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, 1996 - 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 19
... submit to the re- sponsible Department official a concise statement of disagreement to be asso- ciated with the disputed record and dis- closed whenever the record is disclosed . ( b ) Notation and disclosure of disputed records ...
... submit to the re- sponsible Department official a concise statement of disagreement to be asso- ciated with the disputed record and dis- closed whenever the record is disclosed . ( b ) Notation and disclosure of disputed records ...
Page 29
... submit- ting a demand for testimony or records ? 8.4 What procedures are followed in re- sponse to a demand for ... submitting a demand for testimony or records ? ( a ) A demand for testimony of an em- ployee or former employee , or a de ...
... submit- ting a demand for testimony or records ? 8.4 What procedures are followed in re- sponse to a demand for ... submitting a demand for testimony or records ? ( a ) A demand for testimony of an em- ployee or former employee , or a de ...
Page 46
... submit- ted by the attorney was computed ; and ( ii ) The actual time expended for the fee . ( 7 ) A written verification under oath , affirmation , or under penalty of per- jury that the information contained in the application and any ...
... submit- ted by the attorney was computed ; and ( ii ) The actual time expended for the fee . ( 7 ) A written verification under oath , affirmation , or under penalty of per- jury that the information contained in the application and any ...
Page 47
... submit addi- tional information . ( Authority : 5 U.S.C. 504 ( a ) ( 2 ) and ( c ) ( 1 ) ) §21.32 Confidentiality of information about net worth . ( a ) In a proceeding on an application , the public record ordinarily includes the ...
... submit addi- tional information . ( Authority : 5 U.S.C. 504 ( a ) ( 2 ) and ( c ) ( 1 ) ) §21.32 Confidentiality of information about net worth . ( a ) In a proceeding on an application , the public record ordinarily includes the ...
Page 64
... submission by the employee of knowingly false statements , rep- resentations or evidence may subject the employee to ... submit , within the deadlines in paragraph ( a ) ( 1 ) of this section , a request that meets the requirements of ...
... submission by the employee of knowingly false statements , rep- resentations or evidence may subject the employee to ... submit , within the deadlines in paragraph ( a ) ( 1 ) of this section , a request that meets the requirements of ...
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Common terms and phrases
34 CFR-Continued action Administration amended amount ance applicant approved audit Authority citation revised basis benefits Budget under control cation certification cial cipient cluding compliance comply contract control number debarment debt Department desegregation disclosure discrimination documents education program educational agency effective date pending eligible employee eral facilities Federal Acquisition Regulation Federal financial assistance fiscal funds Government gram grant grantee or subgrantee handicapped persons hearing individual Insular Area LEA's magnet school Management and Budget means ment notice Office of Management OMB number paragraph participation partment party payment Pending regulation private school procedures program or activity purposes quired received recipient records Redesignated Regulation at 57 Removed effective date request retary revised effective date Secretary reviews Stat statute submit Subpart tion Title title IX vised vocational education
Popular passages
Page 281 - ... short form. (c) An IRB may waive the requirement for the investigator to obtain a signed consent form for some or all subjects if it finds either: (1) That the only record linking the subject and the research would be the consent document and the principal risk would be potential harm resulting from a breach of confidentiality. Each subject will be asked whether the subject wants documentation linking the subject with the research, and the subject's wishes will govern; or (2) That the research...
Page 280 - 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 procedures or courses of treatment, if any, that might be advantageous to the subject; (5) A statement describing the extent, if any, to which confidentiality of records identifying the subject will be maintained; (6) For research involving more than minimal risk, an explanation as to whether any compensation and an explanation as to whether any...
Page 280 - Except as provided in paragraph (c) or (d) of this section, in seeking informed consent the following information shall be provided to each subject: (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)...
Page 280 - ... unless the investigator has obtained the legally effective Informed consent of the subject or the subject's legally authorized representative. An investigator shall seek such consent only under circumstances that provide the prospective subject or the representative sufficient opportunity to consider whether or not to participate and that minimize the possibility of coercion or undue influence. The information that is given to the subject or the representative shall be in language understandable...
Page 275 - Minimal risk means that the probability and magnitude of harm or discomfort anticipated in the research are not greater in and of themselves than those ordinarily encountered in daily life or during the performance of routine physical or psychological examinations or tests.
Page 278 - Some or all of the research appearing on the list and found by the reviewer(s) to involve no more than minimal risk, (2) Minor changes in previously approved research during the period (of one year or less) for which approval is authorized. Under an expedited review procedure, the review may be carried out by the IRB chairperson or by one or more experienced reviewers designated by the chairperson from among members of the IRB. In reviewing the research, the reviewers may exercise all of the authorities...
Page 26 - Commissioner, shall leave title to such invention in the employee, subject, however, to the reservation to the Government of a nonexclusive, irrevocable, royaltyfree license in the invention with power to grant licenses for all governmental purposes, such reservation to appear, where practicable, in any patent, domestic or foreign, which may issue on such invention.
Page 278 - 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 treatment purposes. (2) Risks to subjects are reasonable...
Page 274 - Legally authorized representative means an individual or judicial or other body authorized under applicable law to consent on behalf of a prospective subject to the subject's participation in the procedure(s) involved in the research. (d) Research means a systematic investigation, including research development, testing and evaluation, designed to develop or contribute to generalizable knowledge. Activities which meet this definition constitute research for purposes of this policy, whether or not...
Page 277 - No IRB may consist entirely of members of one profession. (c) Each IRB shall include at least one member whose primary concerns are in scientific areas and at least one member whose primary concerns are in nonscientific areas. (d) Each IRB shall include at least one member who is not otherwise affiliated with the institution and who is not part of the immediate family of a person who is affiliated with the institution.