Draft Guidance for Industry on Residual Drug in Transdermal and Related Drug Delivery Systems; Availability, 45640-45641 [2010-19041]
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Federal Register / Vol. 75, No. 148 / Tuesday, August 3, 2010 / Notices
satisfied that the data on the cover sheet
is accurate and you have finalized the
Cover Sheet, you will be able to transmit
it electronically to FDA and you will be
able to print a copy of your cover sheet
showing your unique Payment
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Step Three—Send the Payment for
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Step Four—Please submit your
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C. Product and Sponsor Fees
By December 31, 2010, FDA will issue
invoices and payment instructions for
product and sponsor fees for FY 2011
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and payable 30 days after the issuance
of the invoices. FDA will issue invoices
in November 2012 for any products and
sponsors subject to fees for FY 2011 that
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billing.
Dated: July 29, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–19040 Filed 8–2–10; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–D–0246]
Draft Guidance for Industry on
Residual Drug in Transdermal and
Related Drug Delivery Systems;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing the
availability of a draft guidance for
industry entitled ‘‘Residual Drug in
Transdermal and Related Drug Delivery
Systems.’’ This draft guidance provides
recommendations to developers and
manufacturers of transdermal drug
delivery systems (TDDS), transmucosal
drug delivery systems (TMDS), and
topical patch products regarding use of
an appropriate scientific approach
during product design and
development—as well as during
manufacturing and product lifecycle
management—to ensure that the amount
of residual drug substance at the end of
erowe on DSK5CLS3C1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
14:41 Aug 02, 2010
Jkt 220001
the labeled use period is minimized.
The draft guidance is applicable to
investigational new drug applications
(INDs), new drug applications (NDAs),
abbreviated new drug applications
(ANDAs), and supplemental new drug
applications (sNDAs) for TDDS, TMDS,
and topical patch products.
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
guidance before it begins work on the
final version of the guidance, submit
either electronic or written comments
on the draft guidance, including
comments regarding the proposed
collection of information, by November
1, 2010.
ADDRESSES: Submit written requests for
single copies of the draft guidance to the
Division of Drug Information, Center for
Drug Evaluation and Research, Food
and Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, rm. 2201,
Silver Spring, MD 20993–0002. Send
one self-addressed adhesive label to
assist that office in processing your
requests. See the SUPPLEMENTARY
INFORMATION section for electronic
access to the draft guidance document.
Submit electronic comments on the
draft guidance to https://
www.regulations.gov. Submit written
comments on the draft guidance to the
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville,
MD 20852.
FOR FURTHER INFORMATION CONTACT:
Terrance Ocheltree, Center for Drug
Evaluation and Research, Food and
Drug Administration, Bldg. 21, rm.
1609, 10903 New Hampshire Ave.,
Silver Spring, MD 20993–0002, 301–
796–1988.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is announcing the availability of
a draft guidance for industry entitled
‘‘Residual Drug in Transdermal and
Related Drug Delivery Systems.’’ This
draft guidance provides
recommendations to developers and
manufacturers of TDDS, TMDS, and
topical patch products regarding use of
an appropriate scientific approach
during product design and
development—as well as during
manufacturing and product lifecycle
management—to ensure that the amount
of residual drug substance at the end of
the labeled use period is minimized.
Existing TDDS, TMDS, and topical
patches contain a larger amount of the
drug substance than what is intended to
be delivered to the patient. This excess
PO 00000
Frm 00041
Fmt 4703
Sfmt 4703
amount of drug substance is needed to
facilitate delivery of the intended
amount of the drug to the patient and
remains as residual drug in the used
system. The amount of residual drug
substance in TDDS, TMDS, and topical
patches has a significant potential to
impact the products’ quality, safety, and
efficacy. Consequently, it is necessary to
ensure that an appropriate scientific
approach is used to design and develop
these products. The approach should
ensure that the amount of residual drug
substance is minimized consistent with
the current state of technology.
Currently marketed TDDS, TMDS,
and topical patches may retain 10 to 95
percent of the initial total amount of
drug after the intended use period. This
raises a potential safety issue not only
to the patient, but also to others
including family members, caregivers,
children, and pets. For example, adverse
events due to a patient’s failure to
remove TDDS at the end of the intended
use period have been reported and are
generally related to an increased or
prolonged pharmacological effect of the
drug. Some children have died from
inadvertent exposure to discarded
TDDS. Reported adverse events
resulting from various quality problems
pertaining to TDDS have lead to product
recalls, withdrawals, and public health
advisories.
