81 FR 58421 - Classification of Activities as Harvesting, Packing, Holding, or Manufacturing/Processing for Farms and Facilities; Draft Guidance for Industry; Availability

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration

Federal Register Volume 81, Issue 165 (August 25, 2016)

Page Range		58421-58422
FR Document		2016-20301

The Food and Drug Administration (FDA or we) is announcing the availability of a draft guidance for industry entitled ``Classification of Activities as Harvesting, Packing, Holding, or Manufacturing/ Processing for Farms and Facilities; Draft Guidance for Industry.'' The draft guidance, when finalized, will help food establishments determine whether the activities that they perform are within the ``farm'' definition established in our regulation for Registration of Food Facilities. Determining whether the activities a food establishment performs are within the ``farm'' definition plays a key role in determining whether its business is exempt from our regulations for Registration of Food Facilities, and from certain requirements in our regulations for ``Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food'' and ``Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Food for Animals.''

Federal Register, Volume 81 Issue 165 (Thursday, August 25, 2016)

[Federal Register Volume 81, Number 165 (Thursday, August 25, 2016)]
[Proposed Rules]
[Pages 58421-58422]
From the Federal Register Online [www.thefederalregister.org]
[FR Doc No: 2016-20301]

=======================================================================
-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Parts 117 and 507

[Docket No. FDA-2016-D-2373]

Classification of Activities as Harvesting, Packing, Holding, or
Manufacturing/Processing for Farms and Facilities; Draft Guidance for
Industry; Availability

AGENCY: Food and Drug Administration, HHS.

ACTION: Notification of availability.

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

SUMMARY: The Food and Drug Administration (FDA or we) is announcing the
availability of a draft guidance for industry entitled ``Classification
of Activities as Harvesting, Packing, Holding, or Manufacturing/
Processing for Farms and Facilities; Draft Guidance for Industry.'' The
draft guidance, when finalized, will help food establishments determine
whether the activities that they perform are within the ``farm''
definition established in our regulation for Registration of Food
Facilities. Determining whether the activities a food establishment
performs are within the ``farm'' definition plays a key role in
determining whether its business is exempt from our regulations for
Registration of Food Facilities, and from certain requirements in our
regulations for ``Current Good Manufacturing Practice, Hazard Analysis,
and Risk-Based Preventive Controls for Human Food'' and ``Current Good
Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive
Controls for Food for Animals.''

DATES: Although you can comment on any guidance at any time (see 21 CFR
10.115(g)(5)), to ensure that we consider your comment on the draft
guidance before we begin work on the final version of the guidance,
submit either electronic or written comments on the draft guidance by
February 21, 2017.

ADDRESSES: You may submit comments as follows:

Electronic Submissions

Submit electronic comments in the following way:
Federal eRulemaking Portal: http://www.regulations.gov.
Follow the instructions for submitting comments. Comments submitted
electronically, including attachments, to http://www.regulations.gov
will be posted to the docket unchanged. Because your comment will be
made public, you are solely responsible for ensuring that your comment
does not include any confidential information that you or a third party
may not wish to be posted, such as medical information, your or anyone
else's Social Security number, or confidential business information,
such as a manufacturing process. Please note that if you include your
name, contact information, or other information that identifies you in
the body of your comments, that information will be posted on http://www.regulations.gov.
If you want to submit a comment with confidential
information that you do not wish to be made available to the public,
submit the comment as a written/paper submission and in the manner
detailed (see ``Written/Paper Submissions'' and ``Instructions'').

