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Expedited Review Criteria
Certain types of research protocols may be eligible for review under expedited review procedures. The research must involve no more than minimal risk and fit one or more of the categories for expedited review procedures as specified in the regulations [45 CFR 46.110 and 21 CFR 56.110] and described below.

[DOC File]§21 - Veterans Affairs
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(c) Time limit for filing a claim for an extended period of eligibility under 10 U.S.C. chapter 1606, or 38 U.S.C. chapter 30, 32, 33, or 35. VA must receive a claim for an extended period of eligibility provided by §21.3047, §21.5042, §21.7051, §21.7551, or §21.9535 by the later of the following dates:

[DOC File]ENVIRONMENTAL PROTECTION AGENCY
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[See Inspection Log and Schedule in Attachment 3.1] [§§112.8(c)(6) and 112.12(c)(6)] For bulk storage containers that are subject to 21 CFR part 110 which are shop-fabricated, constructed of austenitic stainless steel, elevated and have no external insulation, formal visual inspection is conducted on a regular schedule.

[DOC File]CFR Part 21 - Certification procedures for products and parts
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Advisory Circular 20-110 contains a list of Technical Standard Orders that may be used to obtain approval. Copies of the Advisory Circular may be obtained from the U.S. Department of Transportation, Publication Section (M-443.1), Washington, D.C. 20590; ... CFR Part 21 - Certification procedures for products and parts ...

[DOCX File]South Carolina Legislature Online
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The regulations are based on Title 21, Part 110, Current Good Manufacturing Practice in Manufacturing, Packing, or Holding Human Food of the Code of Federal Regulations (21 CFR Part 110). The Department of Health and Environmental Control (“Department”) last amended R.6136 in 2004.

[DOC File]Request for Expedited Review
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Authority: Title 45 Code of Federal Regulations (CFR) 46.110, 38 CFR 16.110, and 21 CFR 56.110.) An expedited review procedure consists of a review of research involving human subjects by the IRB chairperson or by one or more experienced reviewers designated by the chairperson from among members of the IRB in accordance with the requirements set forth in 38 CFR 16.110.

[DOC File]ENVIRONMENTAL PROTECTION AGENCY
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[See Inspection Log and Schedule in Attachment 3.1] [§§112.8(c)(6) and 112.12(c)(6)] For bulk storage containers that are subject to 21 CFR part 110 which are shop-fabricated, constructed of austenitic stainless steel, elevated and have no external insulation, formal visual inspection is conducted on a regular schedule.

[DOC File]FDA Regulation: 21 – CFR – 314 New Drug Application
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(c) References in this part to regulations in the Code of Federal . Regulations are to chapter I of title 21, unless otherwise noted. [50 FR 7493, Feb. 22, 1985, as amended at 57 FR 17981, Apr. 28, 1992; 64 . FR 401, Jan. 5, 1999] Sec. 314.2 Purpose. The purpose of this part is to establish an efficient and thorough

[DOC File]CHAPTER 1
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24 CFR, part 1 Title VI of the Civil Rights Act of 1964. 24 CFR, part 8 Section 504 of the Rehabilitation Act of 1973. 24 CFR, part 100 et seq Fair Housing Act. 24 CFR, part 146 Age Discrimination Act of 1975. 24 CFR 200.600 Affirmative Fair Marketing Regulations

[DOC File][Code of Federal Regulations]
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[Title 21, Volume 1] [Revised as of April 1, 2003] From the U.S. Government Printing Office via GPO Access [CITE: 21CFR1] TITLE 21--FOOD AND DRUGS. CHAPTER I--FOOD AND DRUG ADMINISTRATION. DEPARTMENT OF HEALTH AND HUMAN SERVICES. PART 1--GENERAL ENFORCEMENT REGULATIONS. Subpart A--General Provisions. Sec. 1.1 General.

[DOC File]Institutional Review Board & Human Research Management
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By signing below, I agree to conduct the investigation in accordance with the signed agreement with the sponsor, the investigational plan, 21 CFR Part 812 or 21 CFR Part 312, as applicable and other applicable FDA regulations, and conditions of approval imposed by Salus IRB or FDA.

[DOCX File]South Carolina Legislature Online
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The Department of Health and Environmental Control (Department) last amended R.6132 in 2004 and R.6154 in 2008. Earlier this year, 21 CFR Part 110, Current Good Manufacturing Practice in Manufacturing, Packing, or Holding Human Food, was replaced with 21 CFR Part 117, Current Good Manufacturing Practice, Hazard Analysis, and RiskBased Preventive Controls for Human Food.

[DOCX File]RESEARCH CATEGORIES - The University of Texas at Tyler
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21 CFR 56.110. (B) The categories in this list apply regardless of the age of subjects, except as noted. ... (21 CFR Part 812) is not required; or (ii) the medical device is cleared/approved for marketing and the medical device is being used in accordance with its cleared/approved labeling.

[DOC File][Code of Federal Regulations]
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with this part is intended to protect the rights and welfare of human . subjects involved in such investigations. (b) References in this part to regulatory sections of the Code of . Federal Regulations are to chapter I of title 21, unless otherwise . noted. [46 FR 8975, Jan. 27, 1981, as amended at 64 FR 399, Jan. 5, 1999; 66 FR . 20599, Apr ...

21 cfr part 110