Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; General Administrative Procedures: Citizen Petitions; Petition for Reconsideration or Stay of Action; Advisory Opinions, 60851 [2014-24051]
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Federal Register / Vol. 79, No. 195 / Wednesday, October 8, 2014 / Notices
Ryan (Caroline.Ryan@acl.hhs.gov) to
register. Registrants will receive
confirmation after they have been
accepted.
Webcast of the Public Workshop: This
public workshop will also be available
by webcast. Those interested in joining
the webcast must register no later than
October 14, 2014. Early registration is
recommended; conference lines are
limited. To register for the webcast,
please visit: https://
attendee.gotowebinar.com/register/
2329630204976253953. Call details will
be sent to all registered participants
after October 14, 2014.
Requests for Public Comment: This
public workshop will include topicfocused sessions with opportunities for
public comment in-person or via
webcast. The agencies will do their best
to accommodate requests to make public
comments. Individuals and
organizations with common interests are
urged to consolidate or coordinate their
comments.
Comments: The agencies seek broad
input from stakeholders and experts on
the use of health information technology
(health IT) for the purposes of
developing an integrated, personcentered plan, including how to
improve communication and
collaboration among community-based
organizations and health care partners.
To obtain broad public comment, the
Agencies are soliciting comments on all
aspects of the public workshop topics.
The deadline for submitting
comments related to this public
workshop is October 31, 2014.
Please submit comments to:
personcenteredhealthIT@hhs.gov
Transcript: The meeting will be
transcribed. A transcript and meeting
materials will be posted on the
healthit.gov Web site at: https://
healthitgov-stage.ahrqstg.org/personcentered-care.
Dated: October 1, 2014.
Jacob Reider,
Deputy National Coordinator for Health
Information Technology.
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60851
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Food and Drug Administration
[Docket No. FDA–2011–N–0627]
[Docket No. FDA–2010–N–0493]
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
General Administrative Procedures:
Citizen Petitions; Petition for
Reconsideration or Stay of Action;
Advisory Opinions
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Additional Criteria and Procedures for
Classifying Over-the-Counter Drugs as
Generally Recognized as Safe and
Effective and Not Misbranded
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
AGENCY:
Food and Drug Administration,
HHS.
Notice.
ACTION:
Notice.
SUMMARY:
The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘General Administrative Procedures:
Citizen Petitions; Petition for
Reconsideration or Stay of Action;
Advisory Opinions’’ has been approved
by the Office of Management and
Budget (OMB) under the Paperwork
Reduction Act of 1995.
SUMMARY:
FOR FURTHER INFORMATION CONTACT:
FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 8455
Colesville Rd., COLE–14526, Silver
Spring, MD 20993–0002, PRAStaff@
fda.hhs.gov.
FOR FURTHER INFORMATION CONTACT:
On June
12, 2014, the Agency submitted a
proposed collection of information
entitled ‘‘General Administrative
Procedures: Citizen Petitions; Petition
for Reconsideration or Stay of Action;
Advisory Opinions’’ 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 0910–0183. The
approval expires on August 31, 2017. A
copy of the supporting statement for this
information collection is available on
the Internet at https://www.reginfo.gov/
public/do/PRAMain.
SUPPLEMENTARY INFORMATION:
SUPPLEMENTARY INFORMATION:
Dated: October 2, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Additional Criteria and Procedures for
Classifying Over-the-Counter Drugs as
Generally Recognized as Safe and
Effective and Not Misbranded’’ has been
approved by the Office of Management
and Budget (OMB) under the Paperwork
Reduction Act of 1995.
FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 8455
Colesville Rd., COLE–14526, Silver
Spring, MD 20993–0002, PRAStaff@
fda.hhs.gov.
On June
25, 2014, the Agency submitted a
proposed collection of information
entitled ‘‘Additional Criteria and
Procedures for Classifying Over-theCounter Drugs as Generally Recognized
as Safe and Effective and Not
Misbranded’’ 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 0910–0688. The
approval expires on August 31, 2017. A
copy of the supporting statement for this
information collection is available on
the Internet at https://www.reginfo.gov/
public/do/PRAMain.
[FR Doc. 2014–24051 Filed 10–7–14; 8:45 am]
Dated: October 2, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
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Agencies
[Federal Register Volume 79, Number 195 (Wednesday, October 8, 2014)]
[Notices]
[Page 60851]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-24051]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2011-N-0627]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approval; General Administrative Procedures:
Citizen Petitions; Petition for Reconsideration or Stay of Action;
Advisory Opinions
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that a
collection of information entitled ``General Administrative Procedures:
Citizen Petitions; Petition for Reconsideration or Stay of Action;
Advisory Opinions'' has been approved by the Office of Management and
Budget (OMB) under the Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations,
Food and Drug Administration, 8455 Colesville Rd., COLE-14526, Silver
Spring, MD 20993-0002, PRAStaff@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: On June 12, 2014, the Agency submitted a
proposed collection of information entitled ``General Administrative
Procedures: Citizen Petitions; Petition for Reconsideration or Stay of
Action; Advisory Opinions'' 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 0910-0183.
The approval expires on August 31, 2017. A copy of the supporting
statement for this information collection is available on the Internet
at https://www.reginfo.gov/public/do/PRAMain.
Dated: October 2, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014-24051 Filed 10-7-14; 8:45 am]
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