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 84
... prepared in a way that does not re- veal confidential information . ( e ) Quantitative or semiquantitative formulas . Information on product design or construction . ( ii ) Material submitted under para- graph ( j ) ( 2 ) of this ...
... prepared in a way that does not re- veal confidential information . ( e ) Quantitative or semiquantitative formulas . Information on product design or construction . ( ii ) Material submitted under para- graph ( j ) ( 2 ) of this ...
Side 99
... prepared by an FDA representa- tive in all cases . ( c ) A meeting with a person outside the Department , including a person in the executive or legislative branch of the Federal Government , concerning a pending court case ...
... prepared by an FDA representa- tive in all cases . ( c ) A meeting with a person outside the Department , including a person in the executive or legislative branch of the Federal Government , concerning a pending court case ...
Side 100
... prepared by an FDA representative . ( g ) A person who participates in a meeting described in paragraphs ( b ) through ( f ) of this section may also prepare and submit to FDA for inclu- sion in the administrative file a writ- ten ...
... prepared by an FDA representative . ( g ) A person who participates in a meeting described in paragraphs ( b ) through ( f ) of this section may also prepare and submit to FDA for inclu- sion in the administrative file a writ- ten ...
Side 102
... preparation of a draft of the final notice or regulation , a representative of FDA may discuss the proposal with an ... prepared solely on the basis of the administrative record . ( ii ) If additional technical informa- tion from a ...
... preparation of a draft of the final notice or regulation , a representative of FDA may discuss the proposal with an ... prepared solely on the basis of the administrative record . ( ii ) If additional technical informa- tion from a ...
Side 108
... prepared and made publicly avail- able each week showing , to the extent feasible , for the following 4 weeks , the public meetings , conferences , hearings , advisory committee meetings , semi- nars , and other public proceedings of ...
... prepared and made publicly avail- able each week showing , to the extent feasible , for the following 4 weeks , the public meetings , conferences , hearings , advisory committee meetings , semi- nars , and other public proceedings of ...
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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 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 restrictions 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...