Research Involving Human Subjects: Difference between revisions

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Policy 209
Policy 209
== Introduction ==
== Purpose ==
1.1 This policy provides authority to the Institutional Review Board (hereinafter “IRB”) to provide ethical and regulatory oversight for research involving human subjects conducted by Appalachian State University, its faculty, staff, students and visitors.


1.2 The University is committed to protecting the rights and welfare of human subjects participating in research projects. Therefore, the University has created an Institutional Review Board (“IRB”) to ensure protection of human subject rights and welfare during any research activity. The IRB acts according to policies set forth by the United States Department of Health and Human Services Public Health Service Act as amended. Compliance with these federal regulations not only safeguards human subjects and the institution sponsoring the research project, but also protects the Principal Investigator.
This policy provides authority to the Institutional Review Board (hereinafter “IRB”) to provide ethical
and regulatory oversight for research involving human subjects conducted by Appalachian State
University, its faculty, staff, students and visitors.


== Scope ==
== Scope ==
2.1 This policy applies to all faculty, staff, students and any other individual engaged in research involving human subjects on the campus of the University, through funding provided by the University, on behalf of the University or in conjunction with University employees or students.
 
This policy applies to all faculty, staff, students and any other individual engaged in research involving
human subjects on the campus of the University, through funding provided by the University, on behalf
of the University or in conjunction with University employees or students.


== Definitions  ==
== Definitions  ==


=== Anonymity ===
=== Anonymity ===
:means that the identity of a subject cannot be matched to his/her response either directly through identifiers or by “linked” or “coded” responses.
:Means that the identity of subjects cannot be matched to their responses either directly through identifiers or by "linked" or "coded" responses.


=== Confidentiality ===
=== Confidentiality ===
:means not disclosing individually identifiable information received from a human subject to others in a manner inconsistent with the understanding of the original Informed Consent agreement.
:Means not disclosing individually identifiable information received from a human subject to others in a manner inconsistent with the understanding of the original Informed Consent agreement.


=== Data Collection ===
=== Data Collection ===
:means any research procedure that is intended to elicit from or record the actions, reactions, attitudes, and/or behavioral manifestations of human subjects participating in a research project.
:Means any research procedure that is intended to elicit from or record the actions, reactions, attitudes, and/or behavioral manifestations of human subjects participating in a research project.


=== Exempt Research ===
=== Exempt Research ===
means human subject research activities which are minimal risk in nature and fall into one or more of the federally defined exempt research categories.
:Means human subject research activities which are minimal risk in nature and fall into one or more of the federally defined exempt research categories.
 
=== Expedited Review ===
=== Expedited Review ===
:means a review by the IRB Chair or designee of research proposals which involve minimal risk or no-risk.
:Means a review by the IRB Chair or designee of research proposals which involve minimal risk or no-risk.


=== Full IRB Review ===
=== Full IRB Review ===
:means the review of proposals conducted during a convened IRB meeting at which a quorum has been established.
:Means the review of proposals conducted during a convened IRB meeting at which a quorum has been established.


=== Human Subject ===
=== Human Subject ===
:means a living individual about whom a researcher (whether professional or student) conducting research that (i) Obtains information or biospecimens through intervention or interaction with the individual, and uses, studies, or analyzes the information or biospecimens; or (ii) Obtains, uses, studies, analyzes, or generates identifiable private information or identifiable bio-specimens.
:Means a living individual about whom a researcher (whether professional or student) conducting research that (i) Obtains information or biospecimens through intervention or interaction with the individual, and uses, studies, or analyzes the information or biospecimens; or (ii) Obtains, uses, studies, analyzes, or generates identifiable private information or identifiable bio-specimens.


=== Informed Consent ===
=== Informed Consent ===
:means the voluntary agreement by an individual or an individual's legally authorized representative to participate in a particular study without any element of force, fraud, deceit, duress, or any other form of constraint or coercion. Valid consent requires voluntary action, competence, informed decision, and comprehension of terminology.
:Means the voluntary agreement by an individual or an individual's legally authorized representative to participate in a particular study without any element of force, fraud, deceit, duress, or any other form of constraint or coercion. Valid consent requires voluntary action, competence, informed decision, and comprehension of terminology.


=== IRB ===
=== IRB ===
:means the University’s institutional review board.
:Means the University’s institutional review board.
 
=== Minimal Risk ===
=== Minimal Risk ===
:means that the probability and magnitude of harm(s) or discomfort(s) anticipated in the research are not greater than those ordinarily encountered in daily life or during the performance of routine physical or psychological examinations.
:Means that the probability and magnitude of harm(s) or discomfort(s) anticipated in the research are not greater than those ordinarily encountered in daily life or during the performance of routine physical or psychological examinations.


=== Research ===
=== Research ===
:means a systematic investigation, including research development, testing, and evaluation, designed to develop or contribute to generalizable knowledge. Activities that meet this definition constitute research for purposes of this policy, whether or not they are conducted or supported under a program that is considered research for other purposes. For example, some demonstration and service programs may include research activities.  
:Means a systematic investigation, including research development, testing, and evaluation, designed to develop or contribute to generalizable knowledge. Activities that meet this definition constitute research for purposes of this policy, whether or not they are conducted or supported under a program that is considered research for other purposes. For example, some demonstration and service programs may include research activities.


=== University ===
=== University ===
:means Appalachian State University
:Means Appalachian State University


=== Vulnerable Populations ===
=== Vulnerable Populations ===
:means human subjects that are children, prisoners, pregnant persons, or any population that may be relatively or absolutely incapable of protecting their interests through the informed consent process.
:Means human subjects that are children, prisoners, pregnant persons, or any population that may be relatively or absolutely incapable of protecting their interests through the informed consent process.


== Policy and Procedure Statements  ==
== Policy and Procedure Statements  ==
=== The Institutional Review Board (IRB) and Its Actions ===
4.1.1 In reviewing research proposals, the IRB has the authority to approve, require modifications in, defer, disapprove or terminate any research involving human subjects conducted under Appalachian State University’s auspices.


4.1.2 If at any time, the Board becomes aware of:
=== Roles and Responsibilities ===
#unanticipated problems involving risks to subjects, or
#other serious or continuing noncompliance with 45 CFR 46 or determinations of the Board, including ongoing human subject research which has not been reviewed by the Board,it may request a meeting with the PI and/or suspend the research until the problem can be further evaluated. Under these circumstances, the Authorized Institutional Official (the Dean of Graduate Studies and Research) must be made aware of the situation immediately, and he/she will be advised of any further sanctions subsequently recommended by the Board.


