International Conference on Harmonisation; Draft Recommendation for the Revision of the Permitted Daily Exposure for the Solvent Cumene According to the Maintenance Procedures for the Guidance Q3C Impurities: Residual Solvents; Availability, 42098-42099 [2010-17618]
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Federal Register / Vol. 75, No. 138 / Tuesday, July 20, 2010 / Notices
ESTIMATES OF HOUR BURDEN—Continued
Estimated
number of respondents
Estimated
number of responses annually per respondent
Average burden hours per
response
Estimated total
annual burden
hours
Recommendations for All Programs ................................................................
Supplemental Documents for Application ........................................................
Feedback Questions ........................................................................................
35,705
14,540
53,095
1
1
1
0.25
0.75
0.25
8,926.3
10,905.0
13,273.8
Totals ........................................................................................................
120,730
Program
Request for Comments
Written comments and/or suggestions
from the public and affected agencies
should address one or more of the
following points: (1) Evaluate whether
the proposed collection of information
is necessary for the proper performance
of the function of the agency, including
whether the information will have
practical utility; (2) Evaluate the
accuracy of the agency’s estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(3) Enhance the quality, utility, and
clarity of the information to be
collected; and (4) Minimize the burden
of the collection of information on those
who are to respond, including the use
of appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, contact: Dr. Patricia
Wagner, Director of Admissions &
Registrar, Office of Intramural Training
& Education, National Institutes of
Health, 2 Center Drive, Building 2/Room
2E06, Bethesda, Maryland 20892–0234,
or call 240–476–3619 or e-mail your
request, including your address to:
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wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1
DATES: Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 60 days of the date of
this publication.
Date: July 15, 2010.
Michael M. Gottesman,
Deputy Director for Intramural Research,
National Institutes of Health.
[FR Doc. 2010–17669 Filed 7–19–10; 8:45 am]
BILLING CODE 4140–01–P
VerDate Mar<15>2010
15:23 Jul 19, 2010
Jkt 220001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0327]
International Conference on
Harmonisation; Draft Recommendation
for the Revision of the Permitted Daily
Exposure for the Solvent Cumene
According to the Maintenance
Procedures for the Guidance Q3C
Impurities: Residual Solvents;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
availability of a draft recommendation
for the revision of the permitted daily
exposure (PDE) for the solvent cumene
according to the maintenance
procedures for the guidance for industry
entitled ‘‘Q3C: Impurities: Residual
Solvents.’’ The draft recommendation
was prepared under the auspices of the
International Conference on
Harmonisation of Technical
Requirements for Registration of
Pharmaceuticals for Human Use (ICH).
DATES: Although you can comment on
any guidance at any time (see 21 CFR
10.115(g)(5)), to ensure that the agency
considers your comment on this draft
recommendation before it begins work
on the final recommendation, submit
either electronic or written comments
on the document by September 20,
2010.
ADDRESSES: Submit written requests for
single copies of the draft
recommendation to the Division of Drug
Information (HFD–240), Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, rm. 2201,
Silver Spring, MD 20993–0002, or the
Office of Communication, Outreach and
Development (HFM–40), Center for
Biologics Evaluation and Research
(CBER), Food and Drug Administration,
1401 Rockville Pike, suite 200N,
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
46,147.5
Rockville, MD 20852–1448. Send one
self-addressed adhesive label to assist
the office in processing your requests.
The draft recommendation may also be
obtained by mail by calling CBER at 1–
800–835–4709 or 301–827–1800. See
the SUPPLEMENTARY INFORMATION section
for electronic access to the draft
recommendation.
Submit electronic comments on the
draft recommendation to https://
www.regulations.gov. Submit written
comments to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Regarding the guidance: David
Jacobson-Kram, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Silver Spring, MD
20993, 301–796–0175.
Regarding the ICH: Michelle Limoli,
Office of International Programs
(HFG–1), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–
4480.
SUPPLEMENTARY INFORMATION:
I. Background
In recent years, many important
initiatives have been undertaken by
regulatory authorities and industry
associations to promote international
harmonization of regulatory
requirements. FDA has participated in
many meetings designed to enhance
harmonization and is committed to
seeking scientifically based harmonized
technical procedures for pharmaceutical
development. One of the goals of
harmonization is to identify and then
reduce differences in technical
requirements for drug development
among regulatory agencies.
