Joint Public Meeting on the Use of Cell Culture Technology To Develop Products Derived From Livestock and Poultry, 46476-46478 [2018-19907]

Download as PDF 46476 Notices Federal Register Vol. 83, No. 178 Thursday, September 13, 2018 This section of the FEDERAL REGISTER contains documents other than rules or proposed rules that are applicable to the public. Notices of hearings and investigations, committee meetings, agency decisions and rulings, delegations of authority, filing of petitions and applications and agency statements of organization and functions are examples of documents appearing in this section. DEPARTMENT OF AGRICULTURE Office of the Secretary Office of the Secretary, USDA. ACTION: Notice. The U.S. Department of Agriculture (USDA) is extending the period for interested parties to submit an expression of interest for a proposed new headquarters location for the National Institute of Food and Agriculture (NIFA) and the Economic Research Service (ERS). The Department is extending the period to submit an expression of interest for 30 days. DATES: The notice of a request to submit expression of interests published on Wednesday, August 15, 2018 is being extended. Interested parties wishing to submit an expression of interest should do so in writing by October 15, 2018. ADDRESSES: Interested parties are invited to submit comments regarding this notice. All submissions must refer to ‘‘Expression of Interest’’ to ensure proper delivery. • Electronic Submission of Expression of Interest. Interested persons may submit information electronically to the following email address relocation@usda.gov. • Submission of Comments by Mail, Hand delivery, or Courier. Paper, disk, or CD–ROM submissions should be submitted to Donald K. Bice, Deputy Assistant Secretary, Office of the Assistant Secretary for Administration, USDA, Jamie L. Whitten Building, Room 240–W, 1400 Independence Ave. SW, Washington, DC 20250. FOR FURTHER INFORMATION CONTACT: Donald K. Bice, Telephone Number: (202) 720–3291. SUPPLEMENTARY INFORMATION: On Wednesday, August 15, 2018 (83 FR daltland on DSKBBV9HB2PROD with NOTICES 19:20 Sep 12, 2018 Jkt 244001 The Food Safety and Inspection Service (FSIS) and the Food and Drug Administration (FDA) are hosting a joint public meeting to discuss the potential hazards, oversight considerations, and labeling of cell cultured food products derived from livestock and poultry tissue. FSIS and FDA officials will make presentations on their roles and responsibilities relative to the production and labeling of safe and wholesome food and their respective regulatory frameworks, including their inspection systems, as a basis for discussing what oversight framework might be most appropriate for cell cultured food products derived from livestock and poultry. Representatives of industry, interested Background FSIS is the public health agency responsible for ensuring that meat, poultry, and egg products are safe, wholesome, and accurately labeled. FDA has responsibility for ensuring the safety of all other foods, including seafood (except catfish) and game animals as well as ensuring that the labels of these foods contain useful and reliable information. Animal cell culture food technology, as will be discussed at the public meeting, refers to the controlled growth of animal cells from livestock, poultry, fish, or other animals, their subsequent differentiation into various cell types, and their collection and processing into food. Full tissue formation in culture is [FR Doc. 2018–19877 Filed 9–12–18; 8:45 am] AGENCY: VerDate Sep<11>2014 Food Safety and Inspection Service, USDA; Food and Drug Administration, HHS. ACTION: Notice of public meeting; request for comments. Dated: September 7, 2018. Donald K. Bice, Deputy Assistant Secretary for Administration. Extension of Period To Submit Expression of Interest for Potential Sites for Headquarters Office Locations SUMMARY: individuals, and other stakeholders are invited to participate in the meeting. DATES: The public meeting will be held on Tuesday, October 23, 2018 from 8:30 a.m. to 4:00 p.m., and Wednesday, October 24, 2018, from 8:30 a.m. to 3:00 p.m. EDT. Submit either electronic or written comments on this public meeting by November 26, 2018. ADDRESSES: The meeting will be held at the Jefferson Auditorium in the South Building, U.S. Department of Agriculture (USDA), 1400 Independence Avenue SW, Washington, DC 20250. Attendance is free. Non-USDA employees must enter through the Wing 5 entrance on Independence Avenue. The South Building is a Federal facility and attendees should plan to take adequate time to pass through the security screening system. Attendees must show a valid photo ID to enter the building. FOR FURTHER INFORMATION CONTACT: Roxanne Smith, Director, Congressional and Public Affairs in the FSIS Office of Public Affairs and Consumer Education at (202) 720–4413 or roxanne.smith@ fsis.usda.gov; as well as Juanita Yates, Public Affairs Specialist in the FDA Center