The Food and Drug Administration Food Safety Modernization Act: Focus on Strategic Implementation of Prevention-Oriented Import Safety Programs; Public Meetings, 28035-28037 [2016-10799]
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Federal Register / Vol. 81, No. 89 / Monday, May 9, 2016 / Proposed Rules
(vi) The affected fuel pumps have a
combination of P/Ns 568–1–28300–001, 568–
1–28300–002, and 568–1–28300–101.
(2) For affected fuel pumps that have a part
number or combination of part numbers that
are specified in paragraphs (h)(2)(i) through
(h)(2)(iii) of this AD: Do the replacement
within 96 months after the effective date of
this AD.
(i) All of the affected fuel pumps have P/
N 568–1–28300–100.
(ii) All of the affected fuel pumps have P/
N 568–1–28300–101.
(iii) The affected fuel pumps have a
combination of P/Ns 568–1–28300–100 and
568–1–28300–101.
(i) Definitions
(1) For the purpose of this AD, an ‘‘affected
fuel pump’’ is defined as any pump having
P/N 568–1–28300–001, 568–1–28300–002,
568–1–28300–100, or 568–1–28300–101.
(2) For the purpose of this AD, a
‘‘serviceable fuel pump’’ is a pump having a
part number not listed in paragraph (i)(1) of
this AD.
(j) No Reporting Requirement
Although Airbus Service Bulletin A330–
28–3127, Revision 01, dated September 24,
2015; Airbus Service Bulletin A340–28–4138,
Revision 01, dated September 24, 2015; or
Airbus Service Bulletin A340–28–5060,
Revision 01, dated September 24, 2015,
specifies to submit certain information to the
manufacturer, and specifies that action as
‘‘RC’’ (Required for Compliance), this AD
does not include that requirement.
mstockstill on DSK3G9T082PROD with PROPOSALS
(k) Parts Installation Prohibition
After the identification of the fuel pump
part numbers as required by paragraph (g) of
this AD, comply with the prohibition
required by paragraph (k)(1) or (k)(2) of this
AD, as applicable.
(1) For an airplane that does not have an
affected fuel pump installed: After the
identification of the fuel pump part numbers
as required by paragraph (g) of this AD, do
not install an affected fuel pump.
(2) For an airplane that has an affected fuel
pump installed: After modification of an
airplane as required by paragraph (h) of this
AD, no person may install an affected fuel
pump on any airplane.
(l) Credit for Previous Actions
This paragraph provides credit for actions
required by paragraphs (g) and (h) of this AD,
if those actions were performed before the
effective date of this AD using service
information included in paragraphs (l)(1),
(l)(2), and (l)(3) of this AD, which are not
incorporated by reference in this AD.
(1) Airbus Service Bulletin A330–28–3127
dated July 14, 2015.
(2) Airbus Service Bulletin A340–28–4138
dated July 14, 2015.
(3) Airbus Service Bulletin A340–28–5060
dated July 14, 2015.
(m) Other FAA AD Provisions
The following provisions also apply to this
AD:
(1) Alternative Methods of Compliance
(AMOCs): The Manager, International
Branch, ANM–116, Transport Airplane
VerDate Sep<11>2014
16:16 May 06, 2016
Jkt 238001
Directorate, FAA, has the authority to
approve AMOCs for this AD, if requested
using the procedures found in 14 CFR 39.19.
In accordance with 14 CFR 39.19, send your
request to your principal inspector or local
Flight Standards District Office, as
appropriate. If sending information directly
to the International Branch, send it to ATTN:
Vladimir Ulyanov, Aerospace Engineer,
International Branch, ANM–116, Transport
Airplane Directorate, FAA, 1601 Lind
Avenue SW., Renton, WA 98057–3356;
telephone: 425–227–1138; fax: 425–227–
1149. Information may be emailed to: 9ANM-116-AMOC-REQUESTS@faa.gov.
Before using any approved AMOC, notify
your appropriate principal inspector, or
lacking a principal inspector, the manager of
the local flight standards district office/
certificate holding district office. The AMOC
approval letter must specifically reference
this AD.
