Office for Civil Rights; Workshop on the HIPAA Privacy Rule's De-Identification Standard; Notice of Meeting, 8363-8364 [2010-3663]
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Federal Register / Vol. 75, No. 36 / Wednesday, February 24, 2010 / Notices
comments was published in the Federal
Register at 74 FR 65535, on December
10, 2009. No public comments were
received.
Public comments are particularly
invited on: Whether this collection of
information is necessary for the proper
performance of functions of the FAR,
and whether it will have practical
utility; whether our estimate of the
public burden of this collection of
information is accurate, and based on
valid assumptions and methodology;
ways to enhance the quality, utility, and
clarity of the information to be
collected; and ways in which we can
minimize the burden of the collection of
information on those who are to
respond, through the use of appropriate
technological collection techniques or
other forms of information technology.
DATES: Submit comments on or before
March 26, 2010.
ADDRESSES: Submit comments including
suggestions for reducing this burden to:
FAR Desk Officer, OMB, Room 10102,
NEOB, Washington, DC 20503, and a
copy to the General Services
Administration, Regulatory Secretariat
(MVCB), 1800 F Street, NW., Room
4041, Washington, DC 20405.
FOR FURTHER INFORMATION CONTACT:
Ernest Woodson, Contract Policy
Division, GSA (202) 501–3775 or e-mail
ernest.woodson@gsa.gov.
SUPPLEMENTARY INFORMATION:
A. Purpose
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The patent coverage in FAR subpart
27.2 requires the contractor to report
each notice of a claim of patent or
copyright infringement that came to the
contractor’s attention in connection
with performing a Government contract
(sections 27.202–1 and 52.227–2). The
contractor is also required to report all
royalties anticipated or paid in excess of
$250 for the use of patented inventions
by furnishing the name and address of
licensor; date of license agreement;
patent application serial number, or
other basis on which the royalty is
payable; brief description of item or
component, percentage or dollar rate of
royalty per unit, unit price of contract
item, and number of units (sections
27.204–1, 52.227–6, and 52.227–9). The
information collected is to protect the
rights of the patent holder and the
interest of the Government.
B. Annual Reporting Burden
Number of Respondents: 30.
Responses per Respondent: 1.
Total Responses: 30.
Average Burden Hours per Response:
.5.
Total Burden Hours: 15.
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16:49 Feb 23, 2010
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Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat (MVCB), 1800 F
Street, NW., Room 4041, Washington,
DC 20405, telephone (202) 501–4755.
Please cite OMB Control No. 9000–0096,
Patents, in all correspondence.
Dated: February 18, 2010.
Al Matera,
Director, Acquisition Policy Division.
[FR Doc. 2010–3686 Filed 2–23–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the National Biodefense
Science Board
AGENCY: Department of Health and
Human Services, Office of the Secretary.
ACTION: Notice.
As stipulated by the Federal
Advisory Committee Act, the U.S.
Department of Health and Human
Services is hereby giving notice that the
National Biodefense Science Board
(NBSB) will be holding a public
meeting. The meeting is open to the
public.
SUMMARY:
DATES: The NBSB will hold a public
meeting on March 26, 2010 from 8 a.m.
to 5 p.m. ET. The agenda is subject to
change as priorities dictate.
ADDRESSES: Washington, DC Metro
Area. The venue details will be posted
on the NBSB Web page at https://
www.hhs.gov/aspr/omsph/nbsb/
index.html as they become available.
FOR FURTHER INFORMATION CONTACT: Email: NBSB@HHS.GOV.
SUPPLEMENTARY INFORMATION: Pursuant
to section 319M of the Public Health
Service Act (42 U.S.C. 247d–7f) and
section 222 of the Public Health Service
Act (42 U.S.C. 217a), the Department of
Health and Human Services established
the National Biodefense Science Board.
The Board shall provide expert advice
and guidance to the Secretary on
scientific, technical, and other matters
of special interest to the Department of
Health and Human Services regarding
current and future chemical, biological,
nuclear, and radiological agents,
whether naturally occurring, accidental,
or deliberate. The Board may also
provide advice and guidance to the
Secretary on other matters related to
public health emergency preparedness
and response.
