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 1
... blood , and food from seafood to salsa . FDA is represented today by its new Deputy Commissioner Lester Crawford and his colleagues Murray Lumpkin , deputy to Dr. Crawford , and Jeff Weber , the acting CFO . In the audience , we also ...
... blood , and food from seafood to salsa . FDA is represented today by its new Deputy Commissioner Lester Crawford and his colleagues Murray Lumpkin , deputy to Dr. Crawford , and Jeff Weber , the acting CFO . In the audience , we also ...
Page 2
... blood for transfusion and blood products , tissues for transplantation , medical devices and devices that emit radi- ation , cosmetics and all feed and drugs for animals . Today our Agency is responsible for the safety , or safety and ...
... blood for transfusion and blood products , tissues for transplantation , medical devices and devices that emit radi- ation , cosmetics and all feed and drugs for animals . Today our Agency is responsible for the safety , or safety and ...
Page 11
... blood supply , drugs , and vaccines ) from contamination and tampering and shifted resources to ensure the availability of medical products necessary for public health preparedness and for use against anthrax and other biological ...
... blood supply , drugs , and vaccines ) from contamination and tampering and shifted resources to ensure the availability of medical products necessary for public health preparedness and for use against anthrax and other biological ...
Page 19
... blood screening . The research behind this advance depends on two disciplines - proteomics and computer intelligence . The diagnostic test relies on software that can detect patterns of key proteins in the blood . Using a sophisticated ...
... blood screening . The research behind this advance depends on two disciplines - proteomics and computer intelligence . The diagnostic test relies on software that can detect patterns of key proteins in the blood . Using a sophisticated ...
Page 20
... blood along with enzymes to produce the information needed for a reliable laboratory diagnosis . Generic Drugs Generic drugs provide Americans with safe and effective lower - cost alternatives to brand name prescription drugs . The ...
... blood along with enzymes to produce the information needed for a reliable laboratory diagnosis . Generic Drugs Generic drugs provide Americans with safe and effective lower - cost alternatives to brand name prescription drugs . The ...
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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...