4.1.3 In these circumstances, the Board may impose sanctions on an individual by suspending the individual's right to conduct or supervise research involving human subjects, taking possession of the data collected by the non-compliant individual, withholding or revoking academic credit to a student researcher, and recommending discipline of a faculty member by the University. This list is provided by way of example only, and is not intended and should not be construed as exhaustive, in that individual situations may call for specific actions and remedies not identified herein.
==== Protection of Research Subjects ====
The primary responsibility for the responsible conduct of research shall reside with the investigators who are conducting the research. However, other persons not involved directly share in the responsibility to establish and maintain an atmosphere where respect for the rights of individuals and compliance with applicable regulations is the standard.


=== The Review Process ===
==== Vice Provost for Research ====
4.2.1 The IRB reviews protocols for research in accordance with federal regulations governing research with human subjects. The Board may also apply such codes of professional ethics as it deems appropriate. These additional codes may or may not be addressed in federal documents. It is the policy of Appalachian State University that in order for any research protocol to be approved, the Board must determine that all of the following requirements are satisfied:
The Chancellor has designated the University’s Vice Provost for Research ("VPR") as the authorized Institutional Officer ("IO") with responsibility for the University’s program for the protection of human subjects.
#Risks to subjects are minimized and are reasonable in relation to anticipated benefits of the research,
#Selection of subjects is equitable given the purposes and the setting of the research,
#Appropriate informed consent will be sought from each subject or the subject's legally authorized representative, and such consent will be appropriately documented (see Informed Consent Guidelines below),
#The research plan makes appropriate provision for monitoring the data collected to insure the safety of subjects,
#Appropriate provisions are made to protect the privacy of subjects and to maintain the confidentiality of data, and
#Where some or all of the subjects are likely to be vulnerable to coercion or undue influence, appropriate additional safeguards have been included to protect the rights and welfare of these subjects.


4.2.2 The IRB may process a protocol in one of three ways:
==== Members of IRB ====
#By exemption certification
4.1.3.1 The IRB shall report to the IO and consist of a minimum of five members, including:
#By expedited review
# One member from a scientific area; and
#By full review
# One member from a nonscientific area; and
# One member unaffiliated with the University; and
# Other additional members to provide expertise in research areas commonly employing human subjects, or expertise with unique or vulnerable populations to ensure ethical treatment of subjects; and
# The IRB Administrator, as an ex officio non-voting member.
4.1.3.2 The Chancellor shall appoint all members of the IRB for a term of one to three years and shall designate a Chair.


4.2.3 Any research protocol which does not fall under the category definitions of exempted or expedited research as outlined below, or any protocol as specifically requested by the Board, shall undergo full review.
==== Office of Research Protections ====
The Office of Research Protections provides administrative support and leadership to the IRB, and is responsible for the interpretation and implementation of this policy, as well as addressing non-compliance with this policy. The Office of Research Protection is responsible for:


4.2.4 Upon review by the Board, the office of the IRB Administrator shall notify the PI by letter and/or email of the Board’s decisions, and conditions which must be met, if approval is to be awarded. Approval will not be granted until all specified conditions are met. The letter shall also
# Developing procedures to facilitate the review of human subjects research and to maintain compliance with federal regulations related to the protection of human subjects,
#Advise the PI to notify the IRB if there are any subsequent changes proposed in the research protocol. No changes may be initiated without IRB review and approval.
# Developing procedures and guidelines for the IRB and University community related to the protection of human subjects under this policy,
#Indicate the period for which approval is valid (1 year, in most cases).
# Providing federal and state regulatory updates to the IRB and University Community, and
#Require the PI to make an application for annual review should the study extend beyond the initial approval expiration date.
# Acting as liaison with federal regulators when necessary.
#Direct that during the course of the research, should an adverse event occur which threatens the health, safety or emotional well-being of a participant, or which increases the risks to subjects from that described in the approval documents for the project, the PI must suspend the research immediately and report the incident to the IRB Administrator. The IRB Administrator will investigate and determine the course of action to follow.


=== Categories of Review ===
=== IRB Oversight ===
==== Exempt Research ====
4.2.1  Any research involving human subjects, including internally funded, externally funded or unfunded research that involves University faculty, staff or students or is supported by or conducted on the University campus, must be reviewed and approved by the IRB prior to soliciting human subject participants or collecting any data from any human subject.
a. Certain categories of research protocols may be exempt from review. Only the IRB Administrator or IRB Associate Administrator is authorized to determine which protocols may be subject to limited review or may be exempt from review by the Board. Investigators who believe that their research meets the following criteria may request exempt status for their study when it is submitted to the Board, and list the justification. The IRB reserves the authority to require proposal modifications regarding human subject protection before approving the research as exempted from the requirements of the Common Rule.


b. Note that the exemption DOES NOT APPLY when the research activities include:
4.2.2 The IO has the authority to rely on another institution’s IRB approval for collaborative activities where human subject protections are the responsibility of the collaborating intuition’s human subjects program.
#Prisoners, fetuses, pregnant women or human in-vitro fertilization.
#The review of medical records when the information is recorded in such a way that subjects can be identified, directly or through identifiers linked to the subjects.
#Techniques which expose the subject to more than minimal risk.
#The deception of the subject.


c. The federal categories of research eligible for exemption certification are as follows:
=== Review Requirements ===
#Research conducted in established or commonly accepted educational settings, involving normal education practices, such as (a) research on regular and special education instructional strategies, or (b) research on the effectiveness of or the comparison among instructional techniques, curricula, or classroom management methods.
4.3.1 The IRB shall only approve research protocols that satisfy all of the following requirements:
#Research involving the use of educational tests (cognitive, diagnostic, aptitude, achievement), surveys, interviews or observation of public behavior, unless: (i) information obtained is recorded in such a manner that participants can be identified, directly or through identifiers linked to the subjects; and (ii) any disclosure of an individual’s response(s) outside of the research setting could reasonably place the subject at risk of criminal or civil liability or be damaging to the subjects' financial standing, employability, or reputation. Surveys or interviews which include minors as subjects are not included in this exempt category.
# Any risk(s) to human subjects are minimal and reasonable in relation to anticipated benefits of the research;
#Research involving the use of educational tests (cognitive, diagnostic, aptitude, achievement), surveys, interviews, or observations of public behavior that are not exempt under (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 personal identifiable information will be maintained throughout the research and thereafter.
# Selection of subjects is equitable given the purposes and the setting of the research;
#Research involving the collection or analysis of existing data, documents, records, pathological specimens, or diagnostic specimens, if such sources are a matter of public record 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.
# Researchers will seek Informed Consent appropriate to the research from each subject or the subject's legally authorized representative, and such consent will be appropriately documented (see Informed Consent Guidelines below);
#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 examine: (i) public benefit or service programs; (ii) procedures for obtaining benefits or services under such programs; (iii) possible changes in or alternatives to such programs or procedures; or (iv) possible changes in methods or levels of payment for benefits or services under such programs.
# The research plan makes appropriate provision for monitoring the data collected to ensure the safety of subjects;
#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.
# Appropriate provisions are made to protect the privacy of subjects and to maintain the confidentiality of data; and
# Where some or all of the subjects are likely to be vulnerable to coercion or undue influence, appropriate additional safeguards have been included to protect the rights and welfare of these subjects.
 