for Food Safety and Applied Nutrition at (240) 402–1731 or Juanita.yates@fda.hhs.gov. SUPPLEMENTARY INFORMATION: Further information on this meeting will be posted on the FSIS website at: https:// www.fsis.usda.gov/wps/portal/fsis/ newsroom/meetings and through the FSIS Constituent Update, and on the FDA website at: https://www.fda.gov/ Food/NewsEvents/WorkshopsMeetings Conferences/default.htm. 40499), the Department published a notice of a request for expression of interest for potential sites for headquarters office locations for NIFA and ERS. USDA is interested in exploring options to house the headquarters of NIFA and ERS jointly or in separate locations. The original deadline to submit an expression of interest was September 14, 2018. This action extends the submission period for 30 days. Submissions must now be received on or before October 15, 2018. BILLING CODE 3410–90–P DEPARTMENT OF AGRICULTURE Food Safety and Inspection Service DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FSIS–2018–0036] Joint Public Meeting on the Use of Cell Culture Technology To Develop Products Derived From Livestock and Poultry AGENCY: SUMMARY: PO 00000 Frm 00001 Fmt 4703 Sfmt 4703 E:\FR\FM\13SEN1.SGM 13SEN1 Federal Register / Vol. 83, No. 178 / Thursday, September 13, 2018 / Notices daltland on DSKBBV9HB2PROD with NOTICES an active medical research area, as well as a strong focus of commercial interest for food applications. Many companies, both domestic and foreign, are actively developing products using this technology. Some of these products are being designed to have the same or similar compositional, nutritional, and organoleptic characteristics as traditional meat and poultry products. Once produced, the harvested cells could potentially be processed, packaged, and marketed in the same, or similar, manner as traditional meat and poultry products. In the past several months, FSIS has received a significant amount of correspondence regarding the food products of animal cell culture technology. Much of the correspondence is in regard to a petition from the United States Cattlemen’s Association to FSIS requesting, among other things, that FSIS prohibit products derived from livestock and manufactured using animal cell culture technology from being labeled or marketed as ‘‘beef’’ or ‘‘meat.’’ The publication of this petition and related comments received by FSIS has brought significant attention to animal cell culture based food products. To date, FSIS has received over 6,100 comments on this petition from industry trade associations; consumer advocacy groups; firms operating in the meat, poultry, and/or cell culture based food product markets; and consumers. In recent years, FDA also has been contacted by firms interested in developing foods that incorporate cultured animal cells from various species and has had a number of stakeholder engagements on this topic. FDA, with USDA’s participation, is developing technical questions related to cell cultured food products to put before FDA’s Science Advisory Board on October 22, 2018 (notice will be published in an upcoming issue of the Federal Register). The intent of these questions is to support a process for identifying potential hazards, assessing risks, and establishing control measures appropriate to each risk for cell cultured food products. The dialogue with stakeholders at the joint public meeting that is the subject of this announcement will be informed by the FDA Science Board discussion, which will occur the previous day. Topics for Discussion at the Joint Public Meeting Given the high level of public interest, FSIS and FDA will be holding this joint public meeting in October to further discuss cell culture technology and provide the public with an opportunity VerDate Sep<11>2014 19:20 Sep 12, 2018 Jkt 244001 to provide comments. The first day of the meeting will focus primarily on the potential hazards that need to be controlled for the safe production of animal cell cultured food products and oversight considerations by regulatory agencies. The second day of the meeting will focus on labeling considerations. General topics to be covered and discussed include: • Potential hazards associated with the production of these products and a discussion on whether they are the same hazards as those associated with traditional meat and poultry products. What are the most significant sources of potential hazards for each and how are they similar and different? • Strategies to ensure that all potential hazards are identified and appropriately controlled, including consideration of various factors relevant to determining oversight activities for these products, such as: Æ Is there an effective and efficient application of pre-market programs to ensure the safety of foods produced by animal cell culture? Æ What type and frequency of inspection will be appropriate for various stages of the manufacture of these products? Æ What type and frequency of inspection will be appropriate