in July 1997 to increase the effectiveness of its scientific and regulatory actions , and to ensure greater coordination with ...
... regulatory mission . The Center for Biologics Evaluation and Research , CBER , initiated a Blood Action Plan in July 1997 to increase the effectiveness of its scientific and regulatory actions , and to ensure greater coordination with ...
Page 169
... regulation through regulatory changes , other concerns would have to be addressed by Congress through legislative action . The further delay is necessary to give Congress time to consider the information and conclusions contained in the ...
... regulation through regulatory changes , other concerns would have to be addressed by Congress through legislative action . The further delay is necessary to give Congress time to consider the information and conclusions contained in the ...
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Popular passages
Page 620 - October 31, 1977) provides that none of the funds appropriated or otherwise made available by this Act to the...
Page 438 - ... payment for publication of technical and Informational materials in professional and trade Journals...
Page 1193 - The four regulatory agencies that issued today's stateaents are the Office of the Comptroller of the Currency (OCC) , the Federal Deposit Insurance Corporation (FDIC), the Federal Reserve Board (FRB...
Page 1188 - Act of 1993 (GPRA) seeks to improve the effectiveness, efficiency, and accountability of federal programs by requiring federal agencies to set goals for program performance and to report on annual performance compared with the goals.
Page 21 - A standard for the design, conduct, performance, monitoring, auditing, recording, analyses, and reporting of clinical trials that provides assurance that the data and reported results are credible and accurate, and that the rights, integrity, and confidentiality of trial subjects are protected.
Page 388 - II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Page 326 - Available from National Technical Information Service, Springfield, VA 22151. ious requirements of the Environmental Protection Agency (EPA), the Nuclear Regulatory Commission (NRC), and other Federal and State agencies. The ultimate objective of these models is general prediction of the chemical concentrations to which organisms, including man, may be exposed following short or long-term releases of the chemical to the environment. Due to differences in intended uses, the models range in...
Page 306 - ... (A) officers and employees of the Food and Drug Administration, employees under contract with the Food and Drug Administration who work in facilities owned or leased for the Food and Drug Administration, advisory committees, and costs related to such officers, employees, and committees, (B) management of information, and the acquisition, maintenance, and repair of computer resources, (C) leasing, maintenance, renovation, and repair of facilities and acquisition, maintenance, and repair of fixtures,...
Page 260 - I would be happy to provide that information for the record. (The information follows...
Page 301 - Section 736 (g) (2) (B), states that fees: shall only be collected and available to defray increases in the costs of the resources allocated for the process for the review of human drug applications (including increases in such costs for an additional number of fulltime equivalent positions...