4.3.2 All proposals for research with human subjects will be processed by the IRB through an exemption letter, Expedited Review or Full Review. The IRB shall determine in its sole discretion which form of review is appropriate for each research protocol.
 
4.3.3  In reviewing research proposals, the IRB has the authority to approve as written, require modifications, defer review to a later date, disapprove or terminate any research involving human subjects conducted.
 
4.3.4  Research proposals approved by the IRB may be subject to further review by University officials as appropriate. However, those officials may not approve the research if it has not been approved by the IRB.
 
=== Levels of Review ===
 
==== Exempt Research and Limited Review ====
4.4.1.1 Certain categories of research protocols may be exempt from IRB review or may require limited IRB review. Research Protections staff, in consultation with the IRB Chair when necessary, shall make a determination regarding exemption or limited IRB review.
 
4.4.1.2  Research protocols involving the following will not be considered exempt from IRB review:
# Prisoners as a specifically recruited population;
# Children when the exemption category prohibits children as subjects;
# Research which requires oversight by other federal regulations (e.g., HIPAA, FDA) where exemption is not permitted;
# Research techniques which expose human subjects to more than minimal risk; or
# The deception of the human subject without prospective agreement by the subject.


==== Expedited Review ====
==== Expedited Review ====
a. Federal regulations permit an expedited review procedure for protocols that meet certain eligibility requirements. Such reviews may be carried out by the Chair of the IRB or by one or more experienced reviewers from among the members of the Board. In performing expedited reviews reviewers may exercise all of the authorities of the Board with the exception of disapproval. A research project may be disapproved only after full Board review as described in the next section. The Board shall be informed of all expedited reviews at its next full meeting.
4.4.2.1  Federal regulations permit an expedited review procedure for research protocols that meet certain eligibility requirements. Such reviews may be carried out by the Chair of the IRB or by one or more experienced reviewers from among the members of the Board. In performing expedited reviews, reviewers may exercise all of the authorities of the IRB with the exception of disapproval. A research project may be disapproved only after a Full Review by the IRB. The IRB shall be informed of all expedited reviews at its next full meeting.


b. Research activities that present no more than minimal risk (see glossary) to human subjects, and involve only procedures listed in one or more of the following categories, may be reviewed by the IRB through the expedited review procedure. The activities detailed below should not be deemed to be of minimal risk simply because they are included on this list. Inclusion merely means that the activity is eligible for review through the expedited review procedure when the specific circumstances of the proposed research involve no more than minimal risk to human subjects.
4.4.2.2  Classified research involving human subjects cannot be subject to an Expedited Review.


c. The expedited review procedure may not be used where identification of the subjects and/or their responses would reasonably place them at risk of criminal or civil liability or be damaging to the subjects' financial standing, employability, insurability, or reputation, or be stigmatizing, unless reasonable and appropriate protections will be implemented so that risks related to invasion of privacy and breach of confidentiality are no greater than minimal.
==== Full IRB Review ====
Full IRB Review must take place for all protocols that do not qualify for an Exempt or Expedited Review or as otherwise specified by the IRB.


d. The expedited review procedure may not be used for classified research involving human subjects. The standard requirements for informed consent (or its waiver, alteration, or exception) apply regardless of the type of review used by the IRB — expedited or full. The categories in this list apply regardless of the age of subjects, except as noted. Categories one 1-7 pertain to both initial and continuing IRB review.
=== Full IRB Reviews ===
4.5.1 The IRB shall engage in initial and continuing reviews of research protocols at their scheduled meetings. In order to conduct business, a majority of the members must be present, including at least one member who represents the nonscientific community. This constitutes a quorum.


=== Expedited Categories ===
4.5.2  Members may participate and be counted toward quorum in meetings via teleconferencing technology.
==== ====
#Clinical studies of drugs and medical devices only when condition (a) or (b) is met.
##Research on drugs for which an investigational new drug application (21 CFR Part 312) is not required. (Note: Research on marketed drugs that significantly increases the risks or decreases the acceptability of the risks associated with the use of the product is not eligible for expedited review.)
##Research on medical devices for which (i) an investigational device exemption application (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.
#Collection of blood samples by finger stick, heel stick, ear stick, or venipuncture as follows:
##From healthy, non-pregnant adults who weigh at least 110 pounds. For these subjects, the amounts drawn may not exceed 550 ml in an 8 week period and collection may not occur more frequently than 2 times per week; or
##From other adults and children, taking into consideration the age, weight, and health of the subjects, the collection procedure, the amount of blood to be collected, and the frequency with which it will be collected. For these subjects, the amount drawn may not exceed 5 ml, or 3 ml per kg, whichever is less, in an 8-week period, and collection may not occur more frequently than 2 times per week.
#Collection of data through noninvasive procedures, i.e., not involving general anesthesia or sedation, routinely employed in clinical practice, excluding procedures involving x-rays or microwaves. Where medical devices are employed, they must be cleared/approved for marketing. (Studies intended to evaluate the safety and effectiveness of the medical device are not generally eligible for expedited review, nor are studies of approved medical devices being considered for new indications.)
#Prospective collection of biological specimens for research purposes by noninvasive means.
#Research involving materials (data, documents, records, or specimens) that have been collected, or will be collected solely for non-research purposes (such as medical treatment or diagnosis).
#Collection of data from voice, video, digital, or image recordings made for research purposes.
#Research on individual or group characteristics or behavior (including, but not limited to, research on perception, cognition, motivation, identity, language, communication, cultural beliefs or practices, and social behavior) or research employing survey, interview, oral history, focus group, program evaluation, human factors evaluation, or quality assurance methodologies.
#Continuing review of research previously approved by the full IRB as follows:
##When (i) the research is permanently closed to the enrollment of new subjects; (ii) all subjects have completed all research-related interventions; and (iii) the research remains active only for long-term follow-up of subjects.
##When no subjects have been enrolled and no additional risks have been identified.
##When the remaining research activities are limited to data analysis.
#Continuing review of research, not conducted under an investigational new drug application or investigational device exemption where categories two (2) through eight (8) do not apply but the IRB has determined and documented at a convened meeting that the research involves no greater than minimal risk and no additional risks have been identified.