ICH was organized to provide an
opportunity for tripartite harmonization
initiatives to be developed with input
from both regulatory and industry
representatives. FDA also seeks input
from consumer representatives and
others. ICH is concerned with
E:\FR\FM\20JYN1.SGM
20JYN1
wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1
Federal Register / Vol. 75, No. 138 / Tuesday, July 20, 2010 / Notices
harmonization of technical
requirements for the registration of
pharmaceutical products among three
regions: The European Union, Japan,
and the United States. The six ICH
sponsors are the European Commission;
the European Federation of
Pharmaceutical Industries Associations;
the Japanese Ministry of Health, Labour,
and Welfare; the Japanese
Pharmaceutical Manufacturers
Association; the Centers for Drug
Evaluation and Research and Biologics
Evaluation and Research, FDA; and the
Pharmaceutical Research and
Manufacturers of America. The ICH
Secretariat, which coordinates the
preparation of documentation, is
provided by the International
Federation of Pharmaceutical
Manufacturers Associations (IFPMA).
The ICH Steering Committee includes
representatives from each of the ICH
sponsors and the IFPMA, as well as
observers from the World Health
Organization, Health Canada, and the
European Free Trade Area.
In the Federal Register of December
24, 1997 (62 FR 67377), FDA published
the ICH guidance for industry entitled
‘‘Q3C Impurities: Residual Solvents.’’
The guidance makes recommendations
as to what amounts of residual solvents
are considered safe in pharmaceuticals.
The guidance recommends use of less
toxic solvents and describes levels
considered to be toxicologically
acceptable for some residual solvents.
Upon issuance in 1997, the text and
appendix 1 of the guidance contained
several tables and a list of solvents
categorizing residual solvents by
toxicity, classes 1 through 3, with class
1 being the most toxic. The ICH Quality
Expert Working Group (EWG) agreed
that the PDE could be modified if
reliable and more relevant toxicity data
were brought to the attention of the
group and the modified PDE could
result in a revision of the tables and list.
In 1999, ICH instituted a Q3C
maintenance agreement and formed a
maintenance EWG (Q3C EWG). The
agreement provided for the revisitation
of solvent PDEs and allowed for minor
changes to the tables and list that
include the existing PDEs. The
agreement also provided that new
solvents and PDEs could be added to the
tables and list based on adequate
toxicity data. In the Federal Register of
February 12, 2002 (67 FR 6542), FDA
briefly described the process for
proposing future revisions to the PDE.
In the same notice, the agency
announced its decision to delink the
tables and list from the Q3C guidance
and create a stand alone document
entitled ‘‘Q3C: Tables and List’’ to
VerDate Mar<15>2010
15:23 Jul 19, 2010
Jkt 220001
facilitate making changes recommended
by ICH.
II. Draft Recommendation to Revise the
PDE for Cumene
In March 2010, the ICH Steering
Committee agreed that a draft
recommendation to revise the PDE for
the solvent cumene should be made
available for public comment. The draft
recommendation is the product of the
Q3C EWG of the ICH. Comments about
this draft will be considered by FDA
and the Q3C EWG.
The draft recommendation addresses
the safety classification of cumene.
When the Q3C guidance was published
in 1997, cumene was listed as a class 3
solvent (i.e., a solvent with low
toxicity). The Q3C EWG has reviewed
new toxicity data derived from a
carcinogenicity study performed by the
National Toxicology Program. The new
data suggest a positive systemic
carcinogenic effect, and this observation
raises the toxicity associated with this
solvent. In March 2010, the ICH Steering
Committee was briefed on the results of
the Q3C EWG’s analysis. The
recommendation was to move cumene
from class 3 into class 2. The analysis
and draft recommendation are available
for review on the Internet (see section IV
of this document).
This draft recommendation is being
issued consistent with FDA’s good
guidance practices regulation (21 CFR
10.115). The draft recommendation for
the solvent cumene, when finalized,
will represent the agency’s current
thinking on this topic. 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 statutes
and regulations.
III. Comments
Interested persons may submit to the
Division of Dockets Management (see
ADDRESSES) either electronic or written
comments regarding this document. It is
only necessary to send one set of
comments. It is no longer necessary to
send two copies of mailed comments.
Identify comments with the docket
number found in brackets in the
heading of this document. The draft
recommendation and received
comments may be seen in the Division
of Dockets Management between 9 a.m.
and 4 p.m., Monday through Friday.