To reduce some of these risks, we
recommend that an enhanced design
and development approach—
specifically Quality by Design (QbD), as
described in the International
Conference on Harmonization (ICH)
guidance for industry Q8(R2)
Pharmaceutical Development—be used
when developing and manufacturing
TDDS, TMDS, and topical patches. We
also recommend that sufficient
scientific justification to support the
amount of residual drug in TDDS,
TMDS, or topical patches be included in
an application. The level of information
in the justification should be sufficient
to demonstrate product and process
understanding and ensure that a
scientific, risk-based approach has been
taken to minimize the amount of
residual drug in a system after use to the
lowest possible level. Furthermore, it is
expected that the amount of residual
drug in a newly developed system will
not exceed that of similar FDAapproved products.
This draft guidance is being issued
consistent with FDA’s good guidance
practices regulation (21 CFR 10.115).
The draft guidance, when finalized, will
represent the Agency’s current thinking
on residual drug in transdermal and
related drug delivery systems. It does
not create or confer any rights for or on
E:\FR\FM\03AUN1.SGM
03AUN1
Federal Register / Vol. 75, No. 148 / Tuesday, August 3, 2010 / Notices
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.
II. 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. Received
comments may be seen in the Division
of Dockets Management between 9 a.m.
and 4 p.m., Monday through Friday.
III. The 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). Information in
an application on the product and
process development and justification
for the final formulation and system
design is approved by OMB under
control numbers 0910–0001 and 0910–
0014.
IV. Electronic Access
Persons with access to the Internet
may obtain the document at either
https://www.fda.gov/Drugs/Guidance
ComplianceRegulatoryInformation/
Guidances/default.htm or https://
www.regulations.gov.
Dated: July 29, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–19041 Filed 8–2–10; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
erowe on DSK5CLS3C1PROD with NOTICES
[Docket No. FDA–2009–D–0181]
Guidance for Industry on Label
Comprehension Studies for
Nonprescription Drug Products;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing the
SUMMARY:
VerDate Mar<15>2010
14:41 Aug 02, 2010
Jkt 220001
availability of a guidance for industry
entitled ‘‘Label Comprehension Studies
for Nonprescription Drug Products.’’ The
guidance provides recommendations on
the design of label comprehension
studies that can be used to assess the
extent to which consumers understand
the information conveyed by proposed
nonprescription drug product labeling.
This guidance finalizes the draft
guidance published on May 1, 2009.
DATES: Submit either electronic or
written comments on agency guidances
at any time.
ADDRESSES: Submit written requests for
single copies of this guidance to the
Division of Drug Information, Center for
Drug Evaluation and Research, Food
and Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, rm. 2201,
Silver Spring, MD 20993–0002. Send
one self-addressed adhesive label to
assist that office in processing your
requests. See the SUPPLEMENTARY
INFORMATION section for electronic
access to the guidance document.
Submit electronic comments on the
guidance 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:
Murewa Oguntimein, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 22, rm.
5475,Silver Spring, MD 20993–0002,
301–796–4869.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is announcing the availability of
a guidance for industry entitled ‘‘Label
Comprehension Studies for
Nonprescription Drug Products.’’ This
guidance is intended for individuals or
organizations involved in the
development of label comprehension
studies for nonprescription drug
products. This guidance discusses
general concepts that should be
considered in the design and conduct of
a label comprehension study. This
guidance also incorporates advice
obtained from the September 25, 2006,
meeting of the Nonprescription Drug
Advisory Committee that considered
issues related to the analysis and
interpretation of consumer studies
conducted to support marketing of
nonprescription drug products, and
comments submitted to the draft
guidance published in the Federal
Register of May 1, 2009 (74 FR 20322).
This guidance is being issued
consistent with FDA’s good guidance
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
45641
practices regulation (21 CFR 10.115).
The guidance represents the agency’s
current thinking on label
comprehension studies for
nonprescription drug products. 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.
II. The Paperwork Reduction Act of
1995
This guidance refers to previously
approved collections of information that
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 parts 312 and
314 have been approved under OMB
control numbers 0910–0014 and 0910–
0001, respectively.
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. 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
Persons with access to the Internet
may obtain the document at either
https://www.fda.gov/Drugs/Guidance
ComplianceRegulatoryInformation/
Guidances/default.htm or https://
www.regulations.gov.
