Agriculture, rural development, and related agencies appropriations for 1986: hearings before a subcommittee of the Committee on Appropriations, House of Representatives, Ninety-ninth Congress, first session, Parte3U.S. Government Printing Office, 1985 |
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Página 287
... Blood and Blood Products ....... Viral & Rickettsial Products ... Bacterial & Allergenic Products Health Fraud ... Total Human Drugs and Biologics 184 9,245 2.6 2.3 201 15,518 2.9 3.8 199 12,239 2.9 3.0 103 7,098 1.4 1.8 120 10,887 1.7 ...
... Blood and Blood Products ....... Viral & Rickettsial Products ... Bacterial & Allergenic Products Health Fraud ... Total Human Drugs and Biologics 184 9,245 2.6 2.3 201 15,518 2.9 3.8 199 12,239 2.9 3.0 103 7,098 1.4 1.8 120 10,887 1.7 ...
Página 290
... Blood and Blood Products ..... Viral and Rickettsial Products . Health Fraud : Human Drugs and Biologics ...... ANIMAL DRUGS AND FEEDS PROJECT MANAGER Pasquale Lombardo Gerad L. McCowin John E. Vanderveen , Ph.D. Ralston B. Read , Jr ...
... Blood and Blood Products ..... Viral and Rickettsial Products . Health Fraud : Human Drugs and Biologics ...... ANIMAL DRUGS AND FEEDS PROJECT MANAGER Pasquale Lombardo Gerad L. McCowin John E. Vanderveen , Ph.D. Ralston B. Read , Jr ...
Página 296
... Blood and Blood Products ; Viral and Rickettsial Products : These projects provide scientific and medical support to dispute claims made for health fraud products . Over - the - Counter Drug Evaluation : This project provides ...
... Blood and Blood Products ; Viral and Rickettsial Products : These projects provide scientific and medical support to dispute claims made for health fraud products . Over - the - Counter Drug Evaluation : This project provides ...
Página 313
... blood pressure , stroke , or both , the Agency be- lieves that additional studies are necessary to determine if this drug can be generally recognized as safe and effective for OTC use . Manufacturers have agreed to conduct additional ...
... blood pressure , stroke , or both , the Agency be- lieves that additional studies are necessary to determine if this drug can be generally recognized as safe and effective for OTC use . Manufacturers have agreed to conduct additional ...
Página 361
... Blood Institute , and the National Institute of Allergy and Infectious Diseases , report on their research efforts to pinpoint the cause and to find a treatment for this disease , which has almost reached epidemic proportions among ...
... Blood Institute , and the National Institute of Allergy and Infectious Diseases , report on their research efforts to pinpoint the cause and to find a treatment for this disease , which has almost reached epidemic proportions among ...
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Términos y frases comunes
Act 21 USC action addition Agency amended antibody antibody test approved audit blood Center CFTC clinical Commission's Committee Commodity Exchange Act Commodity Futures Trading commodity pool compliance conducted contract market Cosmetic Act 21 costs CPOs Delaney Clause Director Division donors Drug Administration drug applications effective enforcement evaluation Federal Food fees filed fiscal year 1984 Food and Drug funds futures contracts Futures Trading Commission HTLV HTLV-III antibody implement increase investigations issued labeling leverage transaction listed drug Market Surveillance Methyl Bromide monitoring National Futures Association NFA's NPRM Office orphan drugs orphan products patent percent person personnel PHILLIPS plasma proposed rare diseases recommendations reduced registration regulations regulatory request responsibility result rules safety Services staff staff-years studies submitted subsection Tegretol tion treatment virus Western blot WHITTEN
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Página 81 - The act, omission, or failure of any official, agent, or other person acting for any individual, association, partnership, corporation, or trust within the scope of his employment or office shall be deemed the act, omission, or failure of such individual, association, partnership, corporation, or trust, as well as of such official, agent, or other person. The words "interstate commerce...
Página 592 - Secretary (A) fails to establish that the proposed use of the food additive under the conditions of use to be specified in the regulation will be safe: provided that no additive shall be deemed to be safe if it is found to induce cancer when ingested by man or animal or if it is found, after tests which are appropriate for the evaluation of the safety of food additives, to induce cancer in man or animal...
Página 83 - For the purpose of any such investigation, or any other proceeding under this title, any member of the Commission or any officer designated by it is empowered to administer oaths and affirmations, subpoena witnesses, compel their attendance, take evidence, and require the production of any books, papers, correspondence, memoranda, or other records which the Commission deems relevant or material to the inquiry.
Página 592 - ... that no residue of the additive will be found (by methods of examination prescribed or approved by the Secretary by regulations, which regulations shall not be subject to subsections (f) and (g)) in any edible portion of such animal after slaughter or in any food yielded by or derived from the living animal- or SBC.
Página 95 - Code. (2) If the petitioner applies to the court for leave to adduce additional evidence, and shows to the satisfaction of the court that such additional evidence is material and that there were reasonable grounds...
Página 322 - Secretary pursuant to subsection (b), do not include adequate tests by all methods reasonably applicable to show whether or not such drug is safe for use under the conditions prescribed, recommended, or suggested in the proposed labeling...
Página 94 - Commission be modified or set aside in whole or in part. A copy of...
Página 91 - Service may be made by leaving a copy of the process in the office of the...
Página 83 - The Commission may, in its discretion, make such investigations as it deems necessary to determine whether any person has violated or is about to violate...
Página 101 - ... or any rule or regulation thereunder or any undertaking contained in a registration statement as provided in subsection (d) of Section 15 of this title, which statement was at the time and in the light of the circumstances under which it was made false or misleading with respect to any material fact...