Written/Paper Submissions

Submit written/paper submissions as follows:
Mail/Hand delivery/Courier (for written/paper
submissions): Division of Dockets Management (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
For written/paper comments submitted to the Division of
Dockets Management, FDA will post your comment, as well as any
attachments, except for information submitted, marked and identified,
as confidential, if submitted as detailed in ``Instructions.''
Instructions: All submissions received must include the Docket No.
FDA-2016-D-2373 for ``Classification of Activities as Harvesting,
Packing, Holding, or Manufacturing/Processing for Farms and Facilities;
Draft Guidance for Industry.'' Received comments will be placed in the
docket and, except for those submitted as ``Confidential Submissions,''
publicly viewable at http://www.regulations.gov or at the Division of
Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.
Confidential Submissions--To submit a comment with
confidential information that you do not wish to be made publicly
available, submit your comments only as a written/paper submission. You
should submit two copies total. One copy will include the information
you claim to be confidential with a heading or cover note that states
``THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.'' The Agency will
review this copy, including the claimed confidential information, in
its consideration of comments. The second copy, which will have the
claimed confidential information redacted/blacked out, will be
available for public viewing and posted on http://www.regulations.gov.
Submit both copies to the Division of Dockets Management. If you do not
wish your name and contact information to be made publicly available,
you can provide this information on the cover sheet and not in the body
of your comments and you must identify this information as
``confidential.'' Any information marked as ``confidential'' will not
be disclosed except in accordance with 21 CFR 10.20 and other
applicable disclosure law. For more information about FDA's posting of
comments to public dockets, see 80 FR 56469, September 18, 2015, or
access the information at: http://www.fda.gov/regulatoryinformation/dockets/default.htm.
Docket: For access to the docket to read background documents or
the electronic and written/paper comments received, go to http://www.regulations.gov and insert the docket number, found in brackets in
the heading of this document, into the ``Search'' box and follow the
prompts

[[Page 58422]]

and/or go to the Division of Dockets Management, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
Submit written requests for single copies of the draft guidance to
the Office of Food Safety, Center for Food Safety and Applied Nutrition
(HFS-300), Food and Drug Administration, 5001 Campus Dr., College Park,
MD 20740. Send two self-addressed adhesive labels to assist that office
in processing your request. See the SUPPLEMENTARY INFORMATION section
for electronic access to the draft guidance.

FOR FURTHER INFORMATION CONTACT: Jenny Scott, Center for Food Safety
and Applied Nutrition (HFS-300), Food and Drug Administration, 5001
Campus Dr., College Park, MD 20740, 240-402-2166.

SUPPLEMENTARY INFORMATION:

I. Background

We are announcing the availability of a draft guidance for industry
entitled ``Classification of Activities as Harvesting, Packing,
Holding, or Manufacturing/Processing for Farms and Facilities.'' We are
issuing the draft guidance consistent with our good guidance practices
regulation (21 CFR 10.115). The draft guidance, when finalized, will
represent the current thinking of the FDA on this topic. It does not
establish any rights for any person and is not binding on FDA or the
public. You can use an alternate approach if it satisfies the
requirements of the applicable statutes and regulations.
Section 103(c) of the FDA Food Safety Modernization Act (FSMA)
directed us to conduct rulemaking to clarify the on-farm activities
that would, in part, determine when an establishment is required to
register with us as a ``facility,'' or is not required to register with
us because the establishment is a ``farm.'' To do so, we conducted
rulemaking to revise and add farm-related definitions to our existing
regulation for Registration of Food Facilities in the same rulemaking
documents that we issued to establish our regulation entitled ``Current
Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive
Controls for Human Food'' in part 117 (21 CFR part 117). (See the final
rule at 80 FR 55908, September 17, 2015). For the purposes of the draft
guidance, we call that rulemaking ``the farm definition rulemaking.''
The farm definition rulemaking revised the ``farm'' definition to
provide for two types of farms: (1) Primary production farms and (2)
secondary activities farms. The farm definition rulemaking also revised
three definitions associated with the ``farm'' definition (i.e., the
definitions of ``packing,'' ``holding,'' and ``manufacturing/
processing'') and added more examples of activities in each of these
definitions. The farm definition rulemaking also established a new
definition associated with the ``farm'' definition (i.e., the
definition of ``harvesting'') and included examples of harvesting
activities in the definition. During the farm definition rulemaking,
several comments asked us to classify specific on-farm activities as
harvesting, packing, holding, or manufacturing/processing so that an
operation that conducts these activities on a farm can determine
whether conducting that specific activity is within, or outside, the
``farm'' definition. Some comments asked us to make a table of
activities prominently available on our Internet site for easy access
whenever the public seeks out information regarding regulations to
which these activities apply. (See 80 FR 55908 at 55920.) To address
these comments, we announced our intent to issue a draft guidance with
our current thinking on the classification of activities as
``harvesting,'' ``packing,'' ``holding,'' or ``manufacturing/
processing'' (80 FR 55908 at 55921). The draft guidance that we are
making available implements that stated intent.
The draft guidance provides examples of activities classified as
``harvesting,'' ``packing,'' ``holding,'' or ``manufacturing/
processing,'' as well as activities classified in more than one way. We
note that the list of examples of activities classified as ``holding''
in the draft guidance does not include ``repacking and blast freezing .
. . when product is not exposed to the environment,'' despite our
statement in the farm definition rulemaking that such activities would
be considered practical necessities for distribution and therefore
``holding.'' See 80 FR 55908 at 55934 (Comment/Response 44). We made
similar statements in a related rulemaking to establish our regulation
entitled ``Current Good Manufacturing Practice, Hazard Analysis, and
Risk-Based Preventive Controls for Food for Animals'' in part 507 (21
CFR part 507) (80 FR 56170, September 17, 2015). See 80 FR 56170 at
56192 (Comment/Response 39). Our prior statements were incorrect and we
hereby withdraw them. Neither ``repacking'' nor ``blast freezing''
should be considered a ``holding'' activity. We have thought more about
what should be considered a ``practical necessity'' and are explaining
our thinking more in the draft guidance.

