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40 CFR 26.103 · Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
40 CFR 26.104 · Exempt research.
40 CFR 26.105-26.106 · §§ 26.105-26.106 [Reserved]
40 CFR 26.107 · IRB membership.
40 CFR 26.108 · IRB functions and operations.
40 CFR 26.109 · IRB review of research.
40 CFR 26.110 · Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
40 CFR 26.111 · Criteria for IRB approval of research.
40 CFR 26.112 · Review by Institution
40 CFR 26.113 · Suspension or Termination of IRB Approval of Research.
40 CFR 26.114 · Cooperative Research.
40 CFR 26.115 · IRB Records.
40 CFR 26.116 · General Requirements for Informed Consent.
40 CFR 26.117 · Documentation of informed consent.
40 CFR 26.118 · Applications and proposals lacking definite plans for involvement of human subjects.
40 CFR 26.119 · Research undertaken without the intention of involving human subjects.
40 CFR 26.120 · Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
40 CFR 26.121 · [Reserved]
40 CFR 26.122 · Use of Federal funds.
40 CFR 26.123 · Early termination of research support: Evaluation of applications and proposals.
40 CFR 26.124 · Conditions.
40 CFR 26.201 · To what does this subpart apply?
40 CFR 26.202 · Definitions.
40 CFR 26.203 · Prohibition of research conducted or supported by EPA involving intentional exposure of any human subject who is a pregnant woman (and therefore her fetus), a nursing woman, or child.
40 CFR 26.301 · To what does this subpart apply?
40 CFR 26.302 · Definitions.
40 CFR 26.303 · Duties of IRBs in connection with observational research involving pregnant women and fetuses.
40 CFR 26.304 · Additional protections for pregnant women and fetuses involved in observational research.
40 CFR 26.305 · Protections applicable, after delivery, to the placenta, the dead fetus, or fetal material.
40 CFR 26.401 · To what does this subpart apply?
40 CFR 26.402 · Definitions.
40 CFR 26.403 · IRB duties.
40 CFR 26.404 · Observational research not involving greater than minimal risk.
40 CFR 26.405 · Observational research involving greater than minimal risk but presenting the prospect of direct benefit to the individual subjects.
40 CFR 26.406 · Requirements for permission by parents or guardians and for assent by children.
40 CFR 26.1101 · To what does this subpart apply?
40 CFR 26.1102 · Definitions.
40 CFR 26.1103-26.1106 · §§ 26.1103-26.1106 [Reserved]
40 CFR 26.1107 · IRB membership.
40 CFR 26.1108 · IRB functions and operations.
40 CFR 26.1109 · IRB review of research.
40 CFR 26.1110 · Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
40 CFR 26.1111 · Criteria for IRB approval of research.
40 CFR 26.1112 · Review by institution.
40 CFR 26.1113 · Suspension or termination of IRB approval of research.
40 CFR 26.1114 · Cooperative research.
40 CFR 26.1115 · IRB records.
40 CFR 26.1116 · General requirements for informed consent.
40 CFR 26.1117 · Documentation of informed consent.
40 CFR 26.1118-26.1122 · §§ 26.1118-26.1122 [Reserved]
40 CFR 26.1123 · Early termination of research.
40 CFR 26.1124 · [Reserved]
40 CFR 26.1125 · Prior submission of proposed human research for EPA review.
40 CFR 26.1201 · To what does this subpart apply?
40 CFR 26.1202 · Definitions.
40 CFR 26.1203 · Prohibition of research involving intentional exposure of any human subject who is a pregnant woman (and therefore her fetus), a nursing woman, or a child.
40 CFR 26.1301 · To what does this subpart apply?
40 CFR 26.1302 · Definitions.
40 CFR 26.1303 · Submission of information pertaining to ethical conduct of completed human research.
40 CFR 26.1501 · To what does this subpart apply?
40 CFR 26.1502 · Lesser administrative actions.
40 CFR 26.1503 · Disqualification of an IRB or an institution.
40 CFR 26.1504 · Public disclosure of information regarding revocation.
40 CFR 26.1505 · Reinstatement of an IRB or an institution.
40 CFR 26.1506 · Debarment.
40 CFR 26.1507 · Actions alternative or additional to disqualification.
40 CFR 26.1601 · To what does this subpart apply?
40 CFR 26.1602 · Definitions.
40 CFR 26.1603 · EPA review of proposed human research.
40 CFR 26.1604 · EPA review of completed human research.
40 CFR 26.1605 · Operation of the Human Studies Review Board.
40 CFR 26.1606 · Human Studies Review Board review of proposed human research.
40 CFR 26.1607 · Human Studies Review Board review of completed human research.
40 CFR 26.1701 · To what does this subpart apply?
40 CFR 26.1702 · Definitions.
40 CFR 26.1703 · Prohibitions applying to all research subject to this subpart.
40 CFR 26.1704 · Prohibition of reliance on unethical human research with non-pregnant, non-nursing adults.
40 CFR 26.1705 · Prohibition of reliance on unethical human research with non-pregnant, non-nursing adults initiated after April 7, 2006.
40 CFR 26.1706 · Criteria and procedure for decisions to protect public health by relying on otherwise unacceptable research.
40 CFR 27.1 · Basis and purpose.
40 CFR 27.2 · Definitions.
40 CFR 27.3 · Basis for civil penalties and assessments.
40 CFR 27.4 · Investigation.
40 CFR 27.5 · Review by the reviewing official.
40 CFR 27.6 · Prerequisites for issuing a complaint.
40 CFR 27.7 · Complaint.
40 CFR 27.8 · Service of complaint.
40 CFR 27.9 · Answer.
40 CFR 27.10 · Default upon failure to file an answer.
40 CFR 27.11 · Referral of complaint and answer to the presiding officer.
40 CFR 27.12 · Notice of hearing.
40 CFR 27.13 · Parties to the hearing.
40 CFR 27.14 · Separation of functions.
40 CFR 27.15 · Ex parte contacts.
40 CFR 27.16 · Disqualification of the reviewing official or presiding officer.
40 CFR 27.17 · Rights of parties.
40 CFR 27.18 · Authority of the presiding officer.
40 CFR 27.19 · Prehearing conferences.
40 CFR 27.20 · Disclosure of documents.
40 CFR 27.21 · Discovery.