Dated: July 29, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–19043 Filed 8–2–10; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0363]
Medical Device User Fee Rates for
Fiscal Year 2011
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing the
SUMMARY:
E:\FR\FM\03AUN1.SGM
03AUN1
Agencies
[Federal Register Volume 75, Number 148 (Tuesday, August 3, 2010)]
[Notices]
[Pages 45640-45641]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-19041]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2010-D-0246]
Draft Guidance for Industry on Residual Drug in Transdermal and
Related Drug Delivery Systems; Availability
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing the
availability of a draft guidance for industry entitled ``Residual Drug
in Transdermal and Related Drug Delivery Systems.'' This draft guidance
provides recommendations to developers and manufacturers of transdermal
drug delivery systems (TDDS), transmucosal drug delivery systems
(TMDS), and topical patch products regarding use of an appropriate
scientific approach during product design and development--as well as
during manufacturing and product lifecycle management--to ensure that
the amount of residual drug substance at the end of the labeled use
period is minimized. The draft guidance is applicable to
investigational new drug applications (INDs), new drug applications
(NDAs), abbreviated new drug applications (ANDAs), and supplemental new
drug applications (sNDAs) for TDDS, TMDS, and topical patch products.
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 guidance before it begins work on the final version of the
guidance, submit either electronic or written comments on the draft
guidance, including comments regarding the proposed collection of
information, by November 1, 2010.
ADDRESSES: Submit written requests for single copies of the draft
guidance to the Division of Drug Information, Center for Drug
Evaluation and Research, Food and Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, rm. 2201, Silver Spring, MD 20993-0002. Send
one self-addressed adhesive label to assist that office in processing
your requests. See the SUPPLEMENTARY INFORMATION section for electronic
access to the draft guidance document.
Submit electronic comments on the draft guidance to https://www.regulations.gov. Submit written comments on the draft guidance to
the Division of Dockets Management (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Terrance Ocheltree, Center for Drug
Evaluation and Research, Food and Drug Administration, Bldg. 21, rm.
1609, 10903 New Hampshire Ave., Silver Spring, MD 20993-0002, 301-796-
1988.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is announcing the availability of a draft guidance for industry
entitled ``Residual Drug in Transdermal and Related Drug Delivery
Systems.'' This draft guidance provides recommendations to developers
and manufacturers of TDDS, TMDS, and topical patch products regarding
use of an appropriate scientific approach during product design and
development--as well as during manufacturing and product lifecycle
management--to ensure that the amount of residual drug substance at the
end of the labeled use period is minimized.
Existing TDDS, TMDS, and topical patches contain a larger amount of
the drug substance than what is intended to be delivered to the
patient. This excess amount of drug substance is needed to facilitate
delivery of the intended amount of the drug to the patient and remains
as residual drug in the used system. The amount of residual drug
substance in TDDS, TMDS, and topical patches has a significant
potential to impact the products' quality, safety, and efficacy.
Consequently, it is necessary to ensure that an appropriate scientific
approach is used to design and develop these products. The approach
should ensure that the amount of residual drug substance is minimized
consistent with the current state of technology.
Currently marketed TDDS, TMDS, and topical patches may retain 10 to
95 percent of the initial total amount of drug after the intended use
period. This raises a potential safety issue not only to the patient,
but also to others including family members, caregivers, children, and
pets. For example, adverse events due to a patient's failure to remove
TDDS at the end of the intended use period have been reported and are
generally related to an increased or prolonged pharmacological effect
of the drug. Some children have died from inadvertent exposure to
discarded TDDS. Reported adverse events resulting from various quality
problems pertaining to TDDS have lead to product recalls, withdrawals,
and public health advisories.
To reduce some of these risks, we recommend that an enhanced design
and development approach--specifically Quality by Design (QbD), as
described in the International Conference on Harmonization (ICH)
guidance for industry Q8(R2) Pharmaceutical Development--be used when
developing and manufacturing TDDS, TMDS, and topical patches. We also
recommend that sufficient scientific justification to support the
amount of residual drug in TDDS, TMDS, or topical patches be included
in an application. The level of information in the justification should
be sufficient to demonstrate product and process understanding and
ensure that a scientific, risk-based approach has been taken to
minimize the amount of residual drug in a system after use to the
lowest possible level. Furthermore, it is expected that the amount of
residual drug in a newly developed system will not exceed that of
similar FDA-approved products.
This draft guidance is being issued consistent with FDA's good
guidance practices regulation (21 CFR 10.115). The draft guidance, when
finalized, will represent the Agency's current thinking on residual
drug in transdermal and related drug delivery systems. It does not
create or confer any rights for or on
[[Page 45641]]
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.
II. 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. Received comments may be seen in the Division of Dockets
Management between 9 a.m. and 4 p.m., Monday through Friday.
III. The 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).
Information in an application on the product and process development
and justification for the final formulation and system design is
approved by OMB under control numbers 0910-0001 and 0910-0014.
IV. Electronic Access
Persons with access to the Internet may obtain the document at
either https://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm or https://www.regulations.gov.
Dated: July 29, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010-19041 Filed 8-2-10; 8:45 am]
BILLING CODE 4160-01-S