Pediatric Advisory Committee; Notice of Meeting, 78284 [2011-32205]
Download as PDF
78284
Federal Register / Vol. 76, No. 242 / Friday, December 16, 2011 / Notices
accommodated during the scheduled
open public hearing session, FDA may
conduct a lottery to determine the
speakers for the scheduled open public
hearing session. The contact person will
notify interested persons regarding their
request to speak by January 19, 2012.
Persons attending FDA’s advisory
committee meetings are advised that the
Agency is not responsible for providing
access to electrical outlets.
FDA welcomes the attendance of the
public at its advisory committee
meetings and will make every effort to
accommodate persons with physical
disabilities or special needs. If you
require special accommodations due to
a disability, please contact Philip
Bautista at least 7 days in advance of the
meeting.
FDA is committed to the orderly
conduct of its advisory committee
meetings. Please visit our Web site at
https://www.fda.gov/
AdvisoryCommittees/
AboutAdvisoryCommittees/ucm111462.
htm for procedures on public conduct
during advisory committee meetings.
Notice of this meeting is given under
the Federal Advisory Committee Act (5
U.S.C. app. 2).
Dated: December 6, 2011.
Jill Hartzler Warner,
Acting Associate Commissioner for Special
Medical Programs.
[FR Doc. 2011–32206 Filed 12–15–11; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2011–N–0002]
Pediatric Advisory Committee; Notice
of Meeting
AGENCY:
Food and Drug Administration,
HHS.
jlentini on DSK4TPTVN1PROD with NOTICES
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). The meeting will be open to the
public.
Name of Committee: Pediatric
Advisory Committee.
General Function of the Committee:
To provide advice and
recommendations to the Agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on Monday, January 30, 2012 from
8 a.m. to 4 p.m. and on Tuesday,
January 31, 2012 from 9 a.m. to 12 noon.
Location: Hilton Gaithersburg Hotel,
620 Perry Pkwy., Gaithersburg, MD
VerDate Mar<15>2010
16:42 Dec 15, 2011
Jkt 226001
20877. The hotel’s phone number is
(301) 977–8900.
Contact Person: Walter Ellenberg,
Office of Pediatric Therapeutics, Office
of the Commissioner, Food and Drug
Administration, Bldg. 32, Rm. 5154,
10903 New Hampshire Ave., Silver
Spring, MD 20993, (301) 796–8524,
email: Walter.Ellenberg@fda.hhs.gov, or
FDA Advisory Committee Information
Line, 1–(800) 741–8138 ((301) 443–0572
in the Washington, DC area), and follow
the prompts to the desired center or
product area. Please call the Information
Line for up-to-date information on this
meeting. A notice in the Federal
Register about last minute modifications
that impact a previously announced
advisory committee meeting cannot
always be published quickly enough to
provide timely notice. Therefore, you
should always check the Agency’s Web
site and call the appropriate advisory
committee hot line/phone line to learn
about possible modifications before
coming to the meeting.
Agenda: The Pediatric Advisory
Committee will meet to discuss
pediatric-focused safety reviews, as
mandated by the Best Pharmaceuticals
for Children Act and the Pediatric
Research Equity Act for Prevnar 13
(Pneumococcal 13-valent Conjugate
Vaccine (Diphtheria CRM197 Protein),
Cervarix (Human Papillomavirus
Bivalent (Types 16 and 18) vaccine,
recombinant, Focalin XR
(dexmethylphenidate), Daytrana
(methylphenidate), Seroquel
(quetiapine), Pancreaze (pancrelipase),
Zenpep (pancrelipase), Creon
(pancrelipase), Xerese cream 5%/1%
(acyclovir and hydrocortisone), Xolair
(omalizumab), Benicar (olmesartan
medoxomil), Atacand (candesartan
cilexetil), Mirena (levonorgestrel—
releasing intrauterine system), Plan B
One Step (levonorgestrel), and Flomax
(tamsulosin).
FDA intends to make background
material available to the public no later
than 2 business days before the meeting.
If FDA is unable to post the background
material on its Web site prior to the
meeting, the background material will
be made publicly available at the
location of the advisory committee
meeting, and the background material
will be posted on FDA’s Web site after
the meeting. Background material is
available at https://www.fda.gov/
AdvisoryCommittees/Calendar/
default.htm. Scroll down to the
appropriate advisory committee link.
Procedure: Interested persons may
present data, information, or views,
orally or in writing, on issues pending
before the committee. Written
submissions may be made to the contact
PO 00000
Frm 00060
Fmt 4703
Sfmt 4703
person on or before January 24, 2012.
Oral presentations from the public will
be scheduled between approximately
1 p.m. and 2 p.m. Those individuals
interested in making formal oral
presentations should notify the contact
person and submit a brief statement of
the general nature of the evidence or
arguments they wish to present, the
names and addresses of proposed
participants, and an indication of the
approximate time requested to make
their presentation on or before January
16, 2012. Time allotted for each
presentation may be limited. If the
number of registrants requesting to
speak is greater than can be reasonably
accommodated during the scheduled
open public hearing session, FDA may
conduct a lottery to determine the
speakers for the scheduled open public
hearing session. The contact person will
notify interested persons regarding their
request to speak by January 17, 2012.
Persons attending FDA’s advisory
committee meetings are advised that the
Agency is not responsible for providing
access to electrical outlets.
FDA welcomes the attendance of the
public at its advisory committee
meetings and will make every effort to
accommodate persons with physical
disabilities or special needs. If you
require special accommodations due to
a disability, please contact Walter
Ellenberg at least 7 days in advance of
the meeting.