==== Full Board Review ====
4.5.3  Approval of research protocols shall be via a majority vote of the quorum. Should a quorum be lost during a meeting, the IRB may not take further action or vote until the quorum is restored.
Full board review must take place for all protocols that do not qualify as “exempt” or “expedited”, or as otherwise specified by the Board.


=== Procedures to Initiate Review ===
4.5.4  Minutes of each IRB meeting shall document the deliberations, actions, and votes for each research protocol whether undergoing initial or continuing review. IRB Chair shall record votes as the number of “For,” “Opposed,” and/or “Abstaining.” Minutes shall include notation and explanation of any unusual degree of risk or an approval period less than one year for any research protocol.


4.5.1 Prior to the execution of any research involving human subjects, investigators shall have completed the mandated education described at the beginning of this document, and they shall have completed and submitted to the IRB Administrator copies of the protocol form along with copies of the proposed informed consent statement. The protocol form must provide the following information:
4.5.5  IRB shall retain all records of its meetings and research protocols for at least three years after completion of the research or in accordance with the UNC System Record Retention Policy, whichever is longer.
#Name(s) and department(s) of investigator(s)
#Title of the study
#Signature of responsible faculty member
#Whether or not external funding is proposed
#Purpose of the study
#Description of subjects
#Description of methodology, including a copy of any instruments used
#Potential benefits and risks to the subject
#Anticipated beneficial knowledge resulting from the study
#Qualifications of investigator(s), e.g. a CV or experience in the specific research area
#Description of any deception
#Procedures for protecting the anonymity/confidentiality of subjects
#A copy of any recruiting materials or scripts.
#Method for insuring informed consent, including a copy of the proposed informed consent statement.


=== Informed Consent Guidelines ===
=== Informed Consent ===
4.6.1 Informed consent constitutes the very essence of protecting the rights of subjects. Obtaining the informed consent of a potential human subject (or the subject’s legally authorized representative) for participation in non-exempt research is a federally mandated safeguard to ensure the protection of the rights and welfare of all individual subjects. The IRB will carefully review the proposed method for obtaining informed consent and the content of the document prepared for participants’ signatures. For research that is not exempt from IRB review, the informed consent form must include the following information:
==== Informed Consent ====
#The title of the study, information on the purpose(s) of the research, a description of the method(s) and procedure(s) to be followed, including the intention to publish or disseminate the results of the study, and the amount of time the subject will spend in actual project participation.
Obtaining the Informed Consent of a potential human subject (or the subject’s legally authorized
#A description of any reasonably foreseeable risks or discomforts to the subject, including expected total time of participation. If disguised or deceptive procedures are to be used, a plan to debrief participants must be explained to the IRB.
representative) for participation in non-exempt research is a federally mandated safeguard to ensure the
#A description of any benefits to the subject or to others as a result of the information obtained from the research.
protection of the rights and welfare of all human subjects.
#A disclosure of appropriate alternative procedures that may be advantageous to the subject when making an informed decision whether or not to participate in the research (this pertains primarily to medical research and drug trials).
#A description of the measures to be taken to insure the confidentiality of data and the anonymity of individual subjects, if applicable, as well as any circumstances under which confidentiality CANNOT be guaranteed.
#The name and phone number of a contact person(s) who will be available to answer any questions the subject or his/her legally authorized representative may have regarding the research (student investigators must include the name, address, and phone number of his/her faculty supervisor), and "Questions regarding the protection of human subjects may be addressed to the IRB Administrator, Research and Sponsored Programs, Appalachian State University, Boone, NC 28608, (828) 262-2130, [email protected].”
#A clear explanation that participation is voluntary and that no penalty or loss of benefits to which the subject is otherwise entitled will occur should the subject either refuse to participate or decide to discontinue participation (at any time).
#Disclosure of costs to the subject, if any, because of his/her participation in the research; disclosure of compensation/reward to the subject, if any, for his/her participation in the research.
#For projects of more than minimal risk to subjects, a statement must be included that describes how the costs of medical care or other therapies required as a result of injury or mishap incurred while participating in the research will be handled. The Consent Form should also include information about the availability and extent of on-site medical treatment should an injury occur.
#The approval and expiration date for the consent form once approval of the project has been granted.
#The consent form must not include a statement releasing the investigator, sponsor, institution or its agents from liability or negligence.


4.6.2 These requirements are not intended to preempt applicable federal, state, or local laws which require additional information to be disclosed in order to be legally effective. The consent form shall document that the subject understands the information contained therein, and has had an opportunity to have any of his/her questions answered.
==== Complex Informed Consent ====
For complex Informed Consent forms, the investigator must provide a concise statement of the possible
risks and other key information regarding the research protocol to assist a prospective human subject or
their legally authorized representative to make an informed determination to participate or not in the
research.


4.6.3 The 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, or waives requirements to obtain informed consent provided that the IRB finds and documents:
==== Content of Consent Forms ====
#The research involves no more than minimal risk to the subjects;
For research that is not exempt from IRB review, Informed Consent forms shall include at a minimum the
#The waiver or alteration will not adversely affect the rights and welfare of the subjects;
following information:
#The research could not practicably be carried out without the waiver or alteration; and
#Whenever appropriate, the subjects will be provided with additional pertinent information after participation.


4.6.4 When a consent form requires the signatures of research subjects and/or their parents or legal guardians, a copy of the signed form must be given to the subject/parent/guardian and a copy must be retained by the researcher for a minimum of three years after completion of the project. The IRB may waive the requirement for the investigator to obtain a signed consent form for some or all subjects as described in 45 CFR Part 46.117.
# 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 that are experimental;
# A description of any reasonably foreseeable risks or discomforts to the subject;
# A description of any benefits to the subject or to others that may reasonably be expected from the research; and
# A disclosure of appropriate alternative procedures or courses of treatment, if any, that might be advantageous to the subject;
# A statement describing the extent, if any, to which confidentiality of records identifying the subject will be maintained;
# For research involving more than minimal risk, an explanation as to whether any compensation and an explanation as to whether any medical treatments are available if injury occurs and, if so, what they consist of, or where further information may be obtained;
# An explanation of whom to contact for answers to pertinent questions about the research and research subjects’ rights, and whom to contact in the event of a research-related injury to the subject;
# A statement that participation is voluntary, refusal to participate will involve no penalty or loss of benefits to which the subject is otherwise entitled, and the subject may discontinue participation at any time without penalty or loss of benefits to which the subject is otherwise entitled; and
# One of the following statements about any research that involves the collection of identifiable private information or identifiable bio-specimens:
## A statement that identifiers might be removed from the identifiable private information or identifiable bio-specimens and that, after such removal, the information or bio-specimens could be used for future research studies or distributed to another investigator for future research studies without additional informed consent from the subject or the legally authorized representative; or
## A statement that the subject’s information or bio-specimens collected as part of the research, even if identifiers are removed, will not be used or distributed for future research studies.