for products that combine cell cultured food products and other ingredients (e.g., multicomponent foods like soups, protein bars that contain cell cultured protein as an ingredient, or products that contain both traditional meat or poultry as well as cell cultured ingredients, including food products of animal cell culture derived from livestock and poultry tissue)? • FSIS and FDA are actively working to reduce the duplicative and inefficient regulation of establishments and products under both agencies’ jurisdiction. How could this be done for products of animal cell culture derived from livestock and poultry? • What factors should be considered in the labeling of products of animal cell culture? Questions include: Æ Should standards of identity or criteria for statements of identity be established for these products to ensure that product names are truthful, not misleading, and sufficiently differentiate cell cultured products from traditional products? Æ Should the methods by which animal cell cultured products are produced (i.e., the culturing process be considered required information for purposes of labeling? If so, what factors should be considered in accurately describing the production methods? PO 00000 Frm 00002 Fmt 4703 Sfmt 4703 46477 Æ Should the source of the animal cells (i.e., the species from which the cell line was initiated) be considered required information for the purposes of labeling? Æ What factors should be considered in potentially allowing health, safety, and other claims in the marketing of animal cell cultured products? Æ How should products containing both animal cell cultured products and traditional meat and poultry products be labeled? Public Comments and Participation in Meetings Registration To register for the public meeting, please visit the following website: https://www.fsis.usda.gov/wps/portal/ fsis/newsroom/meetings/meetingsarchive/upcoming-meetings/meetingregistration-cell-culture-technology. Please provide complete contact information for each attendee, including name, title, affiliation, address, email, and telephone. Registration is free and voluntary and based on space availability, with priority given to early registrants. Persons interested in attending this public meeting are requested to register by Friday, October 19, 2018, although non-registered attendees may still participate subject to availability. Early registration is recommended because seating is limited. Registrants will receive confirmation of their registration. Accommodations for Persons With Disabilities To request accommodations due to a disability, please indicate any accommodations needed when registering. FSIS and FDA will provide sign language interpreters for this meeting. Attendees from the media will also be asked to identify themselves during the registration process. Public Comments: Oral Comments Stakeholders will have an opportunity to provide oral comments during the public meeting. Due to the anticipated high level of interest in the opportunity to make public comments and the limited time available to do so, FSIS and FDA encourage participants to indicate when registering if they wish to give public comment during a public comment session and which topic(s) you wish to address. FSIS and FDA will do their best to accommodate all persons who wish to express an opinion. FSIS and FDA encourage persons and groups who have similar E:\FR\FM\13SEN1.SGM 13SEN1 daltland on DSKBBV9HB2PROD with NOTICES 46478 Federal Register / Vol. 83, No. 178 / Thursday, September 13, 2018 / Notices interests to consolidate their information for presentation by a single representative and request time for a joint presentation. Speakers will be limited to making oral remarks; there will not be an opportunity to display materials such as slide shows, videos, or other media during the meeting. No commercial or promotional material will be permitted to be presented or distributed at the public meeting. All requests to make oral presentations should be received by Friday, October 19, 2018. to ask questions via a microphone in the auditorium. Public Comments: Written Comments The transcript of the proceedings from the public meeting will become part of the administrative record. As soon as the meeting transcripts are available, they will be accessible at https:// www.regulations.gov; on the FSIS website at http://www.fsis.usda.gov/ wps/portal/fsis/newsroom/meetings; or on the FDA website at https:// www.fda.gov/Food/NewsEvents/ WorkshopsMeetingsConferences/ default.htm. The transcripts may also be viewed at the FSIS Docket Room at the addressed listed above. Any stakeholder wishing to submit written comments prior to the meeting may do so, and may also submit comments after the meeting, using any of the following methods: Electronically: Go to http://www.regulations.gov/ and follow the online instructions for submitting comments to docket FSIS– 2018–0036; Mail, including CD–ROMs, etc.: Send to Docket Clerk, U.S. Department