FDA is committed to the orderly
conduct of its advisory committee
meetings. Please visit our Web site at
https://www.fda.gov/
AdvisoryCommittees/
AboutAdvisoryCommittees/
ucm111462.htm for procedures on
public conduct during advisory
committee meetings.
Notice of this meeting is given under
the Federal Advisory Committee Act (5
U.S.C. app. 2).
Dated: December 6, 2011.
Jill Hartzler Warner,
Acting Associate Commissioner for Special
Medical Programs.
[FR Doc. 2011–32205 Filed 12–15–11; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center For Scientific Review; Notice of
Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
E:\FR\FM\16DEN1.SGM
16DEN1
Agencies
[Federal Register Volume 76, Number 242 (Friday, December 16, 2011)]
[Notices]
[Page 78284]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-32205]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2011-N-0002]
Pediatric Advisory Committee; Notice of Meeting
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
This notice announces a forthcoming meeting of a public advisory
committee of the Food and Drug Administration (FDA). The meeting will
be open to the public.
Name of Committee: Pediatric Advisory Committee.
General Function of the Committee: To provide advice and
recommendations to the Agency on FDA's regulatory issues.
Date and Time: The meeting will be held on Monday, January 30, 2012
from 8 a.m. to 4 p.m. and on Tuesday, January 31, 2012 from 9 a.m. to
12 noon.
Location: Hilton Gaithersburg Hotel, 620 Perry Pkwy., Gaithersburg,
MD 20877. The hotel's phone number is (301) 977-8900.
Contact Person: Walter Ellenberg, Office of Pediatric Therapeutics,
Office of the Commissioner, Food and Drug Administration, Bldg. 32, Rm.
5154, 10903 New Hampshire Ave., Silver Spring, MD 20993, (301) 796-
8524, email: Walter.Ellenberg@fda.hhs.gov, or FDA Advisory Committee
Information Line, 1-(800) 741-8138 ((301) 443-0572 in the Washington,
DC area), and follow the prompts to the desired center or product area.
Please call the Information Line for up-to-date information on this
meeting. A notice in the Federal Register about last minute
modifications that impact a previously announced advisory committee
meeting cannot always be published quickly enough to provide timely
notice. Therefore, you should always check the Agency's Web site and
call the appropriate advisory committee hot line/phone line to learn
about possible modifications before coming to the meeting.
Agenda: The Pediatric Advisory Committee will meet to discuss
pediatric-focused safety reviews, as mandated by the Best
Pharmaceuticals for Children Act and the Pediatric Research Equity Act
for Prevnar 13 (Pneumococcal 13-valent Conjugate Vaccine (Diphtheria
CRM197 Protein), Cervarix (Human Papillomavirus Bivalent (Types 16 and
18) vaccine, recombinant, Focalin XR (dexmethylphenidate), Daytrana
(methylphenidate), Seroquel (quetiapine), Pancreaze (pancrelipase),
Zenpep (pancrelipase), Creon (pancrelipase), Xerese cream 5%/1%
(acyclovir and hydrocortisone), Xolair (omalizumab), Benicar
(olmesartan medoxomil), Atacand (candesartan cilexetil), Mirena
(levonorgestrel--releasing intrauterine system), Plan B One Step
(levonorgestrel), and Flomax (tamsulosin).
FDA intends to make background material available to the public no
later than 2 business days before the meeting. If FDA is unable to post
the background material on its Web site prior to the meeting, the
background material will be made publicly available at the location of
the advisory committee meeting, and the background material will be
posted on FDA's Web site after the meeting. Background material is
available at https://www.fda.gov/AdvisoryCommittees/Calendar/default.htm. Scroll down to the appropriate advisory committee link.
Procedure: Interested persons may present data, information, or
views, orally or in writing, on issues pending before the committee.
Written submissions may be made to the contact person on or before
January 24, 2012. Oral presentations from the public will be scheduled
between approximately 1 p.m. and 2 p.m. Those individuals interested in
making formal oral presentations should notify the contact person and
submit a brief statement of the general nature of the evidence or
arguments they wish to present, the names and addresses of proposed
participants, and an indication of the approximate time requested to
make their presentation on or before January 16, 2012. Time allotted
for each presentation may be limited. If the number of registrants
requesting to speak is greater than can be reasonably accommodated
during the scheduled open public hearing session, FDA may conduct a
lottery to determine the speakers for the scheduled open public hearing
session. The contact person will notify interested persons regarding
their request to speak by January 17, 2012.
Persons attending FDA's advisory committee meetings are advised
that the Agency is not responsible for providing access to electrical
outlets.
FDA welcomes the attendance of the public at its advisory committee
meetings and will make every effort to accommodate persons with
physical disabilities or special needs. If you require special
accommodations due to a disability, please contact Walter Ellenberg at
least 7 days in advance of the meeting.
FDA is committed to the orderly conduct of its advisory committee
meetings. Please visit our Web site at https://www.fda.gov/AdvisoryCommittees/AboutAdvisoryCommittees/ucm111462.htm for procedures
on public conduct during advisory committee meetings.
Notice of this meeting is given under the Federal Advisory
Committee Act (5 U.S.C. app. 2).
Dated: December 6, 2011.
Jill Hartzler Warner,
Acting Associate Commissioner for Special Medical Programs.
[FR Doc. 2011-32205 Filed 12-15-11; 8:45 am]
BILLING CODE 4160-01-P