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, 1991 Special edition of the Federal Register, containing a codification of documents of general applicability and future effect ... with ancillaries. |
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action Administration agreement amended amicus curiae amount ance appeal applicable appropriate approval audit authority award benefits Block Grant Board cation child cial claim cluding compliance comply conduct contract debarment debt debtor decision Department determined disclosure discrimination documents eligible employee employment entity equipment eral facilities Federal Acquisition Regulation Federal agency Federal financial assistance FEDERAL REGISTER Government gram grant or subgrant grantee handicapped persons Health and Human Health Service hearing hospital Human Services ICRC institution means ment National notice notify operation organization paragraph participation partment party payment period procedures procurement program or activity prohibited proposed purpose pursuant quired real property received recipient records regulations request responsible section 504 Single Audit sion Social Security Act specific Stat statute subgrantee submit Subpart tion Title title IX unless violation
Popular passages
Page 342 - Each of the matters of which an admission is requested shall be deemed admitted unless, within a period designated in the request, not less than 10 days after service thereof or within such shorter or longer time as the court may allow on motion and notice, the party to whom the...
Page 38 - ... (4) to the Bureau of the Census for purposes of planning or carrying out a census or survey or related activity pursuant to the provisions of title 13; (5) to a recipient who has provided the agency with advance adequate written assurance that the record will be used solely as a statistical research or reporting record, and the record is to be transferred in a form that is not individually identifiable...
Page 307 - Although relevant, evidence may be excluded if its probative value is substantially outweighed by the danger of unfair prejudice, confusion of the issues, or misleading the jury, or by considerations of undue dela'y, waste of time, or needless presentation of cumulative evidence.
Page 175 - ... and receives in advance a written determination made by such official that the interest is not so substantial as to be deemed likely to affect the integrity of the services which the Government may expect from...
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 124 - 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 323 - State or political subdivision, any public or private agency, institution, or organization, or 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. (j) The term "primary recipient...
Page 125 - ... 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 116 - Research involving the collection or study of existing data, documents, records, pathological specimens, or diagnostic specimens, if these sources are publicly available or if the information is recorded by the investigator in such a manner that subjects cannot be identified, directly or through identifiers linked to the subjects.
Page 316 - Each recipient shall keep such records and submit to the responsible Department official or his designee timely, complete and accurate compliance reports at such times, and in such form and containing such information, as the responsible Department official or his designee may determine to be necessary to enable him to ascertain whether the recipient has complied or is complying with this part.