of Agriculture, Food Safety and Inspection Service, 1400 Independence Avenue SW, Mailstop 3758, Room 6065, Washington, DC 20250–3700; Hand- or courier-delivered submittals: Deliver to 1400 Independence Avenue SW, Room 6065, Washington, DC 20250–3700. Instructions: All items submitted by mail or electronic mail must include the Agency name (in this case FDA and FSIS) and docket number FSIS–2018– 0036. Comments received in response to this docket will be made available for public inspection and posted without change, including any personal information, to http:// www.regulations.gov/. Comments must be received by November 26, 2018. On July 12, 2018, FDA held a public meeting on foods produced using animal cell culture technology. Comments received in response to that meeting will be reviewed jointly by FDA and FSIS. There is no need to resubmit comments already submitted to FDA. Docket: For access to background documents or comments received, go to https://www.regulations.gov and insert docket number FSIS–2018–0036 into the ‘‘Search’’ box and follow the prompts; and/or call (202) 720–5627 to schedule a time to visit the FSIS Docket Room at 1400 Independence Avenue SW, Room 6065, Washington, DC 20250–3700. Question-and-Answer Periods Time has been allotted for audience questions after most presentations delivered during the meeting. Participants will have the opportunity VerDate Sep<11>2014 19:20 Sep 12, 2018 Jkt 244001 Streaming Webcast of the Public Meeting This public meeting will also be webcast. Webcast participants are asked to preregister at https:// www.fsis.usda.gov/wps/portal/fsis/ newsroom/meetings/meetings-archive/ upcoming-meetings/meetingregistration-cell-culture-technology. Transcripts Additional Public Notification Public awareness of all segments of rulemaking and policy development is important. Consequently, FSIS will announce this Federal Register publication online through the FSIS web page located at: http:// www.fsis.usda.gov/federal-register and on the FDA website at: https:// www.fda.gov/Food/NewsEvents/ WorkshopsMeetingsConferences/ default.htm. FSIS also will make copies of this publication available through the FSIS Constituent Update, which is used to provide information regarding FSIS policies, procedures, regulations, Federal Register notices, FSIS public meetings, and other types of information that could affect or would be of interest to our constituents and stakeholders. The Constituent Update is available on the FSIS web page. Through the web page, FSIS can provide information to a much broader, more diverse audience. In addition, FSIS offers an email subscription service which provides automatic and customized access to selected food safety news and information. This service is available at: http://www.fsis.usda.gov/subscribe. Options range from recalls to export information, regulations, directives, and notices. Customers can add or delete subscriptions themselves, and have the option to password protect their accounts. PO 00000 Frm 00003 Fmt 4703 Sfmt 4703 USDA Non-Discrimination Statement No agency, officer, or employee of the USDA shall, on the grounds of race, color, national origin, religion, sex, gender identity, sexual orientation, disability, age, marital status, family/ parental status, income derived from a public assistance program, or political beliefs, exclude from participation in, deny the benefits of, or subject to discrimination, any person in the United States under any program or activity conducted by the USDA. How To File a Complaint of Discrimination To file a complaint of discrimination, complete the USDA Program Discrimination Complaint Form, which may be accessed online at: http:// www.ocio.usda.gov/sites/default/files/ docs/2012/Complain_combined_6_8_ 12.pdf, or write a letter signed by you or your authorized representative. Send your completed complaint form or letter to USDA by mail, fax, or email: Mail: U.S. Department of Agriculture, Director, Office of Adjudication, 1400 Independence Avenue SW, Washington, DC 20250–9410. Fax: (202) 690–7442. Email: program.intake@usda.gov. Persons with disabilities who require alternative means for communication (Braille, large print, audiotape, etc.), should contact USDA’s TARGET Center at (202) 720–2600 (voice and TDD). Done at Washington, DC, on September 7, 2018. Paul Kiecker, Acting Administrator. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2018–19907 Filed 9–10–18; 4:15 pm] BILLING CODE 3410–DM–P DEPARTMENT OF COMMERCE Economics and Statistics Administration Performance Review Board Membership Economics and Statistics Administration, Department of Commerce. ACTION: Notice. AGENCY: In accordance with 5 U.S.C. 4314(c)(4), the Economics and Statistics Administration (ESA) announces the appointment of members who will serve on the ESA Performance Review Board (PRB). The purpose of the PRB is to provide fair and impartial review of senior executive service and scientific SUMMARY: E:\FR\FM\13SEN1.SGM 13SEN1