(2) Contacting the Manufacturer: For any
requirement in this AD to obtain corrective
actions from a manufacturer, the action must
be accomplished using a method approved
by the Manager, International Branch, ANM–
116, Transport Airplane Directorate, FAA; or
the European Aviation Safety Agency
(EASA); or Airbus’s EASA Design
Organization Approval (DOA). If approved by
the DOA, the approval must include the
DOA-authorized signature.
(3) Required for Compliance (RC): Except
as provide by paragraph (j) of this AD, if any
service information contains procedures or
tests that are identified as RC, those
procedures and tests must be done to comply
with this AD; any procedures or tests that are
not identified as RC are recommended. Those
procedures and tests that are not identified
as RC may be deviated from using accepted
methods in accordance with the operator’s
maintenance or inspection program without
obtaining approval of an AMOC, provided
the procedures and tests identified as RC can
be done and the airplane can be put back in
an airworthy condition. Any substitutions or
changes to procedures or tests identified as
RC require approval of an AMOC.
(n) Related Information
(1) Refer to Continuing Airworthiness
Information (MCAI) EASA AD 2015–0194,
dated September 22, 2015, for related
information. You may examine the MCAI on
the Internet at https://www.regulations.gov by
searching for and locating Docket No. FAA–
2016–6418.
(2) For service information identified in
this AD, contact Airbus SAS, Airworthiness
Office—EAL, 1 Rond Point Maurice Bellonte,
31707 Blagnac Cedex, France; telephone: +33
5 61 93 36 96; fax: +33 5 61 93 45 80; email:
airworthiness.A330-A340@airbus.com;
Internet: https://www.airbus.com. You may
view this service information at the FAA,
Transport Airplane Directorate, 1601 Lind
Avenue SW., Renton, WA. For information
on the availability of this material at the
FAA, call 425–227–1221.
PO 00000
Frm 00003
Fmt 4702
Sfmt 4702
28035
Issued in Renton, Washington, on April 28,
2016.
Dionne Palermo,
Acting Manager, Transport Airplane
Directorate, Aircraft Certification Service.
[FR Doc. 2016–10633 Filed 5–6–16; 8:45 am]
BILLING CODE 4910–13–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 1, 11, 16, and 111
[Docket No. FDA–2015–N–0797]
The Food and Drug Administration
Food Safety Modernization Act: Focus
on Strategic Implementation of
Prevention-Oriented Import Safety
Programs; Public Meetings
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notification of public meetings.
The Food and Drug
Administration (FDA or we) is
announcing three one-day public
meetings in different regions throughout
the United States to provide importers
and other interested persons an
opportunity to have an in-depth
discussion on the implementation of the
FDA Food Safety Modernization Act
(FSMA) import safety programs (i.e.,
foreign supplier verification programs
(FSVPs) for importers of food for
humans and animals, accreditation of
third-party certification bodies, and
FDA’s Voluntary Qualified Importer
Program (VQIP)). During these meetings,
participants and key FDA subject matter
experts will discuss the next phase of
FSMA implementation related to import
safety programs, which includes
establishing the operational framework
for these programs and plans for
guidance documents, training,
education, and technical assistance. The
purpose of the regional outreach public
meetings is to continue the dialogue
with the importer community on FSMA
and elicit ideas that will help to inform
FDA and our stakeholders on how to
continue to work together to
successfully comply with FSMA
mandates and regulations.
DATES: See section III for dates and
times of the regional outreach meetings,
closing dates for advance registration,
and requests for special
accommodations due to disability.
ADDRESSES: See section III for meeting
locations.