4.6.5 For exempt research, the researcher is expected to provide information to prospective subjects about the research. This information should include:
==== Federal, State and Local Law Requirements ====
#A statement of the purpose of the research
Informed Consents shall also conform to all requirements of applicable federal, state, or local laws which require information to be disclosed in order to be legally effective. The consent form shall document that the subject understands the information contained therein, and has had an opportunity to have any of their questions answered prior to, during and after participation in the research.
#An explanation of the procedures of the study
#Details of any foreseeable risks, benefits and compensation
#A clear explanation that participation is voluntary and that no penalty or loss of benefits to which the subject is otherwise entitled will occur should the subject either refuse to participate or decide to discontinue participation (at any time).
#Contact information for the investigator and faculty advisor if the investigator is a student.


4.6.6 In some cases, it may not be practical to provide this information to prospective subjects. In these cases of exempt research, investigators should provide an explanation of why it is impractical to provide this information to potential subjects to the IRB Administrators.
==== Alternation(s) of Informed Consent ====
The 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, or waives requirements to obtain Informed Consent if the IRB determines the following:
# The research involves no more than minimal risk to the subjects;
# The waiver or alteration will not adversely affect the rights and welfare of the human subjects;
# The research could not practicably be carried out without the waiver or alteration; and
# Whenever appropriate, the researcher will provide the human subjects with additional pertinent information after participation.


=== Investigator's Right of Appeal ===
==== Signed Consent Form(s) ====
When an Informed Consent form requires the signatures of research subjects and/or their parents or legally authorized representative (LAR), a copy of the signed form must be given to the subject/parent/LAR and a copy must be retained by the Principal Investigator for a minimum of three years after completion of the project.


4.7.1 It is the policy of Appalachian State University that the final decision regarding approval or disapproval of all protocols rests with the IRB. In accordance with federal regulations, no research involving human subjects may be conducted under Appalachian State University's auspices without the prior and continuing approval of the Board. Any investigator who disagrees with a decision of the Board may request a hearing before the duly-convened IRB to appeal its decision. Relevant arguments and/or witnesses may be presented on behalf of the investigator. The investigator may also request that the Authorized Institutional Official be informed of the appeal. However, final decision rests with the Board.
==== Waiver to Obtain Signed Consent Form ====
The IRB may waive the requirement for the Principal Investigator to obtain a signed consent form for some or all subjects if the IRB determines the following:


=== Continuing Review of Research ===
# That the only record linking the human subject and the research would be the Informed Consent form and the principal risk would be potential harm resulting from a breach of confidentiality. Each subject (or legally authorized representative) will be asked whether the human subject wants documentation linking the human subject with the research, and the subject's wishes will govern;
==== After a research protocol has been reviewed by the IRB, it is the investigator's responsibility to report to the Board any proposed changes in the research as well as any unanticipated problems that arise involving risk to subjects. If deemed necessary, the IRB Administrator may determine that reconsideration of the protocol by the full Board is warranted. If such a determination is made, the procedures governing initial review of protocols will be utilized. ====
# That the research presents no more than minimal risk of harm to human subjects and involves no procedures for which written consent is normally required outside of the research context; or
# If the human subjects or legally authorized representatives are members of a distinct cultural group or community in which signing forms is not the norm, that the research presents no more than minimal risk of harm to human subjects and provided there is an appropriate alternative mechanism for documenting that informed consent was obtained.


==== In addition, federal regulations require that the Board conduct continuing review of approved expedited and full Board approved proposals at least once per year. Exempted protocols require no continuing review. It is the principal investigator’s responsibility to initiate the request for continuation, which must include a summary of the protocol and a status report on the progress to date. In summary, the following must be submitted: ====
==== Written Statement ====
#The number of subjects accrued.
In cases in which the Informed Consent requirement is waived, the IRB may require the investigator to provide subjects or legally authorized representatives with a written statement regarding the research.
#A summary of any adverse events or unanticipated problems involving risk to subjects, and of any withdrawal of subjects or complaints about the research since the last review.
#A summary of findings, and any amendments or modifications to the study.
#A copy of the current informed consent document


==== '''Failure by the investigator to initiate this annual review prior to the expiration date of the approval shall result in immediate termination of the research.''' ====
=== Continuing Review and Post-Approval Monitoring ===
4.7.1  Continuing review will generally not be requested for minimal risk research unless the IRB documents the justification for continuing review within local practices or regulatory requirements.


==== Certain protocols may be reviewed more often than yearly, e.g.: ====
4.7.2  If continuing review is required, IRB approval may be for a maximum one-year period. The Principal Investigator (“PI”) is responsible for requesting continuing review prior to the expiration of the approval period. Failure of the PI to initiate this annual review prior to the expiration date of the approval may result in termination of the IRB approval.
#Where protocols are considered to involve high risk, or have a high risk/benefit ratio.
#Where studies are complex involving unusual levels or types of the risks.
#For projects conducted by investigators who previously failed to comply with the requirements of the IRB.
#For projects where information has come to the attention of the IRB that protocol changes have been made without IRB approval.


=== IRB Membership ===
4.7.3  The IRB may conduct for cause and not for cause post approval monitoring of approved IRB research protocols in the following situations:
# For cause monitoring may be the result of noncompliance, a reported incident, or other cause of concern identified by the IRB.
# Not for cause monitoring will be regular, ongoing and randomly selected from all active, non-exempt studies.
# Post approval monitoring may consist of record review, observing the consent process, or observing study procedures. One or more members of the IRB may participate in a monitoring event.


==== The Board shall consist of a minimum of five members, including: ====
=== Payments to Human Subjects ===
#One member whose primary concern is in a scientific area
4.8.1 The Office of Research Protections, in conjunction with the Contracts and Grants Accounting, is responsible for maintaining procedures related to human subject research and compensation.
#One member whose primary concern is in a nonscientific are
#One member who has no affiliation with Appalachian State University
#Additional members to insure ethical treatment of subjects
#IRB Administrator, ex officio


==== The regular members will be appointed by the Chancellor of the University for a term of three years and the Board will report to the Authorized Institutional Official. The Chancellor of the University shall designate the Chair of the IRB. ====
=== Noncompliance and Reportable Event ===
4.9.1 If at any time, the IRB becomes aware of unanticipated problems involving risks to human subjects, serious or continuing noncompliance with federal requirements, or terminations of the IRB, including ongoing human subject research which has not been reviewed by the IRB, the IRB shall request a meeting with the PI and suspend the research until the problem can be further evaluated.