Agencies

[Federal Register Volume 83, Number 178 (Thursday, September 13, 2018)]
[Notices]
[Pages 46476-46478]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-19907]


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DEPARTMENT OF AGRICULTURE

Food Safety and Inspection Service

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FSIS-2018-0036]


Joint Public Meeting on the Use of Cell Culture Technology To 
Develop Products Derived From Livestock and Poultry

AGENCY: Food Safety and Inspection Service, USDA; Food and Drug 
Administration, HHS.

ACTION: Notice of public meeting; request for comments.

-----------------------------------------------------------------------

SUMMARY: The Food Safety and Inspection Service (FSIS) and the Food and 
Drug Administration (FDA) are hosting a joint public meeting to discuss 
the potential hazards, oversight considerations, and labeling of cell 
cultured food products derived from livestock and poultry tissue. FSIS 
and FDA officials will make presentations on their roles and 
responsibilities relative to the production and labeling of safe and 
wholesome food and their respective regulatory frameworks, including 
their inspection systems, as a basis for discussing what oversight 
framework might be most appropriate for cell cultured food products 
derived from livestock and poultry. Representatives of industry, 
interested individuals, and other stakeholders are invited to 
participate in the meeting.

DATES: The public meeting will be held on Tuesday, October 23, 2018 
from 8:30 a.m. to 4:00 p.m., and Wednesday, October 24, 2018, from 8:30 
a.m. to 3:00 p.m. EDT. Submit either electronic or written comments on 
this public meeting by November 26, 2018.

ADDRESSES: The meeting will be held at the Jefferson Auditorium in the 
South Building, U.S. Department of Agriculture (USDA), 1400 
Independence Avenue SW, Washington, DC 20250. Attendance is free. Non-
USDA employees must enter through the Wing 5 entrance on Independence 
Avenue. The South Building is a Federal facility and attendees should 
plan to take adequate time to pass through the security screening 
system. Attendees must show a valid photo ID to enter the building.

FOR FURTHER INFORMATION CONTACT: Roxanne Smith, Director, Congressional 
and Public Affairs in the FSIS Office of Public Affairs and Consumer 
Education at (202) 720-4413 or [email protected]; as well as 
Juanita Yates, Public Affairs Specialist in the FDA Center for Food 
Safety and Applied Nutrition at (240) 402-1731 or 
[email protected].

