[Federal Register: October 7, 2002 (Volume 67, Number 194)]
[&thnsp;Notices]
[Page 62489]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr07oc02-102]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 02D–0384]
Draft Guidance for Industry: Standardized Training Curriculum for
Application of HACCP Principles to Juice Processing; Availability
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is announcing the
availability of a draft guidance document entitled “Guidance for
Industry: Standardized Training Curriculum for Application of HACCP
Principles to Juice Processing” (the draft guidance). The draft
guidance advises juice processors of FDA's view that the first edition
of the “Juice HACCP Training Curriculum” of the Juice HACCP
Alliance (the standardized curriculum) is adequate for use in training
individuals to meet the requirements of the juice hazard analysis and
critical control point (HACCP) regulation. The draft guidance also
advises processors and educators on how the requirements of the juice
HACCP regulation may be met using the standardized curriculum or
alternative curricula for training individuals and on how they can
view, download, or purchase the standardized curriculum.
DATES: Submit written or electronic comments concerning this draft
guidance by December 6, 2002, to ensure adequate consideration in
preparation of the final guidance document. Comments on this draft
guidance may be submitted at any time.
ADDRESSES: Submit written requests for single copies of the draft
guidance to Michael E. Kashtock, (see FOR FURTHER INFORMATION CONTACT).
Send two self-addressed adhesive labels to assist that office in
processing your request. Submit written comments on the draft guidance
to the Dockets Management Branch (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
Submit electronic comments to http://www.fda.gov/dockets/ecomments. See
the SUPPLEMENTARY INFORMATION section for electronic access to the
draft guidance.
FOR FURTHER INFORMATION CONTACT: Michael E. Kashtock, Center for Food
Safety and Applied Nutrition (HFS–305), Food and Drug
Administration, 5100 Paint Branch Pkwy., College Park, MD
20740–3835, 301–436–2022, FAX
301–436–2651, e-mail: mkashtoc@cfsan.fda.gov.
SUPPLEMENTARY INFORMATION:
I. Background
FDA's juice HACCP regulation in part 120 (21 CFR part 120) includes
in §120.13 a requirement that individuals who perform certain
specified functions, e.g., developing the hazard analysis or the HACCP
plan, “shall have successfully completed training in the
application of HACCP principles to juice processing at least equivalent
to that received under standardized curriculum recognized as adequate
by the Food and Drug Administration, or shall be otherwise qualified
through job experience to perform these functions.” This draft
guidance advises juice processors of FDA's view that the first edition
of the “Juice HACCP Training Curriculum” of the Juice HACCP
Alliance (coordinated through the efforts of the National Center for
Food Safety and Technology at the Illinois Institute of Technology)
(the standardized curriculum) is adequate for use in training
individuals to meet the requirements of the juice HACCP regulation.
This guidance also advises processors and educators on how the
requirements of the juice HACCP regulation may be met using the
standardized curriculum or alternative curricula for training
individuals and on how they can view, download, or purchase the
standardized curriculum.
The draft guidance entitled “Guidance for Industry:
Standardized Training Curriculum for Application of HACCP Principles to
Juice Processing,” is being issued as a level 1 draft guidance
consistent with FDA's good guidance practices regulation (21 CFR
10.115). This draft guidance represents the agency's current thinking
on curricula for training juice processing personnel in the application
of HACCP principles to juice processing. It does not create or confer
any rights for or on any person and does not operate to bind FDA or the
public. An alternative approach may be used if such approach satisfies
the requirements of the applicable statute and regulations.
II. Comments
Interested persons may submit to the Dockets Management Branch (see
ADDRESSES) written or electronic comments on the draft guidance. Two
copies of any comments are to be submitted, except that individuals may
submit one copy. Comments are to be identified with the docket number
found in the brackets in the heading of this document. The draft
guidance and received comments may be seen in the Dockets Management
Branch between 9 a.m. and 4 p.m., Monday through Friday.
III. Electronic Access
Persons with access to the Internet may obtain the document at the
CFSAN Web site at http://www.cfsan.fda.gov/˜dms/guidance.html.
Dated: September 27, 2002.
Margaret M. Dotzel,
Associate Commissioner for Policy.
[FR Doc. 02–25391 Filed 10–4–02; 8:45 am]
BILLING CODE 4160–01–S