Background: The Board will discuss
and consider recommendations from the
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8363
National Biodefense Science Board’s
Medical Countermeasure Enterprise
Working Group report regarding the
issues and challenges facing the Public
Health Emergency Medical
Countermeasure Enterprise (PHEMCE).
Availability of Materials: The meeting
agenda and other materials will be
posted on the NBSB Web site at
https://www.hhs.gov/aspr/omsph/nbsb/
index.html prior to the meeting.
Procedures for Providing Public Input:
Any member of the public providing
oral comments at the meeting must signin at the registration desk and provide
his/her name, address, and affiliation.
All written comments must be received
prior to March 25, 2010, and should be
sent by e-mail to NBSB@HHS.GOV with
‘‘NBSB Public Comment’’ as the subject
line. Individuals who plan to attend and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should email NBSB@HHS.GOV.
Dated: February 18, 2010.
Nicole Lurie,
Assistant Secretary for Preparedness and
Response.
[FR Doc. 2010–3670 Filed 2–23–10; 8:45 am]
BILLING CODE 4150–37–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office for Civil Rights; Workshop on
the HIPAA Privacy Rule’s DeIdentification Standard; Notice of
Meeting
Office for Civil Rights, HHS.
Notice of meeting.
AGENCY:
ACTION:
This notice announces a forthcoming
workshop organized by the Office for
Civil Rights (OCR). The meeting will be
open to the public.
General Purpose of the Meeting:
Section 13424 (c) of the Health
Information Technology for Clinical and
Economic Health (HITECH) Act, part of
the American Recovery and
Reinvestment Act of 2009 (ARRA),1
requires HHS to issue guidance on
methods for de-identification of
protected health information as
designated in the Health Insurance
Portability and Accountability Act
(HIPAA) Privacy Rule. In response to
this mandate, OCR is soliciting
stakeholder input from experts with
practical technical and policy
experience to inform the creation of
guidance materials. OCR is collecting
views regarding de-identification
approaches, best practices for
1 Public
E:\FR\FM\24FEN1.SGM
Law 111–5.
24FEN1
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8364
Federal Register / Vol. 75, No. 36 / Wednesday, February 24, 2010 / Notices
implementation and management of the
current de-identification standard and
potential changes to address policy
concerns.
To facilitate timely collection of
information, OCR is organizing an inperson two (2)-day workshop that will
consist of multiple panels. Each panel
will address a specific topic related to
the Privacy Rule’s de-identification
methodologies and policies. The
workshop will be open to the public and
each panel presentation will be
followed by a question-answer period.
At the present time, this is the only
workshop planned.
DATE AND TIME: The meeting will be held
on March 8, 2010, from 8 a.m. to 5:15
p.m./Eastern Time and March 9, 2010
from 8:30 a.m. to 11:30 a.m.
LOCATION: Washington Marriott at Metro
Center, 775 12th Street NW.,
Washington, District of Columbia 20005.
The hotel telephone number is 202–
737–2200.
CONTACT PERSON: Andra Wicks, Office
for Civil Rights, HHS, 200 Independence
Ave, SW., Washington, DC 20201, 202–
205–2292, Fax: 202–205–4786, e-mail:
andra.wicks@hhs.gov. Please call the
contact person for information on this
meeting, view workshop updates on our
Web site at https://www.hhs.gov/ocr/
privacy, or register for the workshop at
https://www.fedmeetings.net/common/
registration.cfm?mid=2852.
Agenda: The two (2)-day workshop
will explore the following topics related
to the de-identification of protected
health information standard 2:
—Methodological Issues Associated
with HIPAA Privacy Rule DeIdentification.
—Statistical Disclosure Control and
HIPAA Privacy Rule Protections.
—Anonymization and the HIPAA
Privacy Rule.
—Policy Interpretations of HIPAA
Privacy Rule De-Identification
Requirements.
—De-Identification and Legal Contracts.