SUPPLEMENTARY INFORMATION: Further information on this meeting will be 
posted on the FSIS website at: https://www.fsis.usda.gov/wps/portal/fsis/newsroom/meetings and through the FSIS Constituent Update, and on 
the FDA website at: https://www.fda.gov/Food/NewsEvents/WorkshopsMeetingsConferences/default.htm.

Background

    FSIS is the public health agency responsible for ensuring that 
meat, poultry, and egg products are safe, wholesome, and accurately 
labeled. FDA has responsibility for ensuring the safety of all other 
foods, including seafood (except catfish) and game animals as well as 
ensuring that the labels of these foods contain useful and reliable 
information.
    Animal cell culture food technology, as will be discussed at the 
public meeting, refers to the controlled growth of animal cells from 
livestock, poultry, fish, or other animals, their subsequent 
differentiation into various cell types, and their collection and 
processing into food. Full tissue formation in culture is

[[Page 46477]]

an active medical research area, as well as a strong focus of 
commercial interest for food applications. Many companies, both 
domestic and foreign, are actively developing products using this 
technology. Some of these products are being designed to have the same 
or similar compositional, nutritional, and organoleptic characteristics 
as traditional meat and poultry products. Once produced, the harvested 
cells could potentially be processed, packaged, and marketed in the 
same, or similar, manner as traditional meat and poultry products.
    In the past several months, FSIS has received a significant amount 
of correspondence regarding the food products of animal cell culture 
technology. Much of the correspondence is in regard to a petition from 
the United States Cattlemen's Association to FSIS requesting, among 
other things, that FSIS prohibit products derived from livestock and 
manufactured using animal cell culture technology from being labeled or 
marketed as ``beef'' or ``meat.'' The publication of this petition and 
related comments received by FSIS has brought significant attention to 
animal cell culture based food products. To date, FSIS has received 
over 6,100 comments on this petition from industry trade associations; 
consumer advocacy groups; firms operating in the meat, poultry, and/or 
cell culture based food product markets; and consumers. In recent 
years, FDA also has been contacted by firms interested in developing 
foods that incorporate cultured animal cells from various species and 
has had a number of stakeholder engagements on this topic.
    FDA, with USDA's participation, is developing technical questions 
related to cell cultured food products to put before FDA's Science 
Advisory Board on October 22, 2018 (notice will be published in an 
upcoming issue of the Federal Register). The intent of these questions 
is to support a process for identifying potential hazards, assessing 
risks, and establishing control measures appropriate to each risk for 
cell cultured food products. The dialogue with stakeholders at the 
joint public meeting that is the subject of this announcement will be 
informed by the FDA Science Board discussion, which will occur the 
previous day.

Topics for Discussion at the Joint Public Meeting

    Given the high level of public interest, FSIS and FDA will be 
holding this joint public meeting in October to further discuss cell 
culture technology and provide the public with an opportunity to 
provide comments. The first day of the meeting will focus primarily on 
the potential hazards that need to be controlled for the safe 
production of animal cell cultured food products and oversight 
considerations by regulatory agencies. The second day of the meeting 
will focus on labeling considerations. General topics to be covered and 
discussed include:
     Potential hazards associated with the production of these 
products and a discussion on whether they are the same hazards as those 
associated with traditional meat and poultry products. What are the 
most significant sources of potential hazards for each and how are they 
similar and different?
     Strategies to ensure that all potential hazards are 
identified and appropriately controlled, including consideration of 
various factors relevant to determining oversight activities for these 
products, such as:
    [cir] Is there an effective and efficient application of pre-market 
programs to ensure the safety of foods produced by animal cell culture?
    [cir] What type and frequency of inspection will be appropriate for 
various stages of the manufacture of these products?
    [cir] What type and frequency of inspection will be appropriate for 
products that combine cell cultured food products and other ingredients 
(e.g., multicomponent foods like soups, protein bars that contain cell 
cultured protein as an ingredient, or products that contain both 
traditional meat or poultry as well as cell cultured ingredients, 
including food products of animal cell culture derived from livestock 
and poultry tissue)?
     FSIS and FDA are actively working to reduce the 
duplicative and inefficient regulation of establishments and products 
under both agencies' jurisdiction. How could this be done for products 
of animal cell culture derived from livestock and poultry?
     What factors should be considered in the labeling of 
products of animal cell culture? Questions include:
    [cir] Should standards of identity or criteria for statements of 
identity be established for these products to ensure that product names 
are truthful, not misleading, and sufficiently differentiate cell 
cultured products from traditional products?
    [cir] Should the methods by which animal cell cultured products are 
produced (i.e., the culturing process be considered required 
information for purposes of labeling? If so, what factors should be 
considered in accurately describing the production methods?
    [cir] Should the source of the animal cells (i.e., the species from 
which the cell line was initiated) be considered required information 
for the purposes of labeling?
    [cir] What factors should be considered in potentially allowing 
health, safety, and other claims in the marketing of animal cell 
cultured products?
    [cir] How should products containing both animal cell cultured 
products and traditional meat and poultry products be labeled?

