The Code of Federal Regulations of the United States of AmericaU.S. Government Printing Office, 2002 - Administrative law The Code of Federal Regulations is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government. |
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Page 7
... tion relating to possible product haz- ards ) required in labeling for food , drugs , devices , or cosmetics under ... tion of reasonable variations and ex- emptions for small packages from the required declaration of net quantity of ...
... tion relating to possible product haz- ards ) required in labeling for food , drugs , devices , or cosmetics under ... tion of reasonable variations and ex- emptions for small packages from the required declaration of net quantity of ...
Page 12
... tion to deliver , such sample . Upon re- ceipt of the notice , the owner or con- signee shall hold such article and not distribute it until further notice from the district director or the collector of customs of the results of ...
... tion to deliver , such sample . Upon re- ceipt of the notice , the owner or con- signee shall hold such article and not distribute it until further notice from the district director or the collector of customs of the results of ...
Page 19
... tion declared adulterated within the meaning of section 402 ( a ) of the Fed- eral Food , Drug , and Cosmetic Act shipments of vegetables or other edible food in used crates or containers that may render the contents injurious to health ...
... tion declared adulterated within the meaning of section 402 ( a ) of the Fed- eral Food , Drug , and Cosmetic Act shipments of vegetables or other edible food in used crates or containers that may render the contents injurious to health ...
Page 20
application , a new animal drug applica- tion , or in the case of a certifiable anti- biotic an antibiotic application for the drug product has been approved , a peti- tion has been filed as provided by para- graph ( f ) of this section ...
application , a new animal drug applica- tion , or in the case of a certifiable anti- biotic an antibiotic application for the drug product has been approved , a peti- tion has been filed as provided by para- graph ( f ) of this section ...
Page 22
... tion for the premarket review and reg- ulation of products that are comprised of any combination of a drug and a de- vice ; a device and a biological ; a bio- logical and a drug ; or a drug , a device and a biological . This ...
... tion for the premarket review and reg- ulation of products that are comprised of any combination of a drug and a de- vice ; a device and a biological ; a bio- logical and a drug ; or a drug , a device and a biological . This ...
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Common terms and phrases
acid action administrative record advisory committee agency amended amounts consistent animal drug approval Authority citation revised biological Canthaxanthin cation CBER CDER CDRH Center CFSAN chapter color additive D&C Color additive mixtures coloring purposes Commis conform in identity Cosmetic Act D&C Orange D&C Red D&C Yellow Deputy Direc Deputy Director determination diluents Director and Deputy Dockets Management Branch Drug Administration drug application employee Evaluation Exemption from certification FD&C Federal Acquisition Regulation Federal Food FEDERAL REGISTER filed following officials food additive Food and Drug hearing Identity and specifications issue Lead as Pb lic health listed manufacturing practice matter medical devices ment metics mixtures for coloring mixtures prepared therefrom notice paragraph participation party percent person petition premarket presiding officer procedures public disclosure quirements regulatory request Research restrictions safely salt Service sioner sory submitted Subpart tification tion tive
Popular passages
Page 325 - ... color additive" means a material which — (A) is a dye, pigment, or other substance made by a process of synthesis or similar artifice, or extracted, isolated, or otherwise derived, with or without intermediate or final change of identity, from a vegetable, animal, mineral, or other source, and...
Page 187 - Although relevant, evidence may be excluded if its probative value is substantially outweighed by the danger of unfair prejudice, confusion of the issues, or misleading the jury, or by considerations of undue delay, waste of time, or needless presentation of cumulative evidence.
Page 234 - Provided, however , that if any individual is denied any right, privilege, or benefit that he would otherwise be entitled "by Federal law, or for which he would otherwise be eligible, as a result of the maintenance of such material, such material shall be provided to such individual...
Page 289 - ... participation, a description of the procedures to be followed, and identification of any procedures which are experimental; (2) A description of any reasonably foreseeable risks or discomforts to the subject; (3) A description of any benefits to the subject or to others which may reasonably be expected from the research; (4) A disclosure of appropriate alternative procedures or courses of treatment, if any, that might be advantageous to the subject; (5) A statement describing the extent, if any,...
Page 480 - Central Intelligence Agency Chief Financial Officer, Office of Child Support Enforcement, Office of Children and Families, Administration for Civil Rights, Commission on Civil Rights, Office for Coast Guard Coast Guard (Great Lakes Pilotage) Commerce Department Census Bureau Economic Affairs, Under...
Page vii - MF, 8 am to 4 pmest or fax your order to 202-512-2250, 24 hours a day. For payment by check, write to the Superintendent of Documents, Attn: New Orders, PO Box 371954, Pittsburgh, PA 15250-7954. For GPO Customer Service call 202-512-1803. ELECTRONIC SERVICES The full text of the Code of Federal Regulations, the LSA (List of CFR Sections Affected), The United States Government Manual, the Federal Register, Public Laws, Public Papers, Weekly Compilation of Presidential Documents and the Privacy Act...
Page 237 - Administration concerning a refusal to amend a record under § 21.51(a)(2) or with another agency that provides the record to the Food and Drug Administration, the Food and Drug Administration shall in any subsequent disclosure under this subpart provide a copy of the statement of disagreement and a concise statement by the agency, if one has been prepared, of the reasons for not making the amendment(s) requested. § 21.75 Rights of legal guardians. For the purposes of this part, the parent of any...
Page 288 - ... rights, and whom to contact in the event of a research-related injury to the subject; and (8) A statement that participation is voluntary, refusal to participate will involve no penalty or loss of benefits to which the subject is otherwise entitled...
Page 408 - USP) 2.5. 5, and 10 mg contain FD&C Yellow No. 5 (tartrazine) which may cause allergic-type reactions (including bronchial asthma) in certain susceptible individuals. Although the overall incidence of FD&C Yellow No. 5 (tartrazine) sensitivity in the general population is low, it is frequently seen In patients who also have aspirin hypersensitivity.
Page 85 - advisory committee" means any committee, board, commission, council, conference, panel, task force, or other similar group, or any subcommittee or other subgroup thereof...