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 16
... inspection efforts to prevent BSE from entering or taking hold in the U.S. This plan lays out a course of action to expand our understanding of the underlying science of TSE and their ... inspections and for collection of better 12 16.
... inspection efforts to prevent BSE from entering or taking hold in the U.S. This plan lays out a course of action to expand our understanding of the underlying science of TSE and their ... inspections and for collection of better 12 16.
Page 17
... inspections and for collection of better data from both FDA & FDA State - Contract inspectors . By the end of FY 2001 we had inspected over 12,000 firms since 1997 for compliance with our BSE related feed regulations . In terms of our ...
... inspections and for collection of better data from both FDA & FDA State - Contract inspectors . By the end of FY 2001 we had inspected over 12,000 firms since 1997 for compliance with our BSE related feed regulations . In terms of our ...
Page 86
... inspection . The second thing we have done is we have increased dramati- cally the number of inspections that are going on in the field do- mestically . We are now inspecting 100 percent of all establishments that handle these ...
... inspection . The second thing we have done is we have increased dramati- cally the number of inspections that are going on in the field do- mestically . We are now inspecting 100 percent of all establishments that handle these ...
Page 87
... inspections . They are lo- cated in places that are remote from our district offices . So it is very important we have people who can get out to these remote areas of the State and inspect their facilities . We are doing a lot more ...
... inspections . They are lo- cated in places that are remote from our district offices . So it is very important we have people who can get out to these remote areas of the State and inspect their facilities . We are doing a lot more ...
Page 149
... inspections as well as a new BSE inspection checklist to better target firms for re - inspections and for collection of better data from both FDA & State inspectors . CVM also conducted two training sessions for Federal and State ...
... inspections as well as a new BSE inspection checklist to better target firms for re - inspections and for collection of better data from both FDA & State inspectors . CVM also conducted two training sessions for Federal and State ...
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90 percent act on 90 activities additional adverse events Agency Agency's Animal Drugs antimicrobial appropriate approved assessment associated bioterrorism blood Bonilla Bovine Spongiform Encephalopathy breast implant budget CFSAN clinical Committee compliance conduct consumers contamination costs Counter Terrorism CRAWFORD database dietary supplements disease domestic drug applications Drugs and Feeds electronic ensure establishments Estimate evaluate facilities Farm Credit Farm Credit System FDA's Federal fiscal Food and Drug food safety foodborne illness funding guidance HACCP Human Drugs implementation import increase industry inspections issues KAPTUR labeling laboratory Listeria monocytogenes loans mammography manufacturing medical devices medical products million monitoring MQSA Office pathogens patients PDUFA pediatric percent FY Performance Goals premarket proposed protect public health regulations regulatory request requirements Response Review and act risk Salmonella standards submissions surveillance System terrorist Undeclared color User Fees vaccines
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...