Public Comments and Participation in Meetings

Registration

    To register for the public meeting, please visit the following 
website: https://www.fsis.usda.gov/wps/portal/fsis/newsroom/meetings/meetings-archive/upcoming-meetings/meeting-registration-cell-culture-technology. Please provide complete contact information for each 
attendee, including name, title, affiliation, address, email, and 
telephone.
    Registration is free and voluntary and based on space availability, 
with priority given to early registrants. Persons interested in 
attending this public meeting are requested to register by Friday, 
October 19, 2018, although non-registered attendees may still 
participate subject to availability. Early registration is recommended 
because seating is limited. Registrants will receive confirmation of 
their registration.

Accommodations for Persons With Disabilities

    To request accommodations due to a disability, please indicate any 
accommodations needed when registering. FSIS and FDA will provide sign 
language interpreters for this meeting.
    Attendees from the media will also be asked to identify themselves 
during the registration process.

Public Comments: Oral Comments

    Stakeholders will have an opportunity to provide oral comments 
during the public meeting. Due to the anticipated high level of 
interest in the opportunity to make public comments and the limited 
time available to do so, FSIS and FDA encourage participants to 
indicate when registering if they wish to give public comment during a 
public comment session and which topic(s) you wish to address. FSIS and 
FDA will do their best to accommodate all persons who wish to express 
an opinion. FSIS and FDA encourage persons and groups who have similar

[[Page 46478]]

interests to consolidate their information for presentation by a single 
representative and request time for a joint presentation. Speakers will 
be limited to making oral remarks; there will not be an opportunity to 
display materials such as slide shows, videos, or other media during 
the meeting. No commercial or promotional material will be permitted to 
be presented or distributed at the public meeting. All requests to make 
oral presentations should be received by Friday, October 19, 2018.

Public Comments: Written Comments

    Any stakeholder wishing to submit written comments prior to the 
meeting may do so, and may also submit comments after the meeting, 
using any of the following methods: Electronically: Go to http://www.regulations.gov/ and follow the online instructions for submitting 
comments to docket FSIS-2018-0036; Mail, including CD-ROMs, etc.: Send 
to Docket Clerk, U.S. Department of Agriculture, Food Safety and 
Inspection Service, 1400 Independence Avenue SW, Mailstop 3758, Room 
6065, Washington, DC 20250-3700; Hand- or courier-delivered submittals: 
Deliver to 1400 Independence Avenue SW, Room 6065, Washington, DC 
20250-3700.
    Instructions: All items submitted by mail or electronic mail must 
include the Agency name (in this case FDA and FSIS) and docket number 
FSIS-2018-0036. Comments received in response to this docket will be 
made available for public inspection and posted without change, 
including any personal information, to http://www.regulations.gov/. 
Comments must be received by November 26, 2018.
    On July 12, 2018, FDA held a public meeting on foods produced using 
animal cell culture technology. Comments received in response to that 
meeting will be reviewed jointly by FDA and FSIS. There is no need to 
resubmit comments already submitted to FDA.
    Docket: For access to background documents or comments received, go 
to https://www.regulations.gov and insert docket number FSIS-2018-0036 
into the ``Search'' box and follow the prompts; and/or call (202) 720-
5627 to schedule a time to visit the FSIS Docket Room at 1400 
Independence Avenue SW, Room 6065, Washington, DC 20250-3700.