=== IRB Meetings and Deadlines ===
4.9.2  In the event the IRB becomes aware of such noncompliance, the IO shall be notified of the situation immediately, and advised of any further sanctions subsequently recommended by the IRB.
==== Initial and continuing reviews of research will be conducted at meetings of the IRB convened monthly. In order to conduct business, a majority of the members must be present, including at least one member who represents the nonscientific community. This constitutes a quorum. Expedited reviews can be performed as described above in the absence of an IRB meeting. Teleconferencing may be used for any members to participate in the meeting, and they shall be counted toward the quorum. Approval of research is by a majority vote of the quorum. Should a quorum be lost during a meeting, the IRB may not take further action or vote until the quorum has been restored. ====


==== Review of proposed protocol changes will be conducted at IRB meetings with a quorum present, except where expedited review is appropriate. Minor changes in previously approved research can be approved under an expedited review procedure as above. Any revisions to a protocol should be incorporated into the written protocol with the revision dates noted on the protocol itself. ====
4.9.3  Possible sanctions the IRB may impose for noncompliance include, but are not limited to, suspending the Principal Investigator’s right to conduct or supervise research involving human subjects, taking possession of the data collected by the non-compliant PI, withholding or revoking academic credit to a student PI, and recommending discipline of a faculty or staff member to the Provost & Executive Vice Chancellor.


==== All necessary review materials must be submitted to the office of the IRB Administrator at least two weeks before the meeting at which they will be considered. Complete copies of all materials to be reviewed will be distributed to the full Board at least one week in advance of the meeting at which they will be considered. ====
4.9.4  Principal Investigators will receive notice of any such sanction within 3 business days of the determination by the IRB, and such sanction shall be final.


==== Minutes of each IRB meeting shall document the deliberations, actions, and votes for each protocol whether undergoing initial or continuing review. Votes shall be recorded as the number “For”, “Opposed”, and/or “Abstaining”. Any unusual degree of risk or an approval period less than one year shall be documented explicitly in the minutes. ====
4.9.5  As required by federal regulations, any decision of the IRB with respect to research involving human subjects is final. However, the convened IRB may review an investigator’s request for reconsideration to a determination regarding noncompliance and/or corrective actions as warranted by the presentation of new information or unusual circumstances. All investigator petitions must be made within 30 days of the investigator’s notification of the IRB’s sanction. The IRB will review an investigator’s request within 30 days, and the investigator will be notified in writing of the IRB’s decision within 14 days of the review.


==== There shall be a monthly summary of Board actions forwarded to the Dean of Graduate Studies. IRB records will be retained for at least three years, and records relating to research that is conducted will be retained for at least three years after completion of the research. ====
== Related University Policies ==
:[[Human Subject Research Recruitment|Appalachian State University’s Human Subject Research Recruitment Policy]]


== Additional References ==
== Additional References ==
 
:[https://www.govinfo.gov/content/pkg/USCODE-2011-title42/html/USCODE-2011-title42.htm Code of Federal Regulations, Title 42, Chapter 6(a) Public Health Service, Subchapter III Part H]
== Authority ==
:[https://www.hhs.gov/ohrp/regulations-and-policy/regulations/45-cfr-46/index.html Code of Federal Regulations, Title 45, Part 46 (Protection of Human Subjects)]
 
:[https://www.fda.gov/medical-devices/medical-device-databases/code-federal-regulations-title-21-food-and-drugs U.S. Food and Drug Administration Regulations, Title 21, Parts 50, 56, 312, 812]
:[https://www.ncleg.net/enactedlegislation/statutes/html/bychapter/chapter_90.html North Carolina Statute on Practice of Medicine]
:[https://researchprotections.appstate.edu/human-subjects Appalachian State University's Federal-wide Assurance]
:[https://researchprotections.appstate.edu/human-subjects-irb/irb-policies-and-guidelines Appalachian State University's Standard Operating Procedures for Human Subjects Research]


== Contact Information ==
== Contact Information ==
 
:Vice Provost for Research, (828) 262-7459, [email protected], [https://research.appstate.edu/ Office of Research]


== Original Effective Date ==
== Original Effective Date ==
:May 18, 2010


== Revision Dates ==
== Revision Dates ==
Approved 5/18/2010
:April 29, 2019
:December 1, 2021
:March 8, 2024


[[Category:Contents]]
[[Category:Contents]]
[[Category:Academic Affairs]]
[[Category:Academic Affairs]]

Latest revision as of 19:31, 8 March 2024

Policy 209

Purpose

This policy provides authority to the Institutional Review Board (hereinafter “IRB”) to provide ethical and regulatory oversight for research involving human subjects conducted by Appalachian State University, its faculty, staff, students and visitors.

Scope

This policy applies to all faculty, staff, students and any other individual engaged in research involving human subjects on the campus of the University, through funding provided by the University, on behalf of the University or in conjunction with University employees or students.

Definitions

Anonymity

Means that the identity of subjects cannot be matched to their responses either directly through identifiers or by "linked" or "coded" responses.

Confidentiality

Means not disclosing individually identifiable information received from a human subject to others in a manner inconsistent with the understanding of the original Informed Consent agreement.

Data Collection

Means any research procedure that is intended to elicit from or record the actions, reactions, attitudes, and/or behavioral manifestations of human subjects participating in a research project.

Exempt Research

Means human subject research activities which are minimal risk in nature and fall into one or more of the federally defined exempt research categories.

Expedited Review

Means a review by the IRB Chair or designee of research proposals which involve minimal risk or no-risk.

Full IRB Review

Means the review of proposals conducted during a convened IRB meeting at which a quorum has been established.

Human Subject

Means a living individual about whom a researcher (whether professional or student) conducting research that (i) Obtains information or biospecimens through intervention or interaction with the individual, and uses, studies, or analyzes the information or biospecimens; or (ii) Obtains, uses, studies, analyzes, or generates identifiable private information or identifiable bio-specimens.

Informed Consent

Means the voluntary agreement by an individual or an individual's legally authorized representative to participate in a particular study without any element of force, fraud, deceit, duress, or any other form of constraint or coercion. Valid consent requires voluntary action, competence, informed decision, and comprehension of terminology.