IV. Electronic Access to Documents and
the Maintenance Procedures
Persons with access to the Internet
may obtain the Q3C guidance
documents at https://
PO 00000
Frm 00033
Fmt 4703
Sfmt 4703
42099
www.regulations.gov, https://
www.fda.gov/Drugs/Guidance
ComplianceRegulatoryInformation/
Guidances/default.htm, or https://
www.fda.gov/BiologicsBloodVaccines/
GuidanceComplianceRegulatory
Information/Guidances/default.htm.
Information on the Q3C maintenance
process as well as proposals, data
analysis, and draft and final
recommendations for revisions to the
tables and list are available at https://
www.fda.gov/Drugs/Guidance
ComplianceRegulatoryInformation/
Guidances/ucm125820.htm.
Dated: July 9, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–17618 Filed 7–19–10; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Eunice Kennedy Shriver National
Institute of Child Health and Human
Development; Notice of Closed
Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The contract proposals and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the contract
proposals, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Child Health and Human Development
Special Emphasis Panel Assays of Biological
Specimens for Division of Epidemiology,
Statistical and Prevention Research.
Date: August 10, 2010.
Time: 2 p.m. to 4 p.m.
Agenda: To review and evaluate contract
proposals.
Place: National Institutes of Health, 6100
Executive Boulevard, Rockville, MD 20852.
(Telephone Conference Call)
Contact Person: Sathasiva B. Kandasamy,
PhD, Scientific Review Officer, Division of
Scientific Review, Eunice Kennedy Shriver
National Institute of Child Health and
Human Development, NIH, 6100 Executive
Blvd., Room 5B01, Bethesda, MD 20892–
9304. 301–435–6680.
skandasa@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.864, Population Research;
E:\FR\FM\20JYN1.SGM
20JYN1
Agencies
[Federal Register Volume 75, Number 138 (Tuesday, July 20, 2010)]
[Notices]
[Pages 42098-42099]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-17618]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2010-N-0327]
International Conference on Harmonisation; Draft Recommendation
for the Revision of the Permitted Daily Exposure for the Solvent Cumene
According to the Maintenance Procedures for the Guidance Q3C
Impurities: Residual Solvents; Availability
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing the
availability of a draft recommendation for the revision of the
permitted daily exposure (PDE) for the solvent cumene according to the
maintenance procedures for the guidance for industry entitled ``Q3C:
Impurities: Residual Solvents.'' The draft recommendation was prepared
under the auspices of the International Conference on Harmonisation of
Technical Requirements for Registration of Pharmaceuticals for Human
Use (ICH).
DATES: Although you can comment on any guidance at any time (see 21 CFR
10.115(g)(5)), to ensure that the agency considers your comment on this
draft recommendation before it begins work on the final recommendation,
submit either electronic or written comments on the document by
September 20, 2010.
ADDRESSES: Submit written requests for single copies of the draft
recommendation to the Division of Drug Information (HFD-240), Center
for Drug Evaluation and Research, Food and Drug Administration, 10903
New Hampshire Ave., Bldg. 51, rm. 2201, Silver Spring, MD 20993-0002,
or the Office of Communication, Outreach and Development (HFM-40),
Center for Biologics Evaluation and Research (CBER), Food and Drug
Administration, 1401 Rockville Pike, suite 200N, Rockville, MD 20852-
1448. Send one self-addressed adhesive label to assist the office in
processing your requests. The draft recommendation may also be obtained
by mail by calling CBER at 1-800-835-4709 or 301-827-1800. See the
SUPPLEMENTARY INFORMATION section for electronic access to the draft
recommendation.
Submit electronic comments on the draft recommendation to https://www.regulations.gov. Submit written comments to the Division of Dockets
Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane,
rm. 1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Regarding the guidance: David Jacobson-Kram, Center for Drug
Evaluation and Research, Food and Drug Administration, 10903 New
Hampshire Ave., Silver Spring, MD 20993, 301-796-0175.
Regarding the ICH: Michelle Limoli, Office of International
Programs (HFG-1), Food and Drug Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301-827-4480.
SUPPLEMENTARY INFORMATION:
I. Background
In recent years, many important initiatives have been undertaken by
regulatory authorities and industry associations to promote
international harmonization of regulatory requirements. FDA has
participated in many meetings designed to enhance harmonization and is
committed to seeking scientifically based harmonized technical
procedures for pharmaceutical development. One of the goals of
harmonization is to identify and then reduce differences in technical
requirements for drug development among regulatory agencies.