SUMMARY:
FOR FURTHER INFORMATION CONTACT:
E:\FR\FM\09MYP1.SGM
09MYP1
28036
Federal Register / Vol. 81, No. 89 / Monday, May 9, 2016 / Proposed Rules
For questions about registering for the
meeting, or to register by phone: Peggy
Walker, Planning Professionals Ltd.,
1210 West McDermott St., Suite 111,
Allen, TX 75013, 214–384–0667, FAX:
469–854–6992, email: pwalker@
planningprofessionals.com.
For general questions about the
meeting or for special accommodations
due to a disability: Juanita Yates, Center
for Food Safety and Applied Nutrition
(HFS–009), Food and Drug
Administration, 5100 Paint Branch
Pkwy., College Park, MD 20740, 240–
402–1731, email: Juanita.yates@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
On May 2, 2014, we released our
‘‘Operational Strategy for Implementing
the FDA Food Safety Modernization Act
(FSMA),’’ electronically at https://
www.fda.gov/Food/Guidance
Regulation/FSMA/ucm395105.htm, to
guide the next phase of FSMA
implementation following the
establishment of regulations and
relevant programs. Within the
‘‘Operational Strategy for Implementing
FSMA,’’ there is an appendix that
outlines guiding principles for how the
operational strategy can be implemented
with respect to food and feed facilities,
produce safety standards, and import
oversight. The guiding principles
include the following: Expanding
inspection and surveillance;
administering new administrative
enforcement tools; developing guidance,
education, and technical assistance
tools; and building a preventionoriented import system.
On April 23, 2015, FDA hosted a
public meeting as an opportunity for
interested persons to share views
concerning how FDA should address
the operational aspects of FSMA
implementation as suggested by the
guiding principles. We provided an
update on current planning efforts and
received input from the public to inform
the development of operational work
plans in the areas of produce safety,
preventive controls for foods for
humans and animals, measures to
address intentional adulteration, FSVP,
and the FDA third-party accreditation
program. In addition, we established a
docket to obtain comments on a range
of operational issues that we might
consider in our FSMA implementation
approach.
On March 21, 2016, FDA hosted a
kick-off public meeting to brief
participants on the key components of
the FSVP and third-party certification
final rules; brief participants on the
status of the VQIP; discuss the plans for
guidance documents related to import
safety, as well as training, education,
and technical assistance; provide an
update on the development of a riskbased industry oversight framework that
is at the core of FSMA; and answer
questions about these import programs.
The public meeting was an opportunity
for FDA to share its current thinking on
implementation plans for programs
related to import safety. During that
public meeting, we mentioned plans to
continue dialogue on implementation of
these import safety programs with a
series of regional meeting across the
United States.
The agendas, recordings, and
transcripts for the FSMA
implementation and preventionoriented import system public meetings
are accessible on our FSMA Web site at
https://www.fda.gov/FSMA.
II. Purpose and Format of the Regional
Outreach Meetings
FDA plans to hold three one-day
public meetings in different regions
throughout the United States to provide
importers and other interested persons
an opportunity to have an in-depth
discussion on the implementation of
FSMA import safety programs (i.e.,
FSVPs for importers of food for humans
and animals, accreditation of third-party
certification bodies, and FDA’s VQIP).
We invite the public to provide
information, share experiences, and
raise issues on implementation topics
related to import safety including (but
not limited to): Increasing awareness/
reaching the regulated community,
potential partners on outreach and
implementation, state of readiness,
barriers to implementation, training and
education for industry and regulators,
guidance needs, promotion of best
practices, technical assistance,
compliance and enforcement issues, and
long-term implementation success. The
purpose of the regional outreach
meetings is to continue the dialogue
with the importer community and elicit
ideas that will help to inform FDA and
the regulated population on how to
continue to work together to
successfully comply with FSMA
mandates and regulations.
III. How To Participate in the Public
Meeting
We are holding three one-day public
meetings in different regions throughout
the United States.
Due to limited space and time, we
encourage all persons who wish to
attend the meeting to register in
advance. There is no fee to register for
the regional outreach meetings, and
registration will be on a first-come, firstserved basis. Early registration is
recommended because seating is very
limited.
Table 1 provides information on
participation in the regional outreach
meetings.
TABLE 1—INFORMATION ON PARTICIPATION IN THE MEETING
Date
Address
Preregister
Electronic address
Special
accommodations
Other
information
California Regional
Outreach Meeting.
June 7, 2016, from
8:30 a.m. to 3
p.m. PDT.
The Hilton Costa
Mesa, 3050
Bristol Street,
Costa Mesa, CA
92626.
May 26, 2016:
Closing date for
Registration.
Please
preregister
at
https://
www.fda.gov/Food/NewsEvents/
WorkshopsMeetingsConferences/
default.htm.
June 15, 2016,
from 8:30 a.m.
to 3 p.m. EDT.
Renaissance
Meadowlands
Hotel, 801 Rutherford Avenue,
Rutherford, NJ
07070.
June 3, 2016:
Closing date for
Registration.
Please
preregister
at
https://
www.fda.gov/Food/NewsEvents/
WorkshopsMeetingsConferences/
default.htm.
May 25, 2016:
Closing date to
request special
accommodations
due to a disability.
June 2, 2016:
Closing date to
request special
accommodations
due to a disability.
Registration
check-in begins at 8
a.m.
New Jersey Regional
Outreach Meeting.
mstockstill on DSK3G9T082PROD with PROPOSALS
Regional outreach
meetings
VerDate Sep<11>2014
16:16 May 06, 2016
Jkt 238001
PO 00000
Frm 00004
Fmt 4702
Sfmt 4702
E:\FR\FM\09MYP1.SGM
09MYP1
Registration
check-in begins at 8
a.m.
Federal Register / Vol. 81, No. 89 / Monday, May 9, 2016 / Proposed Rules
28037
TABLE 1—INFORMATION ON PARTICIPATION IN THE MEETING—Continued
Regional outreach
meetings
Michigan Regional
Outreach Meeting.
Address
Preregister
Electronic address
Special
accommodations
Other
information
Double Tree
Suites by Hilton
Hotel Detroit—
Downtown Fort
Shelby, 525 W
Lafayette Blvd.,
Detroit, MI
48226.
June 10, 2016:
Closing date for
Registration.
Please
preregister
at
https://
www.fda.gov/Food/NewsEvents/
WorkshopsMeetingsConferences/
default.htm.
June 9, 2016:
Closing date to
request special
accommodations
due to a disability.
Registration
check-in begins at 8
a.m.
Date
June 21, 2016,
from 8:30 a.m.
to 3 p.m. EDT.
1 You may also register via email, mail, or fax. Please include your name, title, firm name, address, and phone and fax numbers in your registration information and
send to: Peggy Walker, Planning Professionals Ltd., 1210 West McDermott St., Suite 111, Allen, TX 75013, 214–384–0667, FAX: 469–854–6992, email: pwalker@
planningprofessionals.com.
Dated: May 4, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016–10799 Filed 5–6–16; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HOUSING AND
URBAN DEVELOPMENT
24 CFR Parts 1000, 1003, 1005, 1006,
and 1007
[Docket No. FR 5861–P–01]
RIN 2577–AC96
Equal Access to Housing in HUD’s
Native American and Native Hawaiian
Programs—Regardless of Sexual
Orientation or Gender Identity
Office of the Assistant
Secretary for Public and Indian
Housing, HUD.
ACTION: Proposed rule.
AGENCY:
This proposed rule would
revise regulations for HUD’s Native
American and Native Hawaiian
programs to incorporate existing rules
that require HUD programs to be open
to all eligible individuals and families
regardless of sexual orientation, gender
identity, or marital status. Since HUD
promulgated the ‘‘Equal Access to
Housing in HUD Programs Regardless of
Sexual Orientation or Gender Identity’’
final rule in February, 2012, HUD has
required that HUD-assisted and HUDinsured housing be made available in
accordance with program eligibility
requirements and without regard to
sexual orientation, gender identity, or
marital status, and has generally
prohibited inquiries into sexual
orientation or gender identity. In
applying these non-discrimination
requirements to HUD’s Native American
and Native Hawaiian programs, this
proposed rule would further the Federal
goal of providing decent housing and a
suitable living environment for all.
DATES: Comments due: July 8, 2016.
mstockstill on DSK3G9T082PROD with PROPOSALS
SUMMARY:
VerDate Sep<11>2014
16:16 May 06, 2016
Jkt 238001
Interested persons are
invited to submit comments regarding
this proposed rule to the Regulations
Division, Office of General Counsel,
Department of Housing and Urban
Development, 451 7th Street SW., Room
10276, Washington, DC 20410–0500.
Communications must refer to the above
docket number and title. There are two
methods for submitting public
comments. All submissions must refer
to the above docket number and title.
1. Submission of Comments by Mail.
Comments may be submitted by mail to
the Regulations Division, Office of
General Counsel, Department of
Housing and Urban Development, 451
7th Street SW., Room 10276,
Washington, DC 20410–0500.
2. Electronic Submission of
Comments. Interested persons may
submit comments electronically through
the Federal eRulemaking Portal at
www.regulations.gov. HUD strongly
encourages commenters to submit
comments electronically. Electronic
submission of comments allows the
commenter maximum time to prepare
and submit a comment, ensures timely
receipt by HUD, and enables HUD to
make them immediately available to the
public. Comments submitted
electronically through the
www.regulations.gov Web site can be
viewed by other commenters and
interested members of the public.
Commenters should follow the
instructions provided on that site to
submit comments electronically.
ADDRESSES:
Note: To receive consideration as public
comments, comments must be submitted
through one of the two methods specified
above. Again, all submissions must refer to
the docket number and title of the rule.
No Facsimile Comments. Facsimile
(fax) comments are not acceptable.
Public Inspection of Public
Comments. All properly submitted
comments and communications
submitted to HUD will be available for
public inspection and copying between
8 a.m. and 5 p.m., weekdays, at the
above address. Due to security measures
PO 00000
Frm 00005
Fmt 4702
Sfmt 4702
at the HUD Headquarters building, an
advance appointment to review the
public comments must be scheduled by
calling the Regulations Division at 202–
708–3055 (this is not a toll-free
number). Individuals with speech or
hearing impairments may access this
number via TTY by calling the Federal
Relay Service, toll free, at 800–877–
8339. Copies of all comments submitted
are available for inspection and
downloading at www.regulations.gov.
FOR FURTHER INFORMATION CONTACT:
[Contact Name to be Inserted], Office of
Native American Programs, Office of
Public and Indian Housing, Department
of Housing and Urban Development,
451 7th Street SW., Room 5206,
Washington, DC 20410–8000; telephone
number 202–708–2333 (this is not a tollfree number). Persons with hearing or
speech impairments may access this
number through TTY by calling the tollfree Federal Relay Service at 800–877–
8339.
SUPPLEMENTARY INFORMATION:
I. Background
On February 3, 2012, HUD published
in the Federal Register, at 77 FR 5662,
a final rule titled ‘‘Equal Access to
Housing in HUD Programs Regardless of
Sexual Orientation or Gender Identity’’
(the Equal Access Rule) in order to
address evidence that lesbian, gay,
bisexual, and transgender (LGBT)
individuals and families do not have
equal access to housing, and to promote
the federal goal of providing decent
housing and a suitable living
environment for all.1 The Equal Access
Rule requires that housing assisted or
insured by HUD be made available to
individuals and families without regard
to actual or perceived sexual
orientation, gender identity, or marital
status. Additionally, the rule prohibits
owners and administrators of HUDassisted or HUD-insured housing,
approved lenders in an FHA mortgage
1 See Section 2 of the Housing Act of 1949 at 42
U.S.C. 1441 (Congressional Declaration of National
Housing Policy).
E:\FR\FM\09MYP1.SGM
09MYP1
]]>Agencies
[Federal Register Volume 81, Number 89 (Monday, May 9, 2016)]
[Proposed Rules]
[Pages 28035-28037]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-10799]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 1, 11, 16, and 111
[Docket No. FDA-2015-N-0797]
The Food and Drug Administration Food Safety Modernization Act:
Focus on Strategic Implementation of Prevention-Oriented Import Safety
Programs; Public Meetings
AGENCY: Food and Drug Administration, HHS.
ACTION: Notification of public meetings.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or we) is announcing
three one-day public meetings in different regions throughout the
United States to provide importers and other interested persons an
opportunity to have an in-depth discussion on the implementation of the
FDA Food Safety Modernization Act (FSMA) import safety programs (i.e.,
foreign supplier verification programs (FSVPs) for importers of food
for humans and animals, accreditation of third-party certification
bodies, and FDA's Voluntary Qualified Importer Program (VQIP)). During
these meetings, participants and key FDA subject matter experts will
discuss the next phase of FSMA implementation related to import safety
programs, which includes establishing the operational framework for
these programs and plans for guidance documents, training, education,
and technical assistance. The purpose of the regional outreach public
meetings is to continue the dialogue with the importer community on
FSMA and elicit ideas that will help to inform FDA and our stakeholders
on how to continue to work together to successfully comply with FSMA
mandates and regulations.
DATES: See section III for dates and times of the regional outreach
meetings, closing dates for advance registration, and requests for
special accommodations due to disability.
ADDRESSES: See section III for meeting locations.
FOR FURTHER INFORMATION CONTACT:
[[Page 28036]]
For questions about registering for the meeting, or to register by
phone: Peggy Walker, Planning Professionals Ltd., 1210 West McDermott
St., Suite 111, Allen, TX 75013, 214-384-0667, FAX: 469-854-6992,
email: pwalker@planningprofessionals.com.
For general questions about the meeting or for special
accommodations due to a disability: Juanita Yates, Center for Food
Safety and Applied Nutrition (HFS-009), Food and Drug Administration,
5100 Paint Branch Pkwy., College Park, MD 20740, 240-402-1731, email:
Juanita.yates@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
On May 2, 2014, we released our ``Operational Strategy for
Implementing the FDA Food Safety Modernization Act (FSMA),''
electronically at https://www.fda.gov/Food/GuidanceRegulation/FSMA/ucm395105.htm, to guide the next phase of FSMA implementation following
the establishment of regulations and relevant programs. Within the
``Operational Strategy for Implementing FSMA,'' there is an appendix
that outlines guiding principles for how the operational strategy can
be implemented with respect to food and feed facilities, produce safety
standards, and import oversight. The guiding principles include the
following: Expanding inspection and surveillance; administering new
administrative enforcement tools; developing guidance, education, and
technical assistance tools; and building a prevention-oriented import
system.
On April 23, 2015, FDA hosted a public meeting as an opportunity
for interested persons to share views concerning how FDA should address
the operational aspects of FSMA implementation as suggested by the
guiding principles. We provided an update on current planning efforts
and received input from the public to inform the development of
operational work plans in the areas of produce safety, preventive
controls for foods for humans and animals, measures to address
intentional adulteration, FSVP, and the FDA third-party accreditation
program. In addition, we established a docket to obtain comments on a
range of operational issues that we might consider in our FSMA
implementation approach.
On March 21, 2016, FDA hosted a kick-off public meeting to brief
participants on the key components of the FSVP and third-party
certification final rules; brief participants on the status of the
VQIP; discuss the plans for guidance documents related to import
safety, as well as training, education, and technical assistance;
provide an update on the development of a risk-based industry oversight
framework that is at the core of FSMA; and answer questions about these
import programs. The public meeting was an opportunity for FDA to share
its current thinking on implementation plans for programs related to
import safety. During that public meeting, we mentioned plans to
continue dialogue on implementation of these import safety programs
with a series of regional meeting across the United States.