IRB

Means the University’s institutional review board.

Minimal Risk

Means that the probability and magnitude of harm(s) or discomfort(s) anticipated in the research are not greater than those ordinarily encountered in daily life or during the performance of routine physical or psychological examinations.

Research

Means a systematic investigation, including research development, testing, and evaluation, designed to develop or contribute to generalizable knowledge. Activities that meet this definition constitute research for purposes of this policy, whether or not they are conducted or supported under a program that is considered research for other purposes. For example, some demonstration and service programs may include research activities.

University

Means Appalachian State University

Vulnerable Populations

Means human subjects that are children, prisoners, pregnant persons, or any population that may be relatively or absolutely incapable of protecting their interests through the informed consent process.

Policy and Procedure Statements

Roles and Responsibilities

Protection of Research Subjects

The primary responsibility for the responsible conduct of research shall reside with the investigators who are conducting the research. However, other persons not involved directly share in the responsibility to establish and maintain an atmosphere where respect for the rights of individuals and compliance with applicable regulations is the standard.

Vice Provost for Research

The Chancellor has designated the University’s Vice Provost for Research ("VPR") as the authorized Institutional Officer ("IO") with responsibility for the University’s program for the protection of human subjects.

Members of IRB

4.1.3.1 The IRB shall report to the IO and consist of a minimum of five members, including:

  1. One member from a scientific area; and
  2. One member from a nonscientific area; and
  3. One member unaffiliated with the University; and
  4. Other additional members to provide expertise in research areas commonly employing human subjects, or expertise with unique or vulnerable populations to ensure ethical treatment of subjects; and
  5. The IRB Administrator, as an ex officio non-voting member.

4.1.3.2 The Chancellor shall appoint all members of the IRB for a term of one to three years and shall designate a Chair.

Office of Research Protections

The Office of Research Protections provides administrative support and leadership to the IRB, and is responsible for the interpretation and implementation of this policy, as well as addressing non-compliance with this policy. The Office of Research Protection is responsible for:

  1. Developing procedures to facilitate the review of human subjects research and to maintain compliance with federal regulations related to the protection of human subjects,
  2. Developing procedures and guidelines for the IRB and University community related to the protection of human subjects under this policy,
  3. Providing federal and state regulatory updates to the IRB and University Community, and
  4. Acting as liaison with federal regulators when necessary.

IRB Oversight

4.2.1 Any research involving human subjects, including internally funded, externally funded or unfunded research that involves University faculty, staff or students or is supported by or conducted on the University campus, must be reviewed and approved by the IRB prior to soliciting human subject participants or collecting any data from any human subject.

4.2.2 The IO has the authority to rely on another institution’s IRB approval for collaborative activities where human subject protections are the responsibility of the collaborating intuition’s human subjects program.

Review Requirements

4.3.1 The IRB shall only approve research protocols that satisfy all of the following requirements:

  1. Any risk(s) to human subjects are minimal and reasonable in relation to anticipated benefits of the research;
  2. Selection of subjects is equitable given the purposes and the setting of the research;
  3. Researchers will seek Informed Consent appropriate to the research from each subject or the subject's legally authorized representative, and such consent will be appropriately documented (see Informed Consent Guidelines below);
  4. The research plan makes appropriate provision for monitoring the data collected to ensure the safety of subjects;
  5. Appropriate provisions are made to protect the privacy of subjects and to maintain the confidentiality of data; and
  6. Where some or all of the subjects are likely to be vulnerable to coercion or undue influence, appropriate additional safeguards have been included to protect the rights and welfare of these subjects.

4.3.2 All proposals for research with human subjects will be processed by the IRB through an exemption letter, Expedited Review or Full Review. The IRB shall determine in its sole discretion which form of review is appropriate for each research protocol.

4.3.3 In reviewing research proposals, the IRB has the authority to approve as written, require modifications, defer review to a later date, disapprove or terminate any research involving human subjects conducted.

4.3.4 Research proposals approved by the IRB may be subject to further review by University officials as appropriate. However, those officials may not approve the research if it has not been approved by the IRB.

Levels of Review

Exempt Research and Limited Review

4.4.1.1 Certain categories of research protocols may be exempt from IRB review or may require limited IRB review. Research Protections staff, in consultation with the IRB Chair when necessary, shall make a determination regarding exemption or limited IRB review.

4.4.1.2 Research protocols involving the following will not be considered exempt from IRB review:

  1. Prisoners as a specifically recruited population;
  2. Children when the exemption category prohibits children as subjects;
  3. Research which requires oversight by other federal regulations (e.g., HIPAA, FDA) where exemption is not permitted;
  4. Research techniques which expose human subjects to more than minimal risk; or
  5. The deception of the human subject without prospective agreement by the subject.

Expedited Review

4.4.2.1 Federal regulations permit an expedited review procedure for research protocols that meet certain eligibility requirements. Such reviews may be carried out by the Chair of the IRB or by one or more experienced reviewers from among the members of the Board. In performing expedited reviews, reviewers may exercise all of the authorities of the IRB with the exception of disapproval. A research project may be disapproved only after a Full Review by the IRB. The IRB shall be informed of all expedited reviews at its next full meeting.

4.4.2.2 Classified research involving human subjects cannot be subject to an Expedited Review.

Full IRB Review

Full IRB Review must take place for all protocols that do not qualify for an Exempt or Expedited Review or as otherwise specified by the IRB.

Full IRB Reviews

4.5.1 The IRB shall engage in initial and continuing reviews of research protocols at their scheduled meetings. In order to conduct business, a majority of the members must be present, including at least one member who represents the nonscientific community. This constitutes a quorum.

4.5.2 Members may participate and be counted toward quorum in meetings via teleconferencing technology.

4.5.3 Approval of research protocols shall be via a majority vote of the quorum. Should a quorum be lost during a meeting, the IRB may not take further action or vote until the quorum is restored.

4.5.4 Minutes of each IRB meeting shall document the deliberations, actions, and votes for each research protocol whether undergoing initial or continuing review. IRB Chair shall record votes as the number of “For,” “Opposed,” and/or “Abstaining.” Minutes shall include notation and explanation of any unusual degree of risk or an approval period less than one year for any research protocol.

4.5.5 IRB shall retain all records of its meetings and research protocols for at least three years after completion of the research or in accordance with the UNC System Record Retention Policy, whichever is longer.

Informed Consent

Informed Consent

Obtaining the Informed Consent of a potential human subject (or the subject’s legally authorized representative) for participation in non-exempt research is a federally mandated safeguard to ensure the protection of the rights and welfare of all human subjects.

