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National Toxicology Program; Announcement of Intent To Conduct Toxicological Studies of 22 Chemicals
Federal Register · Uncategorized Document · Sep 12, 1994
DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service National Toxicology Program; Announcement of Intent To Conduct Toxicological Studies of 22 Chemicals Request for Comments: As part of … Cresols are on the list of Hazardous Air Pollutants in the Clean Air Act Amendments of 1990 and on the Superfund Priority List of Hazardous Substances.
Health and Human Services DepartmentPublic Health ServiceProposed Data Collections Submitted for Public Comment and Recommendations
Federal Register · Notice · Jul 18, 2003
In 1982, periodic sampling of drinking water sources began at Camp Lejeune to comply with regulations of the national Safe Drinking Water Act. … These chemicals are used as solvents to clean machinery and weapons and in dry cleaning operations.
68 FR 42732Health and Human Services DepartmentCenters for Disease Control and PreventionFederal Register · Rule · Sep 19, 1996
clean'' claims for which payment is not issued within 30 calendar days. … An advance payment is a ``payment'' under section 1842(c)(2)(C) of the Act for purposes of meeting the time limit for the payment of clean claims, to the extent of the advance payment.
61 FR 49271Health and Human Services DepartmentFederal Register · Notice · Sep 24, 2008
Current Good Manufacturing Practice Regulations for Finished Pharmaceuticals (OMB Control Number 0910-0139)—Extension Under section 501(a)(2)(B) of the Federal Food, Drug, and Cosmetic Act (the act) ( … FDA has the authority under section 701(a) of the act (21 U.S.C. 371(a)) to issue regulations for the efficient enforcement of the act regarding CGMP procedures for manufacturing, processing, and holding
73 FR 55108Health and Human Services DepartmentFood and Drug AdministrationMedicare and Medicaid Programs; Fire Safety Requirements for Certain Health Care Facilities
Federal Register · Rule · May 4, 2016
(the Act). … Many of the public comments received during the comment period strongly encouraged CMS to adopt the 2012 edition of the LSC.
81 FR 26872Health and Human Services DepartmentCenters for Medicare & Medicaid ServicesFederal Register · Notice · Sep 28, 2011
The FDA has the authority under Section 701(a) of the FD&C Act (21 U.S.C. 371(a)) to issue regulations for the efficient enforcement of the FD&C Act regarding CGMP procedures for manufacturing, processing … Thereafter, SOPs need to be periodically updated. A combined estimate for routine maintenance of SOPs is provided in table 1 of this document.
76 FR 60052Health and Human Services DepartmentFood and Drug AdministrationProposed Data Collections Submitted for Public Comment and Recommendations
Federal Register · Notice · May 4, 2004
In 1982, periodic sampling of drinking water sources began at Camp Lejeune to comply with regulations of the national Safe Drinking Water Act. … These chemicals are used as solvents to clean machinery and weapons and in dry cleaning operations.
69 FR 24602Health and Human Services DepartmentCenters for Disease Control and PreventionFederal Register · Notice · Apr 28, 2008
CGMP Regulations for Finished Pharmaceuticals—21 CFR Parts 210 and 211 (OMB Control Number 0910-0139)—Extension Under section 501(a)(2)(B) of the Federal Food, Drug, and Cosmetic Act (the act) (21 U.S.C … FDA has the authority under section 701(a) of the act (21 U.S.C. 371(a)) to issue regulations for the efficient enforcement of the act regarding CGMP procedures for manufacturing, processing, and holding
73 FR 22951Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Feb 7, 2002
CGMP Regulations for Finished Pharmaceuticals—21 CFR Parts 210 and 211 (OMB Control No. 0910-0139)—Extension Under section 501(a)(2)(B) of the Federal Food, Drug, and Cosmetic Act (the act) (21 U.S.C. … Section 211.56(c)—Use of suitable rodenticides, insecticides, fungicides, fumigating agents, and cleaning and sanitizing agents; 4. Section 211.67(b)—Cleaning and maintenance of equipment; 5.
67 FR 5825Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Jul 25, 2005
• Section 211.182—Specifies requirements for equipment cleaning records and the use log. … Thereafter, SOPs need to be periodically updated. A combined estimate is provided in table 1 of this document.
70 FR 42579Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · May 31, 2011
FDA has the authority under section 701(a) of the FD&C Act (21 U.S.C. 371(a)) to issue regulations for the efficient enforcement of the FD&C Act regarding CGMP procedures for manufacturing, processing, … Thereafter, SOPs need to be periodically updated. A combined estimate for routine maintenance of SOPs is provided in table 1 of this document.
76 FR 31342Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Aug 20, 1999
DATES: Written comments must be received on or before October 19, 1999. ADDRESSES: Address all comments concerning this notice to Joseph G. … Actions taken to comply with requirements of applicable legislation or regulations (e.g., meet emissions requirements established pursuant to Clean Air Act). 17.
64 FR 45558Health and Human Services DepartmentNational Institutes of HealthFederal Register · Proposed Rule · Apr 10, 1998
Section 4 of Executive Order 12889 states that any agency subject to the Administrative Procedure Act shall provide a 75-day comment period for any proposed technical regulation. … As a result, a 75-day comment period is not required for this proposed rule. VII. References 1.
63 FR 17744Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · May 30, 2001
Chornobyl Accident SUMMARY: In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for opportunity for public comment on proposed data collection projects … Cases and controls (or proxies) will be interviewed to provide details of their work during the Chornobyl clean-up operation.
66 FR 29336Health and Human Services DepartmentNational Institutes of HealthFederal Register · Notice · Jun 11, 2012
Under these acts, a product's regulatory review period forms the basis for determining the amount of extension an applicant may receive. … FDA has determined that the applicable regulatory review period for Progel Pleural Air Leak Sealant is 3,854 days.
77 FR 34389Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Jun 6, 1997
However, as permitted by section 520(l)(5)(C) of the act, in the Federal Register of November 30, 1992 (57 FR 56586), the agency published a notice extending the period for issuing such regulations until … aids and accessory cleaning pads).
62 FR 31118Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Mar 28, 2005
CGMP Regulations for Finished Pharmaceuticals—21 CFR Parts 210 and 211 (OMB Control Number 0910-0139)—Extension Under section 501(a)(2)(B) of the Federal Food, Drug, and Cosmetic Act (the act) (21 … • Section 211.182—Specifies requirements for equipment cleaning records and the use log.
70 FR 15628Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Jul 17, 2019
Under section 701(a) of the FD&C Act (21 U.S.C. 371(a)), FDA is authorized to issue regulations for the efficient enforcement of the FD&C Act. … Records are maintained on file at each farm site and examined there periodically by FDA inspectors.
84 FR 34191Health and Human Services DepartmentFood and Drug AdministrationMedical Devices; Reprocessed Single-Use Devices; Requirement for Submission of Validation Data
Federal Register · Rule · Sep 25, 2006
days after the comment period on this direct final rule ends. … The comment period for this direct final rule runs concurrently with the comment period of the companion proposed rule.
71 FR 55729Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · May 16, 2002
DATES: Submit written comments on the collection of information by June 17, 2002. … In the Federal Register of February 7, 2002 (67 FR 5825), the agency requested comments on the proposed collection of information. There were no comments received.
67 FR 34939Health and Human Services DepartmentFood and Drug Administration
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