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, Del 3U.S. Government Printing Office, 1985 |
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Side 346
... antibody XMME - 001 - DTPA- IIIIN Trade - Same as generic Generic - antimelanoma antibody XMMME - 001 - RTA Trade - Same as generic Generic - antithrombin III ( AT - 1 ) Trade - Not established Generic - botulinum A toxin Trade ...
... antibody XMME - 001 - DTPA- IIIIN Trade - Same as generic Generic - antimelanoma antibody XMMME - 001 - RTA Trade - Same as generic Generic - antithrombin III ( AT - 1 ) Trade - Not established Generic - botulinum A toxin Trade ...
Side 372
... antibodies ; studies to understand the host - parasite relationship in pertussis , develop vaccines , and develop more specific and sensitive animal tests for determination of pertussis potency and freedom from tox- icity ; studies on ...
... antibodies ; studies to understand the host - parasite relationship in pertussis , develop vaccines , and develop more specific and sensitive animal tests for determination of pertussis potency and freedom from tox- icity ; studies on ...
Side 399
... antibodies for use against pre - determined antigens . The fusion of a transformed cell with one capable of secreting a single antibody type , thereby conferring immortality and monospecificity on the daughter clones , enables ...
... antibodies for use against pre - determined antigens . The fusion of a transformed cell with one capable of secreting a single antibody type , thereby conferring immortality and monospecificity on the daughter clones , enables ...
Side 400
... antibodies are used in pathology to detect malig- nant cells in tissue sections . Most therapeutic uses for monoclonal antibodies have been for cancer patients . These include attempts at therapy of almost every malignant cell type with ...
... antibodies are used in pathology to detect malig- nant cells in tissue sections . Most therapeutic uses for monoclonal antibodies have been for cancer patients . These include attempts at therapy of almost every malignant cell type with ...
Side 432
... antibody test kits and to the evalua- tion of the safety of blood products . Studies are being conducted to better define the conditions under which heat applied during the preparation of Factor VIII and IX Concentrates and other blood ...
... antibody test kits and to the evalua- tion of the safety of blood products . Studies are being conducted to better define the conditions under which heat applied during the preparation of Factor VIII and IX Concentrates and other blood ...
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Vanlige uttrykk og setninger
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
Populære avsnitt
Side 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...
Side 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...
Side 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.
Side 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.
Side 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...
Side 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...
Side 94 - Commission be modified or set aside in whole or in part. A copy of...
Side 91 - Service may be made by leaving a copy of the process in the office of the...
Side 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...
Side 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...