[Federal Register Volume 65, Number 203 (Thursday, October 19, 2000)]
[Notices]
[Pages 62723-62724]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 00-26897]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 00D-1532]
International Cooperation on Harmonisation of Technical
Requirements for Registration of Veterinary Medicinal Products (VICH);
Draft Guidances for Industry on ``Effectiveness of Anthelmintics:
Specific Recommendations for Equine'' (VICH GL15), ``Effectiveness of
Anthelmintics: Specific Recommendations for Porcine'' (VICH GL16), and
``Effectiveness of Anthelmintics: Specific Recommendations for Canine''
(VICH GL19); Availability; Request for Comments
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice; request for comments.
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SUMMARY: The Food and Drug Administration (FDA) is announcing the
availability for comment of three draft guidances for industry (Nos.
109, 110, and 111, respectively) entitled: ``Effectiveness of
Anthelmintics: Specific Recommendations for Equine'' (VICH GL15),
``Effectiveness of Anthelmintics: Specific Recommendations for
Porcine'' (VICH GL16), and ``Effectiveness of Anthelmintics: Specific
Recommendations for Canine'' (VICH GL19). These related draft guidance
documents have been developed by the International Cooperation on
Harmonisation of Technical Requirements for Registration of Veterinary
Medicinal Products (VICH). They are intended to standardize and
simplify methods used in the evaluation of new anthelmintics submitted
for approval to the European Union, Japan, and the United States.
DATES: Submit written comments on the draft guidances by December 18,
2000, to ensure their adequate consideration in preparation of the
final guidance document. General comments on agency guidance documents
are welcome at any time.
ADDRESSES: Copies of the draft guidances entitled ``Effectiveness of
Anthelmintics: Specific Recommendations for Equine'' (VICH GL15),
``Effectiveness of Anthelmintics: Specific Recommendations for
Porcine'' (VICH GL16), and ``Effectiveness of Anthelmintics: Specific
Recommendations for Canine'' (VICH GL19) may be obtained on the
Internet from the CVM home page at http://www.fda.gov/cvm/fda/TOCs/guideline.html. Persons without Internet access may submit written
requests for single copies of the draft guidances to the Communications
Staff (HFV-12), Center for Veterinary Medicine, Food and Drug
Administration, 7500 Standish Place, Rockville, MD 20855. Send one
self-addressed adhesive label to assist that office in processing your
requests.
Submit written comments to the Dockets Management Branch (HFA-305),
Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville,
MD 20852.
FOR FURTHER INFORMATION CONTACT:
Regarding the VICH: Sharon R. Thompson, Center for Veterinary
Medicine (HFV-3), Food and Drug Administration, 7500 Standish Pl.,
Rockville, MD 20855, 301-594-1798, e-mail: [email protected], or
Carole R. Andres, Center for Veterinary Medicine (HFV-1), Food and Drug
Administration, 7500 Standish Pl., Rockville, MD 20855, 301-827-6524,
e-mail: [email protected].
Regarding the draft guidance documents: Thomas Letonja, Center for
Veterinary Medicine (HFV-135), Food and Drug Administration, 7500
Standish Pl., Rockville, MD 20855, 301-827-7576, e-mail:
[email protected].
SUPPLEMENTARY INFORMATION:
I. Background
In recent years, many important initiatives have been undertaken by
regulatory authorities and industry associations to promote the
international harmonization of regulatory requirements. FDA has
participated in efforts to enhance harmonization and has expressed its
commitment to seek scientifically based harmonized technical
requirements for the development of pharmaceutical products. One of the
goals of harmonization is to identify and then reduce the differences
in technical requirements for drug development among regulatory
agencies in different countries.
FDA has actively participated in the International Conference on
Harmonisation (ICH) of Technical Requirements for Registration of
Pharmaceuticals for Human Use for several years to develop harmonized
technical requirements for the approval of human pharmaceutical and
biological products among the European Union, Japan, and the United
States. The VICH is a parallel initiative for veterinary medicinal
products. The VICH is concerned with developing harmonized technical
requirements for the approval of veterinary medicinal products in the
[[Page 62724]]
European Union, Japan, and the United States, and includes input from
both regulatory and industry representatives.
The VICH Steering Committee is composed of member representatives
from the: European Commission; European Medicines Evaluation Agency;
European Federation of Animal Health; Committee on Veterinary Medicinal
Products; U.S. FDA; U.S. Department of Agriculture; Animal Health
Institute; Japanese Veterinary Pharmaceutical Association; Japanese
Association of Veterinary Biologics; and Japanese Ministry of
Agriculture, Forestry, and Fisheries.
Two observers are eligible to participate in the VICH Steering
Committee: One representative from the Government of Australia/New
Zealand and one representative from the industry in Australia/New
Zealand. The VICH Secretariat, which coordinates the preparation of
documentation, is provided by the Confederation Mondiale de L'Industrie
de la Sante Animale (COMISA). A COMISA representative also participates
in the VICH Steering Committee meetings.
The VICH Steering Committee held a meeting on November 16 through
19, 1999, and agreed that the three draft guidances entitled
``Effectiveness of Anthelmintics: Specific Recommendations for Equine''
(VICH GL15), ``Effectiveness of Anthelmintics: Specific Recommendations
for Porcine'' (VICH GL16), and ``Effectiveness of Anthelmintics:
Specific Recommendations for Canine'' (VICH GL19) should be made
available for public comment.
The three draft guidances: VICH GL15, VICH GL16, and VICH GL19,
should be read in conjunction with the ``Efficacy of Anthelmintics:
General Recommendations (EAGR)'' announced in the Federal Register of
July 16, 1999 (64 FR 38445). The draft guidances for equine, porcine,
and canine are part of the EAGR, and the aim of these three draft
guidances is to: (1) Be more specific for certain issues not discussed
in the general guidance, (2) highlight differences with the EAGR on
effectiveness data recommendations, and (3) give explanations for
disparities with the EAGR. Comments about the draft guidances will be
considered by the FDA and the VICH Anthelmintic Working Group.
Ultimately, FDA intends to adopt the VICH Steering Committee's final
guidances and publish them as future guidances.
These draft guidances, developed under the VICH process, have been
revised to conform to FDA's good guidance practices (65 FR 56468,
September 19, 2000). For example, the documents have been designated
``guidance'' rather than ``guideline.'' Because guidance documents are
not binding, unless specifically supported by statute or regulation,
mandatory words such as ``must,'' ``shall,'' and ``will'' in the
original VICH documents have been substituted with ``should.''
Similarly, words such as ``requirement'' or ``acceptable'' have been
replaced by ``recommendation'' or ``recommended'' as appropriate to the
context.
These draft guidances represent current FDA thinking on
effectiveness recommendations for certain veterinary anthelmintic
medicinal products. These draft guidances do not create or confer any
rights for or on any person and will not operate to bind FDA or the
public. An alternate method may be used as long as it satisfies the
requirements of applicable statutes and regulations.
II. Comments
These draft guidances are being distributed for comment purposes
only, and they are not intended for implementation at this time.
Interested persons may submit to the Dockets Management Branch (address
above) written comments regarding the draft guidance documents by
December 18, 2000. 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 brackets in the heading of
this document. A copy of the draft guidances and received comments may
be seen in the Dockets Management Branch between 9 a.m. and 4 p.m.,
Monday through Friday.
Dated: October 6, 2000.
Margaret M. Dotzel,
Associate Commissioner for Policy.
[FR Doc. 00-26897 Filed 10-18-00; 8:45 am]
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