Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Research Study Complaint Form, 25591 [E6-6457]
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25591
Federal Register / Vol. 71, No. 83 / Monday, May 1, 2006 / Notices
Survey, OMB No. 0920–0214) and other
federally sponsored surveys. The QDRL
conducts cognitive interviews, focus
groups, mini field-pretests, and
experimental research in laboratory and
field settings, both for applied
questionnaire evaluation and more basic
research on response errors in surveys.
The most common questionnaire
evaluation method is the cognitive
interview. In a cognitive interview, a
questionnaire design specialist
interviews a volunteer participant. The
interviewer administers the draft survey
questions as written, but also probes the
participant in depth about
interpretations of questions, recall
processes used to answer them, and
adequacy of response categories to
express answers, while noting points of
confusion and errors in responding.
Interviews are generally conducted in
small rounds of 10–15 interviews;
ideally, the questionnaire is re-worked
between rounds and revisions are tested
iteratively until interviews yield
relatively few new insights. When
possible, cognitive interviews are
conducted in the survey’s intended
mode of administration. For example,
when testing telephone survey
questionnaires, participants often
respond to the questions via a telephone
in a laboratory room. Under this
condition, the participant answers
without face-to-face interaction. QDRL
staff watch for response difficulties from
an observation room, and then conduct
a face-to-face debriefing with in-depth
probes. Cognitive interviewing provides
useful data on questionnaire
performance at minimal cost and
respondent burden. Similar
methodology has been adopted by other
federal agencies, as well as by academic
and commercial survey organizations.
NCHS is requesting 3 years of OMB
Clearance for the project. There are no
costs to respondents other than their
time.
ESTIMATED ANNUALIZED BURDEN
Respondents
Number of
respondents
per year
Number of
responses/
respondent
Avg. burden
response
(in hours)
Total burden
hours
2007 test volunteers ................................................................................................
500
1
1.2
600
Dated: April 25, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E6–6501 Filed 4–28–06; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2003N–0273] (formerly 03N–
0273)
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Research Study Complaint Form
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
cchase on PROD1PC60 with NOTICES
17:38 Apr 28, 2006
Dated: April 24, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6–6457 Filed 4–28–06; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Research Study Complaint Form’’ has
been approved by the Office of
Management and Budget (OMB) under
the Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT:
Karen L. Nelson, Office of Management
Programs (HFA–250), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–1482.
SUPPLEMENTARY INFORMATION: In the
Federal Register of December 16, 2005
(70 FR 74817), the agency announced
that the proposed information collection
had been submitted to OMB for review
and clearance under 44 U.S.C. 3507. An
SUMMARY:
VerDate Aug<31>2005
agency may not conduct or sponsor, and
a person is not required to respond to,
a collection of information unless it
displays a currently valid OMB control
number. OMB has now approved the
information collection and has assigned
OMB control number 0910–0579. The
approval expires on March 31, 2009. A
copy of the supporting statement for this
information collection is available on
the Internet at https://www.fda.gov/
ohrms/dockets.
Jkt 208001
[Docket No. 2006N–0166]
Agency Emergency Processing Under
the Office of Management and Budget
Review; MedWatch—The Food and
Drug Administration Safety
Information and Adverse Event
Reporting Program; Proposal to
Survey MedWatch Partners
Organizations
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
Office of Management and Budget
(OMB) for emergency processing under
the Paperwork Reduction Act of 1995
(the PRA). This notice solicits
comments on a proposal for the
MedWatch program to deploy and
conduct a web-based customer
satisfaction survey of certain health care
professional trade and specialty
organizations that voluntarily have
chosen to participate in the FDA
MedWatch’s Partners program. The
survey will solicit information about the
utility of the FDA MedWatch safety
alerts and monthly safety labeling
changes that are posted on the
MedWatch Web site and disseminated
to partner organizations for sharing with
members of the organizations.
DATES: Fax written comments on the
collection of information by May 31,
2006. FDA is requesting approval of this
emergency processing by May 31, 2006.
ADDRESSES: OMB is still experiencing
significant delays in the regular mail,
including first class and express mail,
and messenger deliveries are not being
accepted. To ensure that comments on
the information collection are received,
OMB recommends that comments be
faxed to the Office of Information and
Regulatory Affairs, OMB, Attn: Fumie
Yokota, Desk Officer for FDA, Fax: 202–
395–6974.
FOR FURTHER INFORMATION CONTACT:
Karen Nelson, Office of Management
Programs (HFA–250), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–1482.
SUPPLEMENTARY INFORMATION: FDA has
requested emergency processing of this
E:\FR\FM\01MYN1.SGM
01MYN1
]]>Agencies
[Federal Register Volume 71, Number 83 (Monday, May 1, 2006)]
[Notices]
[Page 25591]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-6457]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 2003N-0273] (formerly 03N-0273)
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approval; Research Study Complaint Form
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that a
collection of information entitled ``Research Study Complaint Form''
has been approved by the Office of Management and Budget (OMB) under
the Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT: Karen L. Nelson, Office of Management
Programs (HFA-250), Food and Drug Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301-827-1482.
SUPPLEMENTARY INFORMATION: In the Federal Register of December 16, 2005
(70 FR 74817), the agency announced that the proposed information
collection had been submitted to OMB for review and clearance under 44
U.S.C. 3507. An agency may not conduct or sponsor, and a person is not
required to respond to, a collection of information unless it displays
a currently valid OMB control number. OMB has now approved the
information collection and has assigned OMB control number 0910-0579.
The approval expires on March 31, 2009. A copy of the supporting
statement for this information collection is available on the Internet
at https://www.fda.gov/ohrms/dockets.
Dated: April 24, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6-6457 Filed 4-28-06; 8:45 am]
BILLING CODE 4160-01-S