Each ninety (90) minute panel will
include presentations by industry
experts followed by a discussion period.
The discussion will include questions
posed by workshop participants and the
general public attending the meeting inperson and via Web cast.
OCR intends to make background
material available to the public no later
than two (2) business days prior to the
meeting. If OCR is unable to post the
background material on its Web site
prior to the meeting, it will be made
publicly available at the location of the
workshop, and the background material
2 45
CFR 164.514(b).
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16:49 Feb 23, 2010
Jkt 220001
will be posted on OCR’s Web site after
the meeting, at https://www.hhs.gov/ocr/
privacy.
Procedure: Interested persons may
present data, information, or views,
orally or in writing, on issues pending
before the workshop. Written
submissions may be made to
OCRPrivacy@hhs.gov, with the
workshop title ‘‘Workshop on the
HIPAA Privacy Rule’s De-Identification
Standard’’ in the subject line on or
before Friday, March 5, 2010.
Oral comments from the public will
be permitted after each panel. Time
allotted for each presentation is limited
to three minutes. If the number of
speakers requesting to comment is
greater than can be reasonably
accommodated during the scheduled
open public hearing session, OCR will
take written comments after the meeting
until Friday, March 12, 2010.
After the workshop, OCR will
synthesize the input from workshop
panelists and general comments to
incorporate into guidance. The guidance
will be posted on the OCR Web site for
public comment. OCR may provide
revised guidance incorporating the
public comment.
OCR welcomes the attendance of the
public at this workshop. Seating is
limited at the location, and OCR will
make every effort to accommodate
persons with physical disabilities or
special needs. If you require special
accommodations due to a disability,
please contact Andra Wicks at least
seven (7) days in advance of the
meeting.
Dated: February 17, 2010.
Zinethia L. Clemmons,
Health Information Privacy Specialist, Office
for Civil Rights, Health Information Privacy
Division.
[FR Doc. 2010–3663 Filed 2–23–10; 8:45 am]
BILLING CODE 4153–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day-10–0215]
Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
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request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–5960 or send
comments to Maryam I. Daneshvar, CDC
Acting Reports Clearance Officer, 1600
Clifton Road, MS–D74, Atlanta, GA
30333 or send an e-mail to
omb@cdc.gov.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance 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, including through the
use of automated collection techniques
or other forms of information
technology. Written comments should
be received within 60 days of this
notice.
Proposed Project
National Death Index (NDI), (OMB
No. 0920–0215)—Extension—National
Center for Health Statistics (NCHS),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C. 242k), as
amended, authorizes that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, shall collect
statistics on the extent and nature of
illness and disability of the population
of the United States.
The National Death Index (NDI) is a
national data base containing
identifying death record information
submitted annually to NCHS by all the
State vital statistics offices, beginning
with deaths in 1979. Searches against
the NDI file provide the states and dates
of death, and the death certificate
numbers of deceased study subjects.
Using the NDI Plus service,
researchers have the option of also
receiving cause of death information for
deceased subjects, thus reducing the
need to request copies of death
certificates from the States. The NDI
Plus option currently provides the ICD
codes for the underlying and multiple
causes of death for the years 1979–2007.
Health researchers must complete five
administrative forms in order to apply
for NDI services, and submit records of
study subjects for computer matching
against the NDI file. A three-year
clearance is requested. There is no cost
to respondents except for their time.
E:\FR\FM\24FEN1.SGM
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Agencies
[Federal Register Volume 75, Number 36 (Wednesday, February 24, 2010)]
[Notices]
[Pages 8363-8364]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-3663]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office for Civil Rights; Workshop on the HIPAA Privacy Rule's De-
Identification Standard; Notice of Meeting
AGENCY: Office for Civil Rights, HHS.
ACTION: Notice of meeting.
-----------------------------------------------------------------------
This notice announces a forthcoming workshop organized by the
Office for Civil Rights (OCR). The meeting will be open to the public.
