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Federal Register · Notice · Sep 14, 2005
Under the Paperwork Reduction Act of 1995 (the PRA), Federal agencies are required to publish a notice in the Federal Register concerning each proposed collection of information and to allow 60 days … for public comment in response to the notice.
70 FR 54390Health and Human Services DepartmentFood and Drug AdministrationImplementation of Sanitary Food Transportation Act of 2005
Federal Register · Proposed Rule · Apr 30, 2010
A Class I recall was issued for the dog food and other food for animals manufactured at the same plant within the same time period. … What industry standards exist for the cleaning of food transportation vehicles? Question 2b.
75 FR 22713Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Aug 8, 2003
(the act) (21 U.S.C. 360b). … Any other interested person may also submit comments on this document.
68 FR 47332Health and Human Services DepartmentFood and Drug AdministrationNational Environmental Policy Act; Proposed Revision of Policies and Procedures
Federal Register · Proposed Rule · Apr 3, 1996
(the act) or the Public Health Service Act (the PHS Act). … As a result of this review, FDA has found that FDA-regulated articles produced in compliance with all applicable emission requirements (e.g., Clean Air Act, Clean Water Act, Occupational Safety and Health
61 FR 14922Health and Human Services DepartmentFood and Drug AdministrationNational Environmental Policy Act; Proposed Revision of Policies and Procedures
Federal Register · Proposed Rule · May 1, 1996
(the act) or the Public Health Service Act (the PHS Act). … As a result of this review, FDA has found that FDA-regulated articles produced in compliance with all applicable emission requirements (e.g., Clean Air Act, Clean Water Act, Occupational Safety and Health
61 FR 19476Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Nov 7, 2002
(the act) (21 U.S.C. 360c(f)(2)). … the act.
67 FR 67859Health and Human Services DepartmentFood and Drug AdministrationSubstances Prohibited From Use in Animal Food or Feed
Federal Register · Proposed Rule · Oct 6, 2005
FDA has been concerned about the adequacy of such clean-out procedures and sought public comment on this issue in the 2002 ANPRM. … (the act)
70 FR 58570Health and Human Services DepartmentFood and Drug AdministrationProduct-Specific Guidances; Draft and Revised Draft Guidances for Industry; Availability
Federal Register · Notice · Aug 23, 2024
Under that process, draft guidances are posted on FDA's website and announced periodically in the Federal Register . … Paperwork Reduction Act of 1995 While these guidances contain no collection of information, they do refer to previously approved FDA collections of information.
89 FR 68162Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Rule · Apr 12, 2019
Section 513(f)(6)(D)(i) also requires that FDA publish a final action classifying suitable accessories into class I within 180 days after the end of the comment period. … An air-handling apparatus accessory is a supplementary device that is intended to be used with an air-handling apparatus for a surgical operating room.
84 FR 14865Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Proposed Rule · Feb 19, 2003
The comment further stated that potable eyewash units should be flushed and cleaned and the water and concentrate replaced every 60 days. … Comment No. AP. 2. Comment 1. 3. Comment 2. 4. Comment 3. 5. Comment 4. 6. Comment 5. 7. Comment 6. 8.
68 FR 7951Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Jul 31, 2013
control environmental conditions and inspection result records; (4) requirements for personnel hygiene; (5) procedures for preventing contamination of equipment and products; (6) equipment adjustment, cleaning … 25,986 6 155,916 Distribution procedures and records—820.160(a) and (b) 25,986 1 25,986 1 25,986 Installation—820.170 25,986 1 25,986 2 51,972 Record retention period
78 FR 46347Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Mar 1, 2024
Background Section 204 of the Food and Drug Administration Modernization Act of 1997 (Pub. L. 105-115) amended section 514 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 360d). … Such standards are those that FDA has recognized by notice published in the Federal Register or that FDA has decided to recognize but for which recognition is pending (because a periodic notice has
89 FR 15202Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Dec 5, 2016
ADDRESSES: To ensure that comments on the information collection are received, OMB recommends that written comments be faxed to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk … Medical Device: Current Good Manufacturing Practice Quality System Regulations— OMB Control Number 0910-0073—Extension Under section 520(f) of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (
81 FR 87572Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Nov 15, 2019
ADDRESSES: To ensure that comments on the information collection are received, OMB recommends that written comments be faxed to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk … In the Federal Register of July 31, 2019 (84 FR 37317), FDA published a 60-day notice requesting public comment on the proposed collection of information. No comments were received.
84 FR 62534Health and Human Services DepartmentFood and Drug AdministrationFood Labeling; Gluten-Free Labeling of Fermented or Hydrolyzed Foods
Federal Register · Proposed Rule · Nov 18, 2015
For example, manufacturers may use physical barriers (such as walls, curtains, or distance) or air handling as a means of isolating the production line and by cleaning and sanitizing equipment between … Such a time period is consistent with other FDA regulations, but we invite comment on whether we should use a different recordkeeping period.
80 FR 71990Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Apr 4, 2016
Background Section 204 of the Food and Drug Administration Modernization Act of 1997 (FDAMA) (Pub. … L. 105-115) amended section 514 of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. 360d).
81 FR 19196Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Proposed Rule · Nov 24, 1998
DATES: Submit written comments by February 8, 1999. Written comments on the information collection requirements should be submitted by December 24, 1998. … Request for Comments Interested persons may on or before February 8, 1999, submit to the Dockets Management Branch (address above) written comments regarding this notice.
63 FR 64930Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Sep 24, 1998
The comments in the docket will be periodically reviewed, and, where appropriate, the guidance will be amended. … These would include diet, cleaning and feeding schedules, provisions for periodic veterinary care if applicable, and details of special handling that the animals may require once inoculated.
63 FR 51074Health and Human Services DepartmentFood and Drug AdministrationDraft Multi-Agency Radiological Laboratory Analytical Protocols Manual
Federal Register · Notice · Aug 31, 2001
Kruger, Acting Director, Office of Radiation and Indoor Air. For the Environmental Protection Agency, dated this 28th day of July, 2001. Larry G. … Reed, Acting Director, Office of Emergency and Remedial Response. For the Food and Drug Administration, dated this 26th day of July, 2001. Michael C.
66 FR 45972Defense DepartmentEnergy DepartmentAnimal Drugs, Feeds, and Related Products; Chlortetracycline
Federal Register · Rule · Jul 9, 1996
The authority citation for 21 CFR part 558 continues to read as follows: Authority: Secs. 512, 701 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360b, 371). 4. … Beaulieau, Acting Director, Office of New Animal Drug Evaluation, Center for Veterinary Medicine. [FR Doc. 96-17169 Filed 7-8-96; 8:45 am] BILLING CODE 4160-01-F
61 FR 35949Health and Human Services DepartmentFood and Drug Administration
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