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as further defined by regulation (21 CFR 1308.11 through 1308.15);

Conviction means a finding of guilt (including a plea of nolo contendere) or imposition of Sentence, or both, by any judicial body charged with the responsibility to determine violations of the Federal or State Criminal drug StatuteS;

Criminal drug statute means a Federal or non-Federal criminal Statute involving the manufacture, distribution, dispensing, use, or possession of any controlled Substance;

Employee means the employee of a grantee directly engaged in the performance of work under a grant, including: (i) All direct charge employees; (ii) All indirect charge employees unless their impact or involvement is insignificant to the performance Of the grant; and, (iii) Temporary perSonnel and Consultants who are directly engaged in the performance of work under the grant, and who are on the grantee’s payroll. This definition does not include workers not on the payroll of the grantee (e.g., volunteers, even if used to meet a matching requirement; Consultants or independent contractors not on the grantee’s payroll; or employees of Subrecipients or Subcontractors in Covered workplaces).

Certification Regarding Drug-Free Workplace Requirements

Alternate I. (Grantees Other Than IndividualS)

A. The grantee certifies that it will or will continue to provide a drug-free workplace by:

(a) Publishing a Statement notifying employees that the unlawful manufacture, distribution, dispensing, possession, or use of a controlled Substance is prohibited in the grantee’s workplace and Specifying the actions that will be taken against employees for violation of Such prohibition;

(b) Establishing an ongoing drug-free

awareness program to inform employees about— (1) The dangers of drug abuse in the workplace; (2) The grantee’s policy of maintaining a drug-free workplace; (3) Any available drug counseling, rehabilitation, and employee a SSiStance programS; and (4) The penalties that may be imposed upon employees for drug abuse violations OCCurring in the workplace; (C) Making it a requirement that each employee to be engaged in the performance of the grant be given a copy of the Statement required by paragraph (a); (d) Notifying the employee in the statement required by paragraph (a) that, as a condition of employment under the grant, the employee will—

(1) Abide by the terms of the Statement; and (2) Notify the employer in writing of his or her conviction for a violation of a criminal drug Statute occurring in the workplace no later than five calendar days after such conviction; (e) Notifying the agency in writing, within ten Calendar days after receiving notice under paragraph (d)(2) from an employee or Otherwise receiving actual notice of Such conviction. Employers of convicted employ– ees must provide notice, including position title, to every grant Officer or other designee on whose grant activity the Convicted employee was working, unless the Federal agency has designated a Central point for the receipt of such notices. Notice Shall include the identification number(s) of each affected grant; (f) Taking one of the following actions, within 30 Calendar days of receiving notice under paragraph (d)(2), with respect to any employee who is So convicted— (1) Taking appropriate personnel action against Such an employee, up to and including termination, consistent with the requirements of the Rehabilitation Act of 1973, aS amended; Or (2) Requiring Such employee to participate Satisfactorily in a drug abuse assistance Or rehabilitation program approved for Such purposes by a Federal, State, or local health, law enforcement, or other appropriate agenCy; (g) Making a good faith effort to Continue to maintain a drug-free workplace through implementation of paragraphs (a), (b), (c), (d), (e) and (f). B. The grantee may insert in the Space provided below the site(s) for the performance of work done in Connection with the Specific grant.

Place of Performance (Street address, city, County, State, Zip Code)

Check D if there are workplaces on file that are not identified here.


(a) The grantee Certifies that, as a Condition of the grant, he or she will not engage in the unlawful manufacture, distribution, dispensing, possession, or use of a controlled substance in conducting any activity with the grant;

(b) If convicted of a criminal drug offense resulting from a violation occurring during the conduct of any grant activity, he or She will report the conviction, in writing, within 10 calendar days of the conviction, to every grant officer or other designee, unless the Federal agency designates a central point for the receipt of such notices. When notice is made to such a central point, it shall include the identification number(s) of each affected grant.

[55 FR 21690, 21693, May 25, 1990]


Sec. 27.101 To what does this policy apply? 27.102 Definitions. 27.103 ASSuring compliance with this policy—research conducted or Supported by any Federal Department or Agency. 27.104–27.106 [Reserved] 27.107 IRB membership. 27.108 IRB functions and operations. 27.109 IRB review of research. 27.1.10 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research. 27.111 Criteria for IRB approval of research. 27.112 Review by institution. 27.113 Suspension or termination of IRB approval of research. 27.114 Cooperative research. 27.115 IRB records. 27.116 General requirements for informed COnSent. 27.117 Documentation of informed Consent. 27.118 Applications and proposals lacking definite plans for involvement of human SubjectS. 27.119 Research undertaken without the intention of involving human SubjectS. 27.120 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department or Agency. 27.121 [Reserved] 27.122 USe of Federal fundS. 27.123 Early termination of research Support: Evaluation of applications and proposals. 27.124 ConditionS.

