Code of Federal Regulations: Containing a Codification of Documents of General Applicability and Future Effect as of December 31, 1948, with Ancillaries and IndexDivision of the Federal Register, the National Archives, 2002 - Administrative law Special edition of the Federal Register, containing a codification of documents of general applicability and future effect ... with ancillaries. |
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Page 7
... tion of reasonable variations and ex- emptions for small packages from the required declaration of net quantity of contents . Section 403 ( i ) of the act pro- vides for the establishment by regula- tion of exemptions from the required ...
... tion of reasonable variations and ex- emptions for small packages from the required declaration of net quantity of contents . Section 403 ( i ) of the act pro- vides for the establishment by regula- tion of exemptions from the required ...
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
... 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 , and paragraph ( e ) of this section ...
... 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 , and paragraph ( e ) 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 Act Record System action Adminis administrative record advisory committee agency amended amounts consistent animal drug approval available for public batches CBER CDER CDRH CFSAN chapter chlorofluorocarbon cluding Color additive mixtures coloring purposes Commis conform Cosmetic Act D&C Red decision Deputy Direc Deputy Director determination diluents Director and Deputy ditive Division Dockets Management Branch Drug Administration drug applications electronic employee Exemption from certification FD&C Federal Food FEDERAL REGISTER filed following officials food additive Food and Drug functions further redelegate guidance document hearing Identity and specifications investigation issue ized Labeling listed manufacturing practice matter medical devices ment metic mittee notice Office of Compliance officials are author OHIP paragraph participation party percent person petition premarket presiding officer procedures proceeding public disclosure Regulations and Policy regulatory request requirements sioner sory submission submitted Subpart tion tive tors for Science
Popular passages
Page 300 - food additive" means any substance the intended use of which results or may reasonably be expected to result, directly or indirectly, in its becoming a component or otherwise affecting the characteristics of any food...
Page 329 - 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 191 - 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 467 - Department of Agriculture (Parts 2900—2999) XXX Office of the Chief Financial Officer, Department of Agriculture (Parts 3000—3099) XXXI Office of Environmental Quality, Department of Agriculture (Parts 3100—3199) XXXII Office of Procurement and Property Management, Department of Agriculture (Parts 3200—3299) Chap.
Page 210 - ... would disclose techniques and procedures for law enforcement investigations or prosecutions, or would disclose guidelines for law enforcement investigations or prosecutions if such disclosure could reasonably be expected to risk circumvention of the law...
Page 412 - 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 240 - ... 9 ) to either House of Congress, or, to the extent of matter within its jurisdiction, any committee or subcommittee thereof, any joint committee of Congress or subcommittee of any such joint committee...
Page 195 - Never use any information coming to him confidentially in the performance of governmental duties as a means for making private profit. 9. Expose corruption wherever discovered. 10. Uphold these principles, ever conscious that public office is a public trust.
Page 304 - Except when an expedited review procedure is used (see §56.110), review proposed research at convened meetings at which a majority of the members of the IRB are present, including at least one member whose primary concerns are in nonscientific areas. In order for the research to be approved, it shall receive the approval of a majority of those members present at the meeting.
Page 5 - Labeling includes all written, printed, or graphic matter accompanying an article at any time while such article is in interstate commerce or held for sale after shipment or delivery in interstate commerce. (b) "Label" means any display of written, printed, or graphic matter on the immediate container of any article, or any such matter affixed to any consumer commodity or affixed to or appearing upon a package containing any consumer commodity.