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 26
... ) Administrative staff manuals and instructions to staff that affect the public . ( We will not make available , however , manuals or instructions that reveal investigative or audit 26 § 5.51 45 CFR Subtitle A ( 10-1-91 Edition )
... ) Administrative staff manuals and instructions to staff that affect the public . ( We will not make available , however , manuals or instructions that reveal investigative or audit 26 § 5.51 45 CFR Subtitle A ( 10-1-91 Edition )
Page 27
however , manuals or instructions that reveal investigative or audit proce- dures as described in §§ 5.63 and 5.68 of this part . ) ( b ) Other records . In addition to such records as those described in paragraph ( a ) of this section ...
however , manuals or instructions that reveal investigative or audit proce- dures as described in §§ 5.63 and 5.68 of this part . ) ( b ) Other records . In addition to such records as those described in paragraph ( a ) of this section ...
Page 44
... audits or utilization review . ( 103 ) Disclosures in the course of employ- ee discipline or competence determination proceedings . APPENDIX C to Part 5b - DELEGATIONS OF AUTHORITY [ RESERVED ] PART 6 - INVENTIONS AND PATENTS ( GENERAL ) ...
... audits or utilization review . ( 103 ) Disclosures in the course of employ- ee discipline or competence determination proceedings . APPENDIX C to Part 5b - DELEGATIONS OF AUTHORITY [ RESERVED ] PART 6 - INVENTIONS AND PATENTS ( GENERAL ) ...
Page 86
... audit finding of inad- equate documentation might involve thousands of receipts ) , the Board will consult with the parties about how to reduce the size of the file . § 16.9 How the Board will promote devel- opment of the record . The ...
... audit finding of inad- equate documentation might involve thousands of receipts ) , the Board will consult with the parties about how to reduce the size of the file . § 16.9 How the Board will promote devel- opment of the record . The ...
Page 89
... audit disallowance would be on the grantee's contractor , not on the grant- ee ) , the Board may allow the third person to present the case on appeal for the appellant or to appear with a party in the case , after consultation with the ...
... audit disallowance would be on the grantee's contractor , not on the grant- ee ) , the Board may allow the third person to present the case on appeal for the appellant or to appear with a party in the case , after consultation with the ...
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action Administration agreement amended amicus curiae amount ance applicable appropriate approval audit authority award benefits Block Grant Board cation child care services cial cluding compliance comply contract debarment debt decision Department determined discrimination documents eligible employee employment entity equipment eral facilities Federal agency Federal financial assistance FEDERAL REGISTER Government gram grantee or subgrantee handicapped persons Health and Human Health Service hearing Human Services ICRC individual institution insular area issued means ment national origin notice notify operation organization paragraph participation partment party payment period presiding officer procedures program or activity prohibited proposed Public Health purpose pursuant quired real property received recipient records regulations request responsible section 504 Single Audit sion Social Security Act specific Stat statute submit Subpart tion Title title IX unless vocational education
Popular passages
Page 325 - Subject an individual to segregation or separate treatment in any matter related to his receipt of any service, financial aid, or other benefit under the program...
Page 124 - IRB's use of the expedited review procedure. §690.111 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...
Page 46 - The Government shall obtain the entire domestic right, title and interest in and to all inventions made by any Government employee (i) during working hours, or (ii) with a contribution by the Government of facilities, equipment, materials, funds, or information, or of time or services of other Government employees on official duty, or (iii) which bear a direct relation to or are made in consequence of the official duties of the inventor.
Page 126 - An IRB may approve a consent procedure which does not include, or which alters, some or all of the elements of informed consent set forth above...
Page 337 - ... other entity, or any individual, in any State, to whom Federal financial assistance is extended, directly or through another recipient, for any program, including any successor, assign, or transferee thereof, but such term does not include any ultimate beneficiary under any such program. (i) The term "primary recipient...
Page 120 - Human subject means a living individual about whom an investigator (whether professional or student) conducting research obtains (1) Data through intervention or interaction with the individual, or (2) Identifiable private information.
Page 258 - Secretary or his delegate, under any of the following methods: (1) the straight line method, (2) the declining balance method, using a rate not exceeding twice the rate which would have been used had the annual allowance been computed under the method described in paragraph (1).
Page 125 - ... (1) A statement that the study involves research, an explanation of the purposes of the research and the expected duration of the subject's participation, a description of the procedures to be followed, and identification of any procedures which are experimental; (2) A description of any reasonably foreseeable risks or discomforts to the subject; (3) A description of any benefits to the subject or to others which may reasonably be expected from the research; (4) A disclosure of appropriate alternative...
Page 124 - Risks to subjects are reasonable in relation to anticipated benefits, if any, to subjects, and the importance of the knowledge that may reasonably be expected to result. In evaluating risks and benefits, the IRB should consider only those risks and benefits that may result from the research (as distinguished from risks and benefits of therapies subjects would receive even if not participating in the research). The IRB should not consider possible long-range effects of applying knowledge gained in...
Page 67 - An individual or family that has a primary nighttime residence that is: (i) A supervised publicly or privately operated shelter designed to provide temporary living accommodations (including welfare hotels, congregate shelters, and transitional housing for the mentally ill); (ii) An institution that provides a temporary residence for individuals intended to be institutionalized; or (ill) A public or private place not designed for, or ordinarily used as, a regular sleeping accommodation for human...