Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Experimental Evaluation of Variations in Content and Format of the Brief Summary in Direct-to-Consumer Print Advertisements for Prescription Drugs, 59536 [E7-20756]
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59536
Federal Register / Vol. 72, No. 203 / Monday, October 22, 2007 / Notices
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents. Consideration will be
given to comments and suggestions
submitted within 60 days of this
publication.
the Internet at https://www.fda.gov/
ohrms/dockets.
Dated: October 12, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7–20756 Filed 10–19–07; 8:45 am]
BILLING CODE 4160–01–S
Dated: October 10, 2007.
Brendan C. Kelly,
Reports Clearance Officer.
[FR Doc. 07–5176 Filed 10–19–07; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 4184–01–M
[Docket No. 2007N–0114]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Electronic Distribution of Prescribing
Information for Prescription Drug
Products; Reopening of Comment
Period
Food and Drug Administration
Food and Drug Administration
AGENCY:
ACTION:
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Experimental Evaluation of Variations
in Content and Format of the Brief
Summary in Direct-to-Consumer Print
Advertisements for Prescription Drugs
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Experimental Evaluation of Variations
in Content and Format of the Brief
Summary in Direct-to-Consumer (DTC)
Print Advertisements for Prescription
Drugs’’ has been approved by the Office
of Management and Budget (OMB)
under the Paperwork Reduction Act of
1995.
FOR FURTHER INFORMATION CONTACT:
Karen L. Nelson, Office of the Chief
Information Officer (HFA–250), Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301–827–
4816.
In the
Federal Register of March 14, 2007 (72
FR 11889), the agency announced that
the proposed information collection had
been submitted to OMB for review and
clearance under 44 U.S.C. 3507. An
agency may not conduct or sponsor, and
a person is not required to respond to,
a collection of information unless it
displays a currently valid OMB control
number. OMB has now approved the
information collection and has assigned
OMB control number 0910–0611. The
approval expires on October 31, 2010. A
copy of the supporting statement for this
information collection is available on
ebenthall on PRODPC61 with NOTICES
SUPPLEMENTARY INFORMATION:
VerDate Aug<31>2005
15:02 Oct 19, 2007
Food and Drug Administration,
HHS.
[Docket No. 2006N–0133]
Jkt 214001
Notice; reopening of comment
period.
SUMMARY: The Food and Drug
Administration (FDA) is reopening to
December 6, 2007 the comment period
for the notice that published in the
Federal Register of April 2, 2007 (72 FR
15701); this notice was related to the
public hearing of April 27, 2007,
concerning the electronic distribution of
FDA-approved prescribing information
currently contained in the package
insert (PI) for prescription drug and
biological products. FDA is reopening
the comment period for the sole purpose
of inviting interested persons to submit
comments on the concept of electronic
distribution of FDA-approved
prescribing information currently
contained in the PI for prescription
animal drug products.
DATES: Submit written or electronic
comments by December 6, 2007.
ADDRESSES: Submit written comments
to the Division of Dockets Management
(HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. Submit
electronic comments to either https://
www.fda.gov/dockets/ecomments or
https://www.regulations.gov.
FOR FURTHER INFORMATION CONTACT: Erik
Mettler, Office of Policy (HF–11), Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301–827–
3360, Erik.Mettler@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register notice of April
2, 2007 (72 FR 15701), FDA published
a notice of public hearing concerning
the concept of the electronic
distribution of PIs for human
prescription drugs and biological
PO 00000
Frm 00026
Fmt 4703
Sfmt 4703
products and solicited relevant
information and comments on this
concept. The purpose was to garner
views and information on the feasibility
of establishing an efficient process for
industry to electronically distribute
prescribing information to dispensers.
The PIs with prescribing information
accompany prescription human drugs to
meet the requirement that ‘‘labeling on
or within the package from which the
drug is to be dispensed bears adequate
information for its use * * *’’ (21 CFR
201.100(c)(1)). For additional
information, see the April 2, 2007,
notice ( 72 FR 15701).
Currently, the PI contains the
prescribing information for the safe and
effective use of the product in the form
of a paper leaflet. Although the
information in the PI is a valuable
resource, it is often not readily
accessible when a healthcare provider
who has not physically received the
drug makes a treatment decision or
discusses treatments with a patient.
Additionally, the PI may not contain the
most current information, because the PI
accompanying the drug’s distribution
may have been printed and distributed
prior to more recent labeling changes.
Accordingly, with technological
advances in the electronic transmission
of information, we are considering how
prescribing information could be more
effectively disseminated.
FDA is reopening the comment period
for the sole purpose of inviting
interested persons to submit comments
addressing a number of questions
regarding the current use of package
inserts for animal drug products and
those logistical issues associated with
electronic distribution of such
prescribing information for animal drug
products. The previous request for
comments was limited to human drugs
and biologics. As with prescription
human drugs, the PIs with prescribing
information accompany prescription
animal drugs to meet the requirement
that ‘‘labeling on or within the package
from which the drug is to be dispensed
bears adequate information for its use
* * *’’ (21 CFR 201.105(c)(1)). FDA
approves the prescribing information as
part of both human and animal drug
labeling in the drug application. The
request for comment is to gain a better
understanding of how PIs for animal
drugs are currently used by healthcare
entities as we consider new approaches
for the dissemination of labeling
information.
II. Issues for Discussion
FDA is specifically interested in
receiving comments on the following
questions and any other pertinent
E:\FR\FM\22OCN1.SGM
22OCN1
]]>Agencies
[Federal Register Volume 72, Number 203 (Monday, October 22, 2007)]
[Notices]
[Page 59536]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-20756]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 2006N-0133]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approval; Experimental Evaluation of
Variations in Content and Format of the Brief Summary in Direct-to-
Consumer Print Advertisements for Prescription Drugs
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that a
collection of information entitled ``Experimental Evaluation of
Variations in Content and Format of the Brief Summary in Direct-to-
Consumer (DTC) Print Advertisements for Prescription Drugs'' has been
approved by the Office of Management and Budget (OMB) under the
Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT: Karen L. Nelson, Office of the Chief
Information Officer (HFA-250), Food and Drug Administration, 5600
Fishers Lane, Rockville, MD 20857, 301-827-4816.
SUPPLEMENTARY INFORMATION: In the Federal Register of March 14, 2007
(72 FR 11889), the agency announced that the proposed information
collection had been submitted to OMB for review and clearance under 44
U.S.C. 3507. An agency may not conduct or sponsor, and a person is not
required to respond to, a collection of information unless it displays
a currently valid OMB control number. OMB has now approved the
information collection and has assigned OMB control number 0910-0611.
The approval expires on October 31, 2010. A copy of the supporting
statement for this information collection is available on the Internet
at https://www.fda.gov/ohrms/dockets.
Dated: October 12, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7-20756 Filed 10-19-07; 8:45 am]
BILLING CODE 4160-01-S