Complex Informed Consent

For complex Informed Consent forms, the investigator must provide a concise statement of the possible risks and other key information regarding the research protocol to assist a prospective human subject or their legally authorized representative to make an informed determination to participate or not in the research.

Content of Consent Forms

For research that is not exempt from IRB review, Informed Consent forms shall include at a minimum the following information:

  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 that are experimental;
  2. A description of any reasonably foreseeable risks or discomforts to the subject;
  3. A description of any benefits to the subject or to others that may reasonably be expected from the research; and
  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 medical treatments are available if injury occurs and, if so, what they consist of, or where further information may be obtained;
  7. An explanation of whom to contact for answers to pertinent questions about the research and research subjects’ rights, and whom to contact in the event of a research-related injury to the subject;
  8. A statement that participation is voluntary, refusal to participate will involve no penalty or loss of benefits to which the subject is otherwise entitled, and the subject may discontinue participation at any time without penalty or loss of benefits to which the subject is otherwise entitled; and
  9. One of the following statements about any research that involves the collection of identifiable private information or identifiable bio-specimens:
    1. A statement that identifiers might be removed from the identifiable private information or identifiable bio-specimens and that, after such removal, the information or bio-specimens could be used for future research studies or distributed to another investigator for future research studies without additional informed consent from the subject or the legally authorized representative; or
    2. A statement that the subject’s information or bio-specimens collected as part of the research, even if identifiers are removed, will not be used or distributed for future research studies.

Federal, State and Local Law Requirements

Informed Consents shall also conform to all requirements of applicable federal, state, or local laws which require information to be disclosed in order to be legally effective. The consent form shall document that the subject understands the information contained therein, and has had an opportunity to have any of their questions answered prior to, during and after participation in the research.

Alternation(s) of Informed Consent

The 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, or waives requirements to obtain Informed Consent if the IRB determines the following:

  1. The research involves no more than minimal risk to the subjects;
  2. The waiver or alteration will not adversely affect the rights and welfare of the human subjects;
  3. The research could not practicably be carried out without the waiver or alteration; and
  4. Whenever appropriate, the researcher will provide the human subjects with additional pertinent information after participation.

Signed Consent Form(s)

When an Informed Consent form requires the signatures of research subjects and/or their parents or legally authorized representative (LAR), a copy of the signed form must be given to the subject/parent/LAR and a copy must be retained by the Principal Investigator for a minimum of three years after completion of the project.

Waiver to Obtain Signed Consent Form

The IRB may waive the requirement for the Principal Investigator to obtain a signed consent form for some or all subjects if the IRB determines the following:

  1. That the only record linking the human subject and the research would be the Informed Consent form and the principal risk would be potential harm resulting from a breach of confidentiality. Each subject (or legally authorized representative) will be asked whether the human subject wants documentation linking the human subject with the research, and the subject's wishes will govern;
  2. That the research presents no more than minimal risk of harm to human subjects and involves no procedures for which written consent is normally required outside of the research context; or
  3. If the human subjects or legally authorized representatives are members of a distinct cultural group or community in which signing forms is not the norm, that the research presents no more than minimal risk of harm to human subjects and provided there is an appropriate alternative mechanism for documenting that informed consent was obtained.

Written Statement

In cases in which the Informed Consent requirement is waived, the IRB may require the investigator to provide subjects or legally authorized representatives with a written statement regarding the research.

Continuing Review and Post-Approval Monitoring

4.7.1 Continuing review will generally not be requested for minimal risk research unless the IRB documents the justification for continuing review within local practices or regulatory requirements.

4.7.2 If continuing review is required, IRB approval may be for a maximum one-year period. The Principal Investigator (“PI”) is responsible for requesting continuing review prior to the expiration of the approval period. Failure of the PI to initiate this annual review prior to the expiration date of the approval may result in termination of the IRB approval.

4.7.3 The IRB may conduct for cause and not for cause post approval monitoring of approved IRB research protocols in the following situations:

  1. For cause monitoring may be the result of noncompliance, a reported incident, or other cause of concern identified by the IRB.
  2. Not for cause monitoring will be regular, ongoing and randomly selected from all active, non-exempt studies.
  3. Post approval monitoring may consist of record review, observing the consent process, or observing study procedures. One or more members of the IRB may participate in a monitoring event.

Payments to Human Subjects

4.8.1 The Office of Research Protections, in conjunction with the Contracts and Grants Accounting, is responsible for maintaining procedures related to human subject research and compensation.

Noncompliance and Reportable Event

4.9.1 If at any time, the IRB becomes aware of unanticipated problems involving risks to human subjects, serious or continuing noncompliance with federal requirements, or terminations of the IRB, including ongoing human subject research which has not been reviewed by the IRB, the IRB shall request a meeting with the PI and suspend the research until the problem can be further evaluated.

4.9.2 In the event the IRB becomes aware of such noncompliance, the IO shall be notified of the situation immediately, and advised of any further sanctions subsequently recommended by the IRB.

4.9.3 Possible sanctions the IRB may impose for noncompliance include, but are not limited to, suspending the Principal Investigator’s right to conduct or supervise research involving human subjects, taking possession of the data collected by the non-compliant PI, withholding or revoking academic credit to a student PI, and recommending discipline of a faculty or staff member to the Provost & Executive Vice Chancellor.

4.9.4 Principal Investigators will receive notice of any such sanction within 3 business days of the determination by the IRB, and such sanction shall be final.

4.9.5 As required by federal regulations, any decision of the IRB with respect to research involving human subjects is final. However, the convened IRB may review an investigator’s request for reconsideration to a determination regarding noncompliance and/or corrective actions as warranted by the presentation of new information or unusual circumstances. All investigator petitions must be made within 30 days of the investigator’s notification of the IRB’s sanction. The IRB will review an investigator’s request within 30 days, and the investigator will be notified in writing of the IRB’s decision within 14 days of the review.

Related University Policies

Appalachian State University’s Human Subject Research Recruitment Policy

Additional References

Code of Federal Regulations, Title 42, Chapter 6(a) Public Health Service, Subchapter III Part H
Code of Federal Regulations, Title 45, Part 46 (Protection of Human Subjects)
U.S. Food and Drug Administration Regulations, Title 21, Parts 50, 56, 312, 812
North Carolina Statute on Practice of Medicine
Appalachian State University's Federal-wide Assurance
Appalachian State University's Standard Operating Procedures for Human Subjects Research

Contact Information

Vice Provost for Research, (828) 262-7459, [email protected], Office of Research

Original Effective Date

May 18, 2010

Revision Dates

April 29, 2019
December 1, 2021
March 8, 2024
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