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personnel, except that each department Or agency head may adopt such procedural modifications as may be appropriate from an administrative standpoint. It also includes research conducted, supported, or otherwise subject to regulation by the federal government Outside the United States. (1) Research that is conducted or Supported by a federal department or agency, whether or not it is regulated as defined in $27.102(e), must comply with all sections of this policy. (2) Research that is neither Conducted nor supported by a federal department or agency but is subject to regulation as defined in $27.102(e) must be reviewed and approved, in compliance with $27.101, $27.102, and $27.107 through $27.117 of this policy, by an institutional review board (IRB) that operates in accordance with the pertinent requirements of this policy. (b) Unless otherwise required by department or agency heads, research activities in which the only involvement of human subjects will be in one or more of the following categories are exempt from this policy: (1) Research Conducted in established Or Commonly accepted educational settings, involving normal educational practices, such as (i) research on regular and Special education instructional Strategies, Or (ii) research. On the effectiveness of Or the Comparison annong instructional techniques, Curricula, or Classroom management methods. (2) Research involving the use of eduCational testS (Cognitive, diagnostic, aptitude, achievement), Survey procedures, interview procedures or observation of public behavior, unless: (i) Information obtained is recorded in such a manner that human subjects can be identified, directly or through identifiers linked to the Subjects; and (ii) any disclosure of the human subjects’ responses OutSide the research could reasonably place the subjects at risk of criminal or civil liability or be damaging to the Subjects’ financial Standing, employability, or reputation. (3) Research involving the use of educational tests (cognitive, diagnostic, aptitude, achievement), Survey procedures, interview procedures, or obserVation of public behavior that is not

exempt under paragraph (b)(2) of this section, if: (i) The human subjects are elected or appointed public officials or candidates for public office; or (ii) federal statute(s) require(s) without exception that the confidentiality of the personally identifiable information will be maintained throughout the research and thereafter. (4) 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. (5) Research and demonstration projects which are conducted by or subject to the approval of department or agency heads, and Which are designed to study, evaluate, or otherwise exam1116. (i) Public benefit or service programs; (ii) procedures for obtaining benefits or services under those programs; (iii) possible changes in Or alternatives to those programs Or procedures; Or (iv) possible changes in methOds or levels Of payment for benefits or Services under those programs. (6) Taste and food quality evaluation and consumer acceptance studies, (i) if wholesome foods without additives are consumed or (ii) if a food is consumed that contains a food ingredient at or below the level and for a use found to be safe, or agricultural chemical or environmental contaminant at or below the level found to be safe, by the Food and Drug Administration or approved by the Environmental Protection Agency or the Food Safety and Inspection Service of the U.S. Department of Agriculture. (c) Department or agency heads retain final judgment as to whether a particular activity is covered by this policy. (d) Department or agency heads may require that specific research activities or classes of research activities conducted, Supported, or otherwise subject to regulation by the department or agency but not otherwise covered by this policy, comply with some or all of the requirements of this policy.


(e) Compliance with this policy reQuires Compliance with pertinent federal laws or regulations which provide additional protections for human subjects. (f) This policy does not affect any State or local laws or regulations which may otherwise be applicable and which additional protections for human subjects. (g) This policy does not affect any foreign laws or regulations which may Otherwise be applicable and which provide additional protections to human Subjects of research. (h) When research covered by this policy takes place in foreign countries, procedures normally followed in the foreign countries to protect human Subjects may differ from those set forth in this policy. [An example is a foreign institution which complies With guidelines consistent with the World Medical Assembly Declaration (Declaration of Helsinki annended 1989) issued either by sovereign states or by an Organization whose function for the protection of human research subjects is internationally recognized.] In these Circumstances, if a department or agency head determines that the procedures prescribed by the institution afford protections that are at least equivalent to those provided in this policy, the department or agency head may approve the substitution of the foreign procedures in lieu of the procedural requirements provided in this policy. Except when otherwise required by statute, Executive Order, or the department or agency head, notices of these actions as they occur will be published in the FEDERAL REGISTER or will be otherwise published as provided in department or agency procedures. (i) Unless otherwise required by law, department or agency heads may waive the applicability of some or all of the provisions of this policy to specific reSearch activities Or Classes of research activities otherwise COvered by this policy. Except when otherwise required by statute or Executive Order, the department or agency head shall forward advance notices of these actions to the Office for Protection from Research Risks, Department of Health and Human Services (HHS), and shall also publish them in the FEDERAL REGISTER or in such other manner as provided in department or agency procedures.1

[56 FR 28012 and 28019, June 18, 1991, 56 FR 29756, June 28, 1991]

$27.102 Definitions.

