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, 1988 - 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 5
... Application for authorization to rela- bel and recondition . 1.96 Granting of authorization to relabel and recondition . 1.97 Bonds . 1.99 Costs chargeable in connection with relabeling and reconditioning inadmissi- ble imports ...
... Application for authorization to rela- bel and recondition . 1.96 Granting of authorization to relabel and recondition . 1.97 Bonds . 1.99 Costs chargeable in connection with relabeling and reconditioning inadmissi- ble imports ...
Page 14
... application . If such application is not submitted at or prior to the hearing , the district director shall specify a time limit , reasonable in the light of the circumstances , for filing such application . § 1.95 Application for ...
... application . If such application is not submitted at or prior to the hearing , the district director shall specify a time limit , reasonable in the light of the circumstances , for filing such application . § 1.95 Application for ...
Page 15
... application for relief there- from , upon the payment of a lesser amount or upon such other terms and conditions as shall be deemed appro- priate under the law and in view of the circumstances , but the collector shall not act under ...
... application for relief there- from , upon the payment of a lesser amount or upon such other terms and conditions as shall be deemed appro- priate under the law and in view of the circumstances , but the collector shall not act under ...
Page 20
... application , a new animal drug application , or in the case of a certifiable antibiotic an Antibiotic Form 5 or 6 for the drug product has been approved , a petition has been filed as provided by paragraph ( f ) of this section , and ...
... application , a new animal drug application , or in the case of a certifiable antibiotic an Antibiotic Form 5 or 6 for the drug product has been approved , a petition has been filed as provided by paragraph ( f ) of this section , and ...
Page 21
... application or a new animal drug application for the drug product containing chlorofluorocarbon be withdrawn and that the right to a hearing on the withdrawal of the ap- plication is waived . ( h ) ( 1 ) Each manufacturer of a drug ...
... application or a new animal drug application for the drug product containing chlorofluorocarbon be withdrawn and that the right to a hearing on the withdrawal of the ap- plication is waived . ( h ) ( 1 ) Each manufacturer of a drug ...
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Common terms and phrases
74 Stat acid Act Record System advisory committee agency amounts consistent animal drug annatto approval authorized batches thereof Biologics Canthaxanthin cations certifica chapter color additive D&C color additive mixtures coloring foods coloring purposes Compliance conform in identity contain Cosmetic Act D&C Red Data and information Deputy Direc diluents Director and Deputy Dockets Management Branch Drug Administration drug application Drug Products Effective date confirmed employee environmental Exemption from certification FD&C Federal Food FEDERAL REGISTER filed food additive Food and Drug hearing human Identity and specifications institutional review board issue Lead as Pb listed manufacturing practice matter medical devices ment metic million mixtures for coloring mixtures prepared therefrom notice paragraph participation percent person petition presiding officer Privacy Act Record procedures public disclosure public health recall regulations regulatory request restrictions revised standards of identity submitted thereof are exempt tive
Popular passages
Page 165 - 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 154 - Government, either directly or indirectly, which is inconsistent with the conscientious performance of his governmental duties. 8. 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 327 - 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 64 - advisory committee" means any committee, board, commission, council, conference, panel, task force, or other similar group, or any subcommittee or other subgroup thereof...
Page 190 - September 27, 1975. (h) Rights of Legal Guardians. For the purposes of this section, the parent of any minor, or the legal guardian of any individual who has been declared to be incompetent due to physical or mental incapacity or age by a court of competent jurisdiction, may act on behalf of the individual.
Page 254 - The petition shall be submitted in triplicate. If any part of the material submitted is in a foreign language, it shall be accompanied by an accurate and complete English translation. The...
Page 188 - ... (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 221 - ... 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 221 - ... and welfare of human subjects. In addition to possessing the professional competence necessary to review specific research activities, the IRB shall be able to ascertain the acceptability of proposed research in terms of institutional commitments and regulations, applicable law, and standards of professional conduct and practice. The IRB shall therefore include persons knowledgeable in these areas. If an IRB regularly reviews research that involves a vulnerable category of subjects, such as children,...