General Purpose of the Meeting: Section 13424 (c) of the Health
Information Technology for Clinical and Economic Health (HITECH) Act,
part of the American Recovery and Reinvestment Act of 2009 (ARRA),\1\
requires HHS to issue guidance on methods for de-identification of
protected health information as designated in the Health Insurance
Portability and Accountability Act (HIPAA) Privacy Rule. In response to
this mandate, OCR is soliciting stakeholder input from experts with
practical technical and policy experience to inform the creation of
guidance materials. OCR is collecting views regarding de-identification
approaches, best practices for
[[Page 8364]]
implementation and management of the current de-identification standard
and potential changes to address policy concerns.
---------------------------------------------------------------------------
\1\ Public Law 111-5.
---------------------------------------------------------------------------
To facilitate timely collection of information, OCR is organizing
an in-person two (2)-day workshop that will consist of multiple panels.
Each panel will address a specific topic related to the Privacy Rule's
de-identification methodologies and policies. The workshop will be open
to the public and each panel presentation will be followed by a
question-answer period. At the present time, this is the only workshop
planned.
Date and Time: The meeting will be held on March 8, 2010, from 8 a.m.
to 5:15 p.m./Eastern Time and March 9, 2010 from 8:30 a.m. to 11:30
a.m.
Location: Washington Marriott at Metro Center, 775 12th Street NW.,
Washington, District of Columbia 20005. The hotel telephone number is
202-737-2200.
Contact Person: Andra Wicks, Office for Civil Rights, HHS, 200
Independence Ave, SW., Washington, DC 20201, 202-205-2292, Fax: 202-
205-4786, e-mail: andra.wicks@hhs.gov. Please call the contact person
for information on this meeting, view workshop updates on our Web site
at https://www.hhs.gov/ocr/privacy, or register for the workshop at
https://www.fedmeetings.net/common/registration.cfm?mid=2852.
Agenda: The two (2)-day workshop will explore the following topics
related to the de-identification of protected health information
standard \2\:
---------------------------------------------------------------------------
\2\ 45 CFR 164.514(b).
--Methodological Issues Associated with HIPAA Privacy Rule De-
Identification.
--Statistical Disclosure Control and HIPAA Privacy Rule Protections.
--Anonymization and the HIPAA Privacy Rule.
--Policy Interpretations of HIPAA Privacy Rule De-Identification
Requirements.
--De-Identification and Legal Contracts.
Each ninety (90) minute panel will include presentations by
industry experts followed by a discussion period. The discussion will
include questions posed by workshop participants and the general public
attending the meeting in-person and via Web cast.
OCR intends to make background material available to the public no
later than two (2) business days prior to the meeting. If OCR is unable
to post the background material on its Web site prior to the meeting,
it will be made publicly available at the location of the workshop, and
the background material will be posted on OCR's Web site after the
meeting, at https://www.hhs.gov/ocr/privacy.
Procedure: Interested persons may present data, information, or
views, orally or in writing, on issues pending before the workshop.
Written submissions may be made to OCRPrivacy@hhs.gov, with the
workshop title ``Workshop on the HIPAA Privacy Rule's De-Identification
Standard'' in the subject line on or before Friday, March 5, 2010.
Oral comments from the public will be permitted after each panel.
Time allotted for each presentation is limited to three minutes. If the
number of speakers requesting to comment is greater than can be
reasonably accommodated during the scheduled open public hearing
session, OCR will take written comments after the meeting until Friday,
March 12, 2010.
After the workshop, OCR will synthesize the input from workshop
panelists and general comments to incorporate into guidance. The
guidance will be posted on the OCR Web site for public comment. OCR may
provide revised guidance incorporating the public comment.
OCR welcomes the attendance of the public at this workshop. Seating
is limited at the location, and OCR will make every effort to
accommodate persons with physical disabilities or special needs. If you
require special accommodations due to a disability, please contact
Andra Wicks at least seven (7) days in advance of the meeting.
Dated: February 17, 2010.
Zinethia L. Clemmons,
Health Information Privacy Specialist, Office for Civil Rights, Health
Information Privacy Division.
[FR Doc. 2010-3663 Filed 2-23-10; 8:45 am]
BILLING CODE 4153-01-P