Research activities in which the involvement of human
participants shall be limited to one or more of the following categories shall
be exempt from this chapter unless the research is covered by other sections of
this chapter. The HRRC shall determine whether the proposed research project
satisfies at least one of the following exemption categories in this section
before the research may be conducted pursuant to the exemption provided under
this section:
1. Category 1. Research
conducted in established or commonly accepted educational settings, involving
normal educational practices that are not likely to impact adversely student
opportunity to learn required educational content or the assessment of
educators who provide instruction, such as:
a.
Research on regular and special education instructional strategies;
or
b. Research on the effectiveness
of or the comparison among instructional techniques, curriculum, or classroom
management methods.
2.
Category 2. Research involving the use of educational tests (cognitive,
diagnostic, aptitude, or achievement), survey procedures, interview procedures,
or observation of public behavior (including visual or auditory recording),
unless:
a. Information obtained is recorded
in such a manner that human subjects can be identified, directly or through
identifiers linked to the subjects;
b. 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, educational advancement, or reputation; or
c. The information obtained is recorded in
such a manner that human subjects can be identified, directly or through
identifiers linked to the subjects and the HRRC conducts a limited review to
make the determination required by
22VAC30-40-70 J
7.
3. Category 3. Research involving benign
behavioral interventions.
a. Research
involving benign behavioral interventions in conjunction with the collection of
information from an adult subject through verbal or written responses,
including data entry, or audiovisual recording if the subject prospectively
agrees to the intervention and information collection and at least one of the
following criteria is met:
(1) The
information obtained is recorded by the investigator in such a manner that the
identity of the human subjects cannot readily be ascertained, directly or
through identifiers linked to the subjects;
(2) Any disclosure of the human subjects'
responses outside the research would not reasonably place the subjects at risk
of criminal or civil liability or be damaging to the subjects' financial
standing, employability, educational advancement, or reputation; or
(3) The information obtained is recorded by
the investigator in such a manner that the identity of the human subjects can
readily be ascertained, directly or through identifiers linked to the subjects,
and the HRRC conducts a limited review to make the determination required by
22VAC30-40-70 J
7.
b. For the purpose of this subsection, benign
behavioral interventions are brief in duration, harmless, painless, not
physically invasive, and not likely to have a significant adverse lasting
impact on the subjects, and the investigator has no reason to think the
subjects will find the interventions offensive or embarrassing. Provided all of
these criteria are met, examples of benign behavioral interventions include
having the subjects play an online game, having them solve puzzles under
various noise conditions, or having them decide how to allocate a nominal
amount of received cash between themselves and someone else.
c. If the research involves deceiving the
subjects regarding the nature or purposes of the research, this exemption is
not applicable unless a subject authorizes the deception through a prospective
agreement to participate in research in circumstances in which a subject is
informed that he will be unaware of or misled regarding the nature or purposes
of the research.
4.
Category 4. Secondary research for which consent is not required: Secondary
research using identifiable private information, if at least one of the
following criteria is met:
a. The research
involves the collection or study of existing data, documents, records,
pathological specimens, or diagnostic specimens, if these sources are publicly
available ;
b. The information is
recorded by the investigator in a manner that subjects (i) cannot be
identified, directly or through identifiers linked to the subjects; (ii) the
investigator does not contact the subjects; and (iii) the investigator will not
reidentify the subject;
c. The
research involves only information collection and analysis involving the
investigator's use of identifiable health information when that use is
regulated under 45 CFR Part
160, General Administrative Requirements, and Part
164, Security and Privacy, Subparts A and E, for the purposes of "health care
operations'' or "research'' as those terms are defined at
45
CFR
164.501 or for "public health activities
and purposes'' as described under
45
CFR
164.512(b); or
d. The research is conducted by, or on behalf
of, the department using department-generated or department-collected
information obtained for nonresearch activities if the research generates
identifiable private information that is or will be maintained on information
technology that is subject to and in compliance with § 208(b) of the
E-Government Act of 2002,
44 USC
§
3501 note; if all of the identifiable
private information collected, used, or generated as part of the activity will
be maintained in systems of records subject to the Privacy Act of 1974,
5 USC §
552a; and if applicable, the information used
in the research was collected subject to the Paperwork Reduction Act of 1995,
44 USC
§
3501 et seq.
5. Category 5. Research and demonstration
projects conducted by or subject to the approval of the commissioner, which are
designed to study, evaluate, or otherwise examine:
a. Public benefit or service
programs;
b. Procedures for
obtaining benefits or services under those programs;
c. Possible changes in or alternatives to
those programs or procedures; or
d.
Possible changes in methods or levels of payment for benefits or services under
those programs.
6.
Category 6. Taste and food quality evaluation and consumer acceptance studies:
a. If wholesome foods without additives are
consumed; or
b. 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.
7. Category 7. Storage or maintenance for
secondary research for which broad consent is required. Storage or maintenance
of identifiable private information for potential secondary research use if the
HRRC conducts a limited review and makes the determinations required by
22VAC30-40-70 J
8.
8. Category 8. Secondary research for which
broad consent is required: Research involving the use of identifiable private
information, if it meets the following criteria:
a. Broad consent for the storage,
maintenance, and secondary research use of the identifiable private information
is obtained in accordance with
22VAC30-40-100 A
and D;
b. Documentation of informed
consent or waiver of documentation of consent is obtained in accordance with
22VAC30-40-100 L;
c. The HRRC conducts a limited review and
makes the determination required by
22VAC30-40-70 J 7
and makes the determination that the research to be conducted is within the
scope of the broad consent referenced in subdivision 1 of this subsection;
and
d. The investigator does not
include returning individual research results to subjects as part of the study
plan. The investigator shall not be prevented from abiding by any legal
requirements to return individual research results.