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 152
... banks and working cell banks that were established using bovine - derived materials sourced from countries on the USDA list should be re - derived with bovine - derived materials from countries not on the USDA list . However , master ...
... banks and working cell banks that were established using bovine - derived materials sourced from countries on the USDA list should be re - derived with bovine - derived materials from countries not on the USDA list . However , master ...
Page 153
... banks is even more remote than that presented by the working seed banks and is outweighed by the risk of altering the bacterial or viral vaccine through re - derivation . Finally , that these issues are of public interest and ...
... banks is even more remote than that presented by the working seed banks and is outweighed by the risk of altering the bacterial or viral vaccine through re - derivation . Finally , that these issues are of public interest and ...
Page 172
... Banks prohibits pooling of tissues for its members . The FDA has issued new rules regarding tissue processing . Those rules include a prohibition on pooling tissue from multiple donors but allow for a waiver under certain circumstances ...
... Banks prohibits pooling of tissues for its members . The FDA has issued new rules regarding tissue processing . Those rules include a prohibition on pooling tissue from multiple donors but allow for a waiver under certain circumstances ...
Page 173
... banks are now required to register with the FDA . The number registering is substantially larger than the number known to exist prior to this rule . This means that a large number of facilities have been operating without any ...
... banks are now required to register with the FDA . The number registering is substantially larger than the number known to exist prior to this rule . This means that a large number of facilities have been operating without any ...
Page 428
... banks , source plasma operations and biologics manufacturing establishments . Conduct targeted BSE inspections of 100 % of all known renderers and feed mills handling prohibited material . Ensure at least 97 % of mammography facilities ...
... banks , source plasma operations and biologics manufacturing establishments . Conduct targeted BSE inspections of 100 % of all known renderers and feed mills handling prohibited material . Ensure at least 97 % of mammography facilities ...
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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...