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 182
... institutions . Medical Devices - The Secretary is urged to submit a report to the Committee on medical devices developed or improved by the Federal Government or in conjunction with Federal funds . The report should specifically address ...
... institutions . Medical Devices - The Secretary is urged to submit a report to the Committee on medical devices developed or improved by the Federal Government or in conjunction with Federal funds . The report should specifically address ...
Page 669
... institutions to augment the Agency's scientific and technological expertise , also associated with medical devices . Both of these new institutional arrangements should enable FDA to realize scientific and regulatory synergies that ...
... institutions to augment the Agency's scientific and technological expertise , also associated with medical devices . Both of these new institutional arrangements should enable FDA to realize scientific and regulatory synergies that ...
Page 794
... institutions . NCTR uses several strategies to ensure the quality of its research and the accuracy of data collected in specific research studies . Study protocols are developed collaboratively by principal investigators and FDA product ...
... institutions . NCTR uses several strategies to ensure the quality of its research and the accuracy of data collected in specific research studies . Study protocols are developed collaboratively by principal investigators and FDA product ...
Page 810
... institutions conduct their business and interact with their customers . If , in the conduct of its business , a System institution violates a law or regulation , or does not meet safety and soundness standards , we can use our ...
... institutions conduct their business and interact with their customers . If , in the conduct of its business , a System institution violates a law or regulation , or does not meet safety and soundness standards , we can use our ...
Page 812
... institutions . For example , focusing on only the most critical positions – financial examiners – the agency could lose up to 26 examiners between now and the end of FY 2005. Specifically , we could lose 12 examiners in 2002 ; 6 ...
... institutions . For example , focusing on only the most critical positions – financial examiners – the agency could lose up to 26 examiners between now and the end of FY 2005. Specifically , we could lose 12 examiners in 2002 ; 6 ...
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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...