Question-and-Answer Periods

    Time has been allotted for audience questions after most 
presentations delivered during the meeting. Participants will have the 
opportunity to ask questions via a microphone in the auditorium.

Streaming Webcast of the Public Meeting

    This public meeting will also be webcast. Webcast participants are 
asked to preregister at https://www.fsis.usda.gov/wps/portal/fsis/newsroom/meetings/meetings-archive/upcoming-meetings/meeting-registration-cell-culture-technology.

Transcripts

    The transcript of the proceedings from the public meeting will 
become part of the administrative record. As soon as the meeting 
transcripts are available, they will be accessible at https://www.regulations.gov; on the FSIS website at http://www.fsis.usda.gov/wps/portal/fsis/newsroom/meetings; or on the FDA website at https://www.fda.gov/Food/NewsEvents/WorkshopsMeetingsConferences/default.htm. 
The transcripts may also be viewed at the FSIS Docket Room at the 
addressed listed above.

Additional Public Notification

    Public awareness of all segments of rulemaking and policy 
development is important. Consequently, FSIS will announce this Federal 
Register publication online through the FSIS web page located at: 
http://www.fsis.usda.gov/federal-register and on the FDA website at: 
https://www.fda.gov/Food/NewsEvents/WorkshopsMeetingsConferences/default.htm.
    FSIS also will make copies of this publication available through 
the FSIS Constituent Update, which is used to provide information 
regarding FSIS policies, procedures, regulations, Federal Register 
notices, FSIS public meetings, and other types of information that 
could affect or would be of interest to our constituents and 
stakeholders. The Constituent Update is available on the FSIS web page. 
Through the web page, FSIS can provide information to a much broader, 
more diverse audience. In addition, FSIS offers an email subscription 
service which provides automatic and customized access to selected food 
safety news and information. This service is available at: http://www.fsis.usda.gov/subscribe. Options range from recalls to export 
information, regulations, directives, and notices. Customers can add or 
delete subscriptions themselves, and have the option to password 
protect their accounts.

USDA Non-Discrimination Statement

    No agency, officer, or employee of the USDA shall, on the grounds 
of race, color, national origin, religion, sex, gender identity, sexual 
orientation, disability, age, marital status, family/parental status, 
income derived from a public assistance program, or political beliefs, 
exclude from participation in, deny the benefits of, or subject to 
discrimination, any person in the United States under any program or 
activity conducted by the USDA.

How To File a Complaint of Discrimination

    To file a complaint of discrimination, complete the USDA Program 
Discrimination Complaint Form, which may be accessed online at: http://www.ocio.usda.gov/sites/default/files/docs/2012/Complain_combined_6_8_12.pdf, or write a letter signed by you or your 
authorized representative.
    Send your completed complaint form or letter to USDA by mail, fax, 
or email:
    Mail: U.S. Department of Agriculture, Director, Office of 
Adjudication, 1400 Independence Avenue SW, Washington, DC 20250-9410.
    Fax: (202) 690-7442.
    Email: [email protected].
    Persons with disabilities who require alternative means for 
communication (Braille, large print, audiotape, etc.), should contact 
USDA's TARGET Center at (202) 720-2600 (voice and TDD).

    Done at Washington, DC, on September 7, 2018.
Paul Kiecker,
Acting Administrator.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2018-19907 Filed 9-10-18; 4:15 pm]
 BILLING CODE 3410-DM-P