Documents
Briefs, oral arguments, agency decisions and the Federal Register.
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Food Labeling: Health Claims; Soy Protein and Coronary Heart Disease
Federal Register · Proposed Rule · Nov 10, 1998
DATES: Written comments by January 25, 1999. … This new law amended the Federal Food, Drug, and Cosmetic Act (the act) in a number of important ways.
63 FR 62977Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · May 4, 1998
SUPPLEMENTARY INFORMATION: FDA will support the research studies covered by this notice under section 301 of the Public Health Service Act (42 U.S.C. 241). … All comments received on the funding priority will be taken into consideration and will receive a response.
63 FR 24553Health and Human Services DepartmentFood and Drug AdministrationFood Additives Permitted for Direct Addition to Food for Human Consumption; Vitamin D3
Federal Register · Rule · Feb 27, 2003
Paperwork Reduction Act of 1995 VI. References VII. Objections I. … Paperwork Reduction Act of 1995 This final rule contains no collection of information.
68 FR 9000Health and Human Services DepartmentFood and Drug AdministrationPrivacy Act of 1974; System of Records
Federal Register · Notice · Dec 26, 2024
Submit any comments by January 27, 2025. ADDRESSES: The public should submit written comments, by mail or email, to Beth Kramer, HHS Privacy Act Officer, at 200 Independence Ave. … previously stated that retention varies from 1 year to permanent depending on the type of record, now cites the applicable NARA-approved disposition schedules and itemizes the record types and disposition periods
89 FR 105054Health and Human Services DepartmentFood and Drug AdministrationComprehensive List of Guidance Documents at the Food and Drug Administration
Federal Register · Notice · Aug 9, 2010
DATES: We welcome general comments on this list and on agency guidance documents at any time. ADDRESSES: Submit electronic comments to http://www.regulations.gov . … In accordance with the agency's general policy on guidances, you may comment on this list and on any FDA guidance document at any time.
75 FR 48180Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Rule · Nov 25, 2009
FDA therefore, for good cause shown, has determined that notice and public comment are unnecessary under 5 U.S.C. 553(b)(3)(B). II. … We did not intend to require that the statement remain on the label for any longer than the 1-year period from the time of introduction into interstate commerce.
74 FR 61512Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Rule · Mar 4, 2002
Publication of this document constitutes final action on these changes under the Administrative Procedure Act (5 U.S.C. 553). … In § 312.41 Comment and advice on an IND , remove the parenthetical phrase at the end of the section. § 312.44 [Amended] 39.
67 FR 9584Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Rule · Sep 27, 1996
The September 7, 1995, proposed rule also provided an opportunity for interested persons to submit comments on the proposed rule and the agency's proposed findings. … The comment period closed on January 5, 1996.
61 FR 50704Health and Human Services DepartmentFood and Drug AdministrationFood Safety Research: Availability of Cooperative Agreements; Request for Applications
Federal Register · Notice · May 27, 1998
SUPPLEMENTARY INFORMATION: FDA will support the research studies covered by this notice under section 301 of the Public Health Service Act (the PHS Act) (42 U.S.C. 241). … A final FSR (SF-269), Program Progress Report and Invention Statement, must be submitted within 90 days after the expiration of the project period, as noted on the Notice of Grant Award.
63 FR 29016Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Rule · Mar 19, 2021
A notice published pursuant to section 512(i) is not subject to the notice-and-comment rulemaking requirements of the Administrative Procedure Act, 5 U.S.C. 551 et seq. … For No. 069254: Zero withdrawal period.
86 FR 14815Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Aug 7, 1997
On September 26, 1994, Duramed submitted ANDA 40-115 for Cenestin (conjugated estrogens tablets) under section 505 (j) of the Federal Food, Drug, and Cosmetic Act (the act) (21 U.S.C. 355(j)). … Any other interested person may also submit comments on this notice.
62 FR 42562Health and Human Services DepartmentFood and Drug AdministrationFood Labeling: Front-of-Package Nutrition Information
Federal Register · Proposed Rule · Jan 16, 2025
Submit comments (including recommendations) on the collection of information under the Paperwork Reduction Act of 1995 by May 16, 2025. ADDRESSES: You may submit comments as follows. … Under the Paperwork Reduction Act (PRA), comments on the information collection provisions are best assured of consideration if your comments are received by May 16, 2025.
90 FR 5426Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Feb 19, 2010
Reduction Act. 4. … Determines compliance of petitions, comments, request for hearings, motions, briefs, and objections with Agency regulations. 4.
75 FR 7490Health and Human Services DepartmentFood and Drug AdministrationFood Additive Regulations; Incorporation by Reference of the Food Chemicals Codex, 7th Edition
Federal Register · Rule · Nov 29, 2013
Follow the instructions for submitting comments. … Section 301(ll) of the Federal Food, Drug, and Cosmetic Act Our review of this petition was limited to section 409 of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. 348).
78 FR 71457Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Aug 18, 2009
and the Paperwork Reduction Act. … Determines compliance of petitions, comments, request for hearings, motions, briefs, and objections with agency regulations. 4.
74 FR 41713Health and Human Services DepartmentFood and Drug AdministrationDelegations of Authority and Organization; Reorganization and Republication
Federal Register · Rule · Jun 8, 2001
the issuance of notices of filing (including notices of extension of, or reopening of, the comment period), and of voluntary withdrawal, of petitions on food additives, generally recognized as safe (GRAS … the issuance of proposed rulemaking (including notices of extension of, or reopening of, the comment period) pertaining to food standards.
66 FR 30992Health and Human Services DepartmentFood and Drug Administration
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