ICH was organized to provide an opportunity for tripartite
harmonization initiatives to be developed with input from both
regulatory and industry representatives. FDA also seeks input from
consumer representatives and others. ICH is concerned with
[[Page 42099]]
harmonization of technical requirements for the registration of
pharmaceutical products among three regions: The European Union, Japan,
and the United States. The six ICH sponsors are the European
Commission; the European Federation of Pharmaceutical Industries
Associations; the Japanese Ministry of Health, Labour, and Welfare; the
Japanese Pharmaceutical Manufacturers Association; the Centers for Drug
Evaluation and Research and Biologics Evaluation and Research, FDA; and
the Pharmaceutical Research and Manufacturers of America. The ICH
Secretariat, which coordinates the preparation of documentation, is
provided by the International Federation of Pharmaceutical
Manufacturers Associations (IFPMA).
The ICH Steering Committee includes representatives from each of
the ICH sponsors and the IFPMA, as well as observers from the World
Health Organization, Health Canada, and the European Free Trade Area.
In the Federal Register of December 24, 1997 (62 FR 67377), FDA
published the ICH guidance for industry entitled ``Q3C Impurities:
Residual Solvents.'' The guidance makes recommendations as to what
amounts of residual solvents are considered safe in pharmaceuticals.
The guidance recommends use of less toxic solvents and describes levels
considered to be toxicologically acceptable for some residual solvents.
Upon issuance in 1997, the text and appendix 1 of the guidance
contained several tables and a list of solvents categorizing residual
solvents by toxicity, classes 1 through 3, with class 1 being the most
toxic. The ICH Quality Expert Working Group (EWG) agreed that the PDE
could be modified if reliable and more relevant toxicity data were
brought to the attention of the group and the modified PDE could result
in a revision of the tables and list.
In 1999, ICH instituted a Q3C maintenance agreement and formed a
maintenance EWG (Q3C EWG). The agreement provided for the revisitation
of solvent PDEs and allowed for minor changes to the tables and list
that include the existing PDEs. The agreement also provided that new
solvents and PDEs could be added to the tables and list based on
adequate toxicity data. In the Federal Register of February 12, 2002
(67 FR 6542), FDA briefly described the process for proposing future
revisions to the PDE. In the same notice, the agency announced its
decision to delink the tables and list from the Q3C guidance and create
a stand alone document entitled ``Q3C: Tables and List'' to facilitate
making changes recommended by ICH.
II. Draft Recommendation to Revise the PDE for Cumene
In March 2010, the ICH Steering Committee agreed that a draft
recommendation to revise the PDE for the solvent cumene should be made
available for public comment. The draft recommendation is the product
of the Q3C EWG of the ICH. Comments about this draft will be considered
by FDA and the Q3C EWG.
The draft recommendation addresses the safety classification of
cumene. When the Q3C guidance was published in 1997, cumene was listed
as a class 3 solvent (i.e., a solvent with low toxicity). The Q3C EWG
has reviewed new toxicity data derived from a carcinogenicity study
performed by the National Toxicology Program. The new data suggest a
positive systemic carcinogenic effect, and this observation raises the
toxicity associated with this solvent. In March 2010, the ICH Steering
Committee was briefed on the results of the Q3C EWG's analysis. The
recommendation was to move cumene from class 3 into class 2. The
analysis and draft recommendation are available for review on the
Internet (see section IV of this document).
This draft recommendation is being issued consistent with FDA's
good guidance practices regulation (21 CFR 10.115). The draft
recommendation for the solvent cumene, when finalized, will represent
the agency's current thinking on this topic. 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 statutes and regulations.
III. Comments
Interested persons may submit to the Division of Dockets Management
(see ADDRESSES) either electronic or written comments regarding this
document. It is only necessary to send one set of comments. It is no
longer necessary to send two copies of mailed comments. Identify
comments with the docket number found in brackets in the heading of
this document. The draft recommendation and received comments may be
seen in the Division of Dockets Management between 9 a.m. and 4 p.m.,
Monday through Friday.
IV. Electronic Access to Documents and the Maintenance Procedures
Persons with access to the Internet may obtain the Q3C guidance
documents at https://www.regulations.gov, https://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm, or
https://www.fda.gov/BiologicsBloodVaccines/GuidanceComplianceRegulatoryInformation/Guidances/default.htm.
Information on the Q3C maintenance process as well as proposals, data
analysis, and draft and final recommendations for revisions to the
tables and list are available at https://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/ucm125820.htm.
Dated: July 9, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010-17618 Filed 7-19-10; 8:45 am]
BILLING CODE 4160-01-S