II. Paperwork Reduction Act of 1995

This draft guidance refers to previously approved collections of
information found in FDA regulations. These collections of information
are subject to review by the Office of Management and Budget (OMB)
under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501-3520). The
collections of information in 21 CFR part 1, subpart H have been
approved under OMB control number 0910-0502. The collections of
information in part 117 have been approved under OMB control number
0910-0751. The collections of information in 21 CFR part 507 have been
approved under OMB control number 0910-0789. The collections of
information in 21 CFR part 112 have been approved under OMB control
number 0910-0816. The collections of information in 21 CFR part 121
have been approved under OMB control number 0910-0812.

III. Electronic Access

Persons with access to the Internet may obtain the draft guidance
at either http://www.fda.gov/ForIndustry/ColorAdditives/GuidanceComplianceRegulatoryInformation/ucm153033.htm or http://www.regulations.gov. Use the FDA Web site listed in the previous
sentence to find the most current version of the guidance.

Dated: August 19, 2016.
Jeremy Sharp,
Deputy Commissioner for Policy, Planning, Legislation, and Analysis.
[FR Doc. 2016-20301 Filed 8-24-16; 8:45 am]
BILLING CODE 4164-01-P

Document Created: 2016-08-25 00:34:56
Document Modified: 2016-08-25 00:34:56

Category		Regulatory Information
Collection		Federal Register
sudoc Class		AE 2.7: GS 4.107: AE 2.106:
Publisher		Office of the Federal Register, National Archives and Records Administration
Section		Proposed Rules
Action		Notification of availability.
Dates		Although you can comment on any guidance at any time (see 21 CFR 10.115(g)(5)), to ensure that we consider your comment on the draft guidance before we begin work on the final version of the guidance, submit either electronic or written comments on the draft guidance by February 21, 2017.
Contact		Jenny Scott, Center for Food Safety and Applied Nutrition (HFS-300), Food and Drug Administration, 5001 Campus Dr., College Park, MD 20740, 240-402-2166.
FR Citation		81 FR 58421
CFR Citation		21 CFR 117 21 CFR 507

81 FR 58421 - Classification of Activities as Harvesting, Packing, Holding, or Manufacturing/Processing for Farms and Facilities; Draft Guidance for Industry; Availability

DEPARTMENT OF HEALTH AND HUMAN SERVICESFood and Drug Administration

Federal Register Volume 81, Issue 165 (August 25, 2016)

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration