The Code of Federal Regulations of the United States of AmericaU.S. Government Printing Office, 1991 - 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 8
... conform- ance with the labeling requirements of this part . Similarly , when such confec- tionery items are sold in bags or boxes , such items shall be exempt from the labeling requirements of this part , in- cluding the required ...
... conform- ance with the labeling requirements of this part . Similarly , when such confec- tionery items are sold in bags or boxes , such items shall be exempt from the labeling requirements of this part , in- cluding the required ...
Page 10
... conform- ance with the labeling requirements of this part . ( ii ) Twelve shell eggs packaged in a carton designed to hold 1 dozen eggs are exempt from the placement re- quirements for the declaration of con- tents prescribed by ...
... conform- ance with the labeling requirements of this part . ( ii ) Twelve shell eggs packaged in a carton designed to hold 1 dozen eggs are exempt from the placement re- quirements for the declaration of con- tents prescribed by ...
Page 11
... conform- ance with all labeling requirements of this part ; or ( 2 ) When such cosmetics are sold at retail as part of a cosmetic package consisting of an inner and outer con- tainer and the inner container is not for separate retail ...
... conform- ance with all labeling requirements of this part ; or ( 2 ) When such cosmetics are sold at retail as part of a cosmetic package consisting of an inner and outer con- tainer and the inner container is not for separate retail ...
Page 21
... conforming to § 314.55 of this chapter is acceptable in lieu of a full new drug application for any product included in the classes of products in paragraph ( e ) of this section . A finding has been made that an ANDA may be submitted ...
... conforming to § 314.55 of this chapter is acceptable in lieu of a full new drug application for any product included in the classes of products in paragraph ( e ) of this section . A finding has been made that an ANDA may be submitted ...
Page 214
... conform to the EIS format ( 40 CFR 1502.10 ) unless there is a compelling reason to do otherwise . Subpart D - Agency Decisionmaking § 25.40 Procedures for incorporating envi- ronmental considerations into agency decisionmaking . ( a ) ...
... conform to the EIS format ( 40 CFR 1502.10 ) unless there is a compelling reason to do otherwise . Subpart D - Agency Decisionmaking § 25.40 Procedures for incorporating envi- ronmental considerations into agency decisionmaking . ( a ) ...
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Common terms and phrases
acid action additive shall conform administrative record advisory committee agency amended amounts consistent animal drug approval batches thereof cations CDER Center certifica chapter color additive D&C Color additive mixtures coloring foods coloring purposes Compliance conform in identity contain Cosmetic Act D&C Orange D&C Red D&C Yellow Department Deputy Direc diluents Director and Deputy Dockets Management Branch Drug Administration drug application employee environmental Exemption from certification externally applied drugs FD&C Federal Food FEDERAL REGISTER filed food additive Food and Drug hearing Identity and specifications issue Lead as Pb listed manufacturing practice matter ment metic million mixtures for coloring mixtures prepared therefrom notice Packaging and Labeling paragraph participant person petition presiding officer procedures public disclosure public health regulations regulatory request requirements of section restrictions revised safely Service sodium salts standards of identity submitted Subpart thereof are exempt tive Total color
Popular passages
Page 227 - Minimal risk means that the probability and magnitude of harm or discomfort anticipated in the research are not greater in and of themselves than those ordinarily encountered In daily life or during the performance of routine physical or psychological examinations or tests.
Page 158 - For the purposes of sections 205 and 207 of this title, the term "official responsibility" means the direct administrative or operating authority, whether intermediate or final, and either exercisable alone or with others, and either personally or through subordinates, to approve, disapprove, or otherwise direct Government action.
Page 168 - A trade secret may consist of any formula, pattern, device or compilation of information which is used in one's business, and which gives him an opportunity to obtain an advantage over competitors who do not know or use it.
Page 218 - 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 195 - Congress or subcommittee of any such joint committee; (10) To the Comptroller General, or any of his...
Page 230 - IRB's use of the expedited review procedure. §46.111 Criteria for IRB approval of research. a. In order to approve research covered by this policy, the IRB shall determine that all of the following requirements are satisfied: 1. Risks to subjects are minimized: (i) by using procedures which are consistent with sound research design and which do not unnecessarily expose subjects to risk, and (ii) whenever appropriate, by using procedures already being performed on the subjects for diagnostic or treatment...
Page 195 - ... (5) to a recipient who has provided the agency with advance adequate written assurance that the record will be used solely as a statistical research or reporting record, and the record is to be transferred in a form that is not individually identifiable ; (6) to the National Archives...
Page 229 - ... review more often than annually and which projects need verification from sources other than the investigators that no material changes have occurred since previous IRB review...
Page 56 - A guaranty or undertaking referred to in section 5(b)(2) of the act may be: (1) Limited to a specific shipment or other delivery of an article, in which case it may be a part of or attached to the invoice or bill of sale covering such shipment or delivery; or (2...
Page 222 - An explanation of whom to contact for answers to pertinent questions about the research and research subjects' rights, and whom to contact in the event of a research-related injury to the subject. (8) A statement that participation is voluntary...