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, 2000 Special edition of the Federal Register, containing a codification of documents of general applicability and future effect ... with ancillaries. |
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Side 41
... manufacturing practice for positron emission tomography radio- pharmaceutical drug products . [ 47 FR 38480 , Aug. 31 , 1982 ] EDITORIAL NOTE : For FEDERAL REGISTER ci- tations affecting §5.31 , see the List of CFR Sections Affected in ...
... manufacturing practice for positron emission tomography radio- pharmaceutical drug products . [ 47 FR 38480 , Aug. 31 , 1982 ] EDITORIAL NOTE : For FEDERAL REGISTER ci- tations affecting §5.31 , see the List of CFR Sections Affected in ...
Side 45
... manufacturing practices and false or misleading labeling of new drugs , new animal drugs , and feeds bearing or containing new animal drugs . ( a ) The following officials are author- ized to perform all the functions of the ...
... manufacturing practices and false or misleading labeling of new drugs , new animal drugs , and feeds bearing or containing new animal drugs . ( a ) The following officials are author- ized to perform all the functions of the ...
Side 62
... Manufacturers of sunlamp prod- ucts and ultraviolet lamps intended for use in any sunlamp product , as defined in § 1040.20 ( b ) of this chapter . ( b ) The Director and Deputy Direc- tor , Office of Compliance , CDRH , and the ...
... Manufacturers of sunlamp prod- ucts and ultraviolet lamps intended for use in any sunlamp product , as defined in § 1040.20 ( b ) of this chapter . ( b ) The Director and Deputy Direc- tor , Office of Compliance , CDRH , and the ...
Side 65
... Manufacturing and Product Qual- ity . Office of Blood Research and Review Division of Transfusion Transmitted Dis ... Manufacturers Assistance Division of Congressional and Public Affairs . Division of Manufacturers Assistance and ...
... Manufacturing and Product Qual- ity . Office of Blood Research and Review Division of Transfusion Transmitted Dis ... Manufacturers Assistance Division of Congressional and Public Affairs . Division of Manufacturers Assistance and ...
Side 66
... Manufacturing and Product Qual- ity . Division of Scientific Investigations . Division of Prescription Drug Compliance and Surveillance . Division of Labeling and Nonprescription Drug Compliance . Office of Information Technology1 ...
... Manufacturing and Product Qual- ity . Division of Scientific Investigations . Division of Prescription Drug Compliance and Surveillance . Division of Labeling and Nonprescription Drug Compliance . Office of Information Technology1 ...
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Code of Federal Regulations: Containing a Codification of Documents of ... Uten tilgangsbegrensning - 1976 |
Code of Federal Regulations: Containing a Codification of Documents of ... Uten tilgangsbegrensning - 1976 |
Code of Federal Regulations: Containing a Codification of Documents of ... Uten tilgangsbegrensning - 1982 |
Vanlige uttrykk og setninger
acid action administrative record advisory committee agency amended amounts consistent approval Authority citation revised biological Canthaxanthin cation CDER CDRH chapter clinical color additive D&C Color additive mixtures coloring purposes Commissioner of Food Compliance conform in identity contain Cosmetic Act D&C Orange D&C Red D&C Yellow Deputy Direc Deputy Director determination diluents Director and Deputy ditive Dockets Management Branch Drug Administration drug application Effective date employee Evaluation Exemption from certification FD&C Federal Acquisition Regulation Federal Food FEDERAL REGISTER filed 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 naphthalenedisulfonic notice paragraph participation party percent person petition presiding officer procedures public disclosure quirements regulations regulatory request safely sioner sory submitted Subpart tification tion tive tors
Populære avsnitt
Side 267 - 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...
Side 441 - Advisory Council on Historic Preservation African Development Foundation Federal Acquisition Regulation Agency for International Development, United States Federal Acquisition Regulation Agricultural Marketing Service Agricultural Research Service Agriculture Department Agricultural Marketing Service Agricultural Research Service Animal and Plant Health Inspection Service Chief Financial Officer, Office of Commodity Credit Corporation Cooperative State Research, Education, and Extension Service Economic...
Side 161 - 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.
Side 179 - ... could reasonably be expected to constitute an unwarranted invasion of personal privacy, d. could reasonably be expected to disclose the identity of a confidential source, including a state, local, or foreign agency or authority or any private institution which furnished information on a confidential basis...
Side 179 - ... 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...
Side 371 - 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.
Side 164 - 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.
Side xi - 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.
Side 272 - Administration has established, and published in the FEDERAL REGISTER, a list of categories of research that may be reviewed by the IRB through an expedited review procedure. The list will be amended, as appropriate, through periodic republication in the FEDERAL REGISTER.
Side 164 - Never discriminate unfairly by the dispensing of special favors or privileges to anyone, whether for remuneration or not; and never accept, for himself or his family, favors or benefits under circumstances which...