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 |
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Page 12
... described in this section to the individual or the organization to whom the information pertains or to an authorized represent- ative of either will not be deemed a dis- closure within the meaning of this part . $ 5.72 Records available ...
... described in this section to the individual or the organization to whom the information pertains or to an authorized represent- ative of either will not be deemed a dis- closure within the meaning of this part . $ 5.72 Records available ...
Page 13
... described in §5.73 if he de- termines that disclosure is in the pub- lic interest and is consistent with obli- gations of confidentiality and adminis- trative necessity . ( b ) In making such a determination , consideration may be given ...
... described in §5.73 if he de- termines that disclosure is in the pub- lic interest and is consistent with obli- gations of confidentiality and adminis- trative necessity . ( b ) In making such a determination , consideration may be given ...
Page 30
... described in 8.5 ( a ) ( 1 ) , must be made on an employee or former employee who has custody of the records , with a copy simultaneously delivered to the General Counsel at the address listed in paragraph ( b ) of this section . For as ...
... described in 8.5 ( a ) ( 1 ) , must be made on an employee or former employee who has custody of the records , with a copy simultaneously delivered to the General Counsel at the address listed in paragraph ( b ) of this section . For as ...
Page 31
... described in paragraph ( a ) ( 1 ) of this section is required before the Secretary determines whether to allow an employee to produce those records , the employee or counsel for the em- ployee shall— ( 1 ) Inform the court or other ...
... described in paragraph ( a ) ( 1 ) of this section is required before the Secretary determines whether to allow an employee to produce those records , the employee or counsel for the em- ployee shall— ( 1 ) Inform the court or other ...
Page 32
... described in §12.5 that formally applies to be a transferee or lessee of surplus Federal real property , using a public benefit allowance ( PBA ) under the Act . Lessee , except as used in §12.14 ( a ) ( 5 ) , means an entity that is ...
... described in §12.5 that formally applies to be a transferee or lessee of surplus Federal real property , using a public benefit allowance ( PBA ) under the Act . Lessee , except as used in §12.14 ( a ) ( 5 ) , means an entity that is ...
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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.