In May 2015, the OMB approved a
quantitative questionnaire to capture current immunohistochemistry
validation practices of laboratories. The CAP and CDC respectfully
ask OMB to approve a revised version of the questionnaire that is
strictly focused on the qualitative aspect and which will allow for
a fuller exploration of the factors that underlie the adoption or
non-adoption reasons and rates of the immunohistochemistry
validation laboratory practice guideline by laboratorians. We are
submitting a revision request to OMB #0920-1067 for permission to
conduct a limited telephone interview and two in-person focus
groups, only for the immunohistochemistry validation laboratory
practice guideline.
US Code:
42
USC 241 Name of Law: Public Health and Welfare Act
This revision includes three
types of laboratory professionals who were not included in the
original OMB-approved submission: pathology chairs, laboratory
supervisors, and histotechnologists. Because the OMB-approved IHC
post-survey has been completed, this request for OMB approval of
additional data collection (telephone interviews and focus groups)
is a reduction of burden.
On behalf of this Federal agency, I certify that
the collection of information encompassed by this request complies
with 5 CFR 1320.9 and the related provisions of 5 CFR
1320.8(b)(3).
The following is a summary of the topics, regarding
the proposed collection of information, that the certification
covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a
benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control
number;
If you are unable to certify compliance with any of
these provisions, identify the item by leaving the box unchecked
and explain the reason in the Supporting Statement.