(a) Department or agency head means the head of any federal department or agency and any other officer or employee of any department or agency to whom authority has been delegated. (b) Institution means any public or private entity or agency (including federal, state, and other agencies). (c) 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 they are Conducted Or supported under a program which is considered research for other purposes. For example, some demonstration and service programs may include research activities. (e) Research Subject to regulation, and Similar terms are intended to encompass those research activities for which a federal department or agency has Specific responsibility for regulating as a research activity, (for example, Investigational New Drug requirements administered by the Food and Drug Ad

1 Institutions with HHS-approved a SSurances on file will abide by provisions of title 45 CFR part 46 subparts A–D. Some of the other Departments and Agencies have incorporated all provisions of title 45 CFR part 46 into their policies and procedures as well. However, the exemptions at 45 CFR part 46.101(b) do not apply to research involving prisoners, fetuses, pregnant women, or human in vitro fertilization, Subparts B and C. The exemption at 45 CFR part 46.101(b)(2), for research involving Survey Or interview procedures or observation of public behavior, does not apply to research with children, subpart D, except for research involving observations of public behavior when the investigator(s) do not participate in the activities being observed.

ministration). It does not include reSearch activities which are incidentally regulated by a federal department or agency solely as part of the department’s or agency’s broader responsibility to regulate certain types of activities whether research or non-research in nature (for example, Wage and Hour requirements administered by the Department of Labor). (f) Human Subject means a living individual about whom an investigator (whether professional or student) conducting research obtains (1) data through intervention or interaction with the individual, or (2) identifiable private information.

Intervention includes both physical procedures by which data are gathered (for example, venipuncture) and manipulations of the subject or the subject’s environment that are performed for reSearch purposes. Interaction includes COmnunication Or interpersonal Contact between investigator and subject. “Private information” includes information about behavior that occurs in a Context in which an individual can reasonably expect that no observation or recording is taking place, and information which has been provided for speCific purposes by an individual and which the individual can reasonably expect will not be made public (for example, a medical record). Private information must be individually identifiable (i.e., the identity of the subject is or may readily be ascertained by the investigator Or a SSOciated with the information) in order for obtaining the information to Constitute research involving human subjects. (g) IRB means an institutional review board established in accord with and for the purposes expressed in this pol1Cy. (h) IRB approval means the determination of the IRB that the research has been reviewed and may be conducted at an institution within the constraints set forth by the IRB and by Other institutional and federal requirement.S. (i) 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. (j) Certification means the Official notification by the institution to the Supporting department or agency, in acCordance with the requirements of this policy, that a research project or activity involving human subjects has been reviewed and approved by an IRB in acCordance with an approved assurance.

$27.103 Assuring compliance with this policy—research conducted or supported by any Federal Department or Agency. (a) Each institution engaged in research which is covered by this policy and which is conducted or supported by a federal department or agency shall provide written assurance satisfactory to the department or agency head that it will Comply with the requirements set forth in this policy. In lieu of requiring Submission of an assurance, individual department or agency heads shall accept the existence of a current aSSurance, appropriate for the research in question, on file with the Office for Protection from Research Risks, HHS, and approved for federal wide use by that office. When the existence of an HHS-approved assurance is accepted in lieu of requiring submission of an asSurance, reportS (except, Certification) required by this policy to be made to department and agency heads shall also be made to the Office for Protection from Research Risks, HHS. (b) Departments and agencies will conduct or support research covered by this policy only if the institution has an a SSurance approved as provided in this section, and only if the institution has certified to the department or agency head that the research has been reviewed and approved by an IRB provided for in the assurance, and will be Subject to continuing review by the IRB. Assurances applicable to federally Supported or conducted research shall at a minimum include: (1) A statement of principles governing the institution in the discharge of its responsibilities for protecting the rights and welfare of human subjects of research conducted at or sponsored by the institution, regardless of whether the research is subject to federal regu

lation. This may include an appropriate existing code, declaration, or Statement of ethical principles, or a Statement formulated by the institution itself. This requirement does not preempt provisions of this policy appliCable to department- or agency-supported or regulated research and need not be applicable to any research exempted or waived under $27.101 (b) or (i). (2) Designation of one or more IRBs established in accordance with the reQuirements of this policy, and for which provisions are made for meeting Space and sufficient staff to support the IRB's review and recordkeeping duties. (3) A list of IRB members identified by name; earned degrees; representative CapaCity; indications of experience Such as board certifications, licenses, etc., Sufficient to describe each member’s chief anticipated contributions to IRB deliberations; and any employment or other relationship between each member and the institution; for example: full-time employee, part-time employee, member of governing panel or board, stockholder, paid or unpaid Consultant. Changes in IRB memberShip shall be reported to the department or agency head, unless in accord with $27.103(a) of this policy, the existence of an HHS-approved assurance is accepted. In this case, change in IRB membership shall be reported to the Office for Protection from Research Risks, HHS. (4) Written procedures which the IRB will follow (i) for conducting its initial and continuing review of research and for reporting its findings and actions to the investigator and the institution; (ii) for determining which projects require review more often than annually and which projects need verification from Sources other than the investigators that no material changes have ocCurred Since previous IRB review; and (iii) for ensuring prompt reporting to the IRB of proposed changes in a reSearch activity, and for ensuring that Such changes in approved research, during the period for which IRB approval has already been given, may not be initiated without IRB review and approval except when necessary to

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