The agendas, recordings, and transcripts for the FSMA
implementation and prevention-oriented import system public meetings
are accessible on our FSMA Web site at https://www.fda.gov/FSMA.
II. Purpose and Format of the Regional Outreach Meetings
FDA plans to hold three one-day public meetings in different
regions throughout the United States to provide importers and other
interested persons an opportunity to have an in-depth discussion on the
implementation of FSMA import safety programs (i.e., FSVPs for
importers of food for humans and animals, accreditation of third-party
certification bodies, and FDA's VQIP). We invite the public to provide
information, share experiences, and raise issues on implementation
topics related to import safety including (but not limited to):
Increasing awareness/reaching the regulated community, potential
partners on outreach and implementation, state of readiness, barriers
to implementation, training and education for industry and regulators,
guidance needs, promotion of best practices, technical assistance,
compliance and enforcement issues, and long-term implementation
success. The purpose of the regional outreach meetings is to continue
the dialogue with the importer community and elicit ideas that will
help to inform FDA and the regulated population on how to continue to
work together to successfully comply with FSMA mandates and
regulations.
III. How To Participate in the Public Meeting
We are holding three one-day public meetings in different regions
throughout the United States.
Due to limited space and time, we encourage all persons who wish to
attend the meeting to register in advance. There is no fee to register
for the regional outreach meetings, and registration will be on a
first-come, first-served basis. Early registration is recommended
because seating is very limited.
Table 1 provides information on participation in the regional
outreach meetings.
Table 1--Information on Participation in the Meeting
--------------------------------------------------------------------------------------------------------------------------------------------------------
Special
Regional outreach meetings Date Address Preregister Electronic address accommodations Other information
--------------------------------------------------------------------------------------------------------------------------------------------------------
California Regional Outreach June 7, 2016, from The Hilton Costa May 26, 2016: Please preregister at May 25, 2016: Registration
Meeting. 8:30 a.m. to 3 Mesa, 3050 Closing date for https://www.fda.gov/ Closing date to check-in begins
p.m. PDT. Bristol Street, Registration. Food/NewsEvents/ request special at 8 a.m.
Costa Mesa, CA WorkshopsMeetingsConf accommodations
92626. erences/default.htm. due to a
disability.
New Jersey Regional Outreach June 15, 2016, Renaissance June 3, 2016: Please preregister at June 2, 2016: Registration
Meeting. from 8:30 a.m. to Meadowlands Closing date for https://www.fda.gov/ Closing date to check-in begins
3 p.m. EDT. Hotel, 801 Registration. Food/NewsEvents/ request special at 8 a.m.
Rutherford WorkshopsMeetingsConf accommodations
Avenue, erences/default.htm. due to a
Rutherford, NJ disability.
07070.
[[Page 28037]]
Michigan Regional Outreach June 21, 2016, Double Tree Suites June 10, 2016: Please preregister at June 9, 2016: Registration
Meeting. from 8:30 a.m. to by Hilton Hotel Closing date for https://www.fda.gov/ Closing date to check-in begins
3 p.m. EDT. Detroit_Downtown Registration. Food/NewsEvents/ request special at 8 a.m.
Fort Shelby, 525 WorkshopsMeetingsConf accommodations
W Lafayette erences/default.htm. due to a
Blvd., Detroit, disability.
MI 48226.
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\1\ You may also register via email, mail, or fax. Please include your name, title, firm name, address, and phone and fax numbers in your registration
information and send to: Peggy Walker, Planning Professionals Ltd., 1210 West McDermott St., Suite 111, Allen, TX 75013, 214-384-0667, FAX: 469-854-
6992, email: pwalker@planningprofessionals.com.
Dated: May 4, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016-10799 Filed 5-6-16; 8:45 am]
BILLING CODE 4164-01-P
