Announcement of Requirements and Registration for “Reporting Device Adverse Events Challenge”, 57045-57046 [2011-23702]
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wreier-aviles on DSKGBLS3C1PROD with NOTICES
Federal Register / Vol. 76, No. 179 / Thursday, September 15, 2011 / Notices
Eligibility Rules for Participating in
the Competition:
To be eligible to win a prize under
this challenge, an individual or entity:
(1) Shall have registered to participate
in the competition under the rules
promulgated by Office of the National
Coordinator for Health Information
Technology;
(2) Shall have complied with all the
requirements under this section;
(3) In the case of a private entity, shall
be incorporated in and maintain a
primary place of business in the United
States, and in the case of an individual,
whether participating singly or in a
group, shall be a citizen or permanent
resident of the United States; and
(4) May not be a Federal entity or
Federal employee acting within the
scope of their employment.
An individual or entity shall not be
deemed ineligible because the
individual or entity used Federal
facilities or consulted with Federal
employees during a competition if the
facilities and employees are made
available to all individuals and entities
participating in the competition on an
equitable basis.
Registered participants shall be
required to agree to assume any and all
risks and waive claims against the
Federal Government and its related
entities, except in the case of willful
misconduct, for any injury, death,
damage, or loss of property, revenue, or
profits, whether direct, indirect, or
consequential, arising from their
participation in a competition, whether
the injury, death, damage, or loss arises
through negligence or otherwise.
Participants shall be required to
obtain liability insurance or
demonstrate financial responsibility, in
amounts determined by the head of the
Office of the National Coordinator for
Health Information Technology, for
claims by—
(1) A third party for death, bodily
injury, or property damage, or loss
resulting from an activity carried out in
connection with participation in a
competition, with the Federal
Government named as an additional
insured under the registered
participant’s insurance policy and
registered participants agreeing to
indemnify the Federal Government
against third party claims for damages
arising from or related to competition
activities; and
(2) the Federal Government for
damage or loss to Government property
resulting from such an activity.
Participants must be teams of at least
two people.
VerDate Mar<15>2010
15:07 Sep 14, 2011
Jkt 223001
All participants are required to
provide written consent to the rules
upon or before submitting an entry.
Dates:
• Submission Period Begins: 12:01
a.m., E.D.T., September 12, 2011.
• Submission Period Ends: 11:59
p.m., E.D.T., November 16, 2011.
Registration Process for Participants:
To register for this challenge
participants should:
• Access the https://
www.challenge.gov Web site and search
for the ‘‘Ensuring Safe Transitions from
Hospital to Home’’.
• Access the ONC Investing in
Innovation (i2) Challenge Web site at:
Æ https://www.health2challenge.org/
category/onc/
Æ A registration link for the challenge
can be found on the landing page under
the challenge description.
Amount of the Prize:
• First Prize: $25,000.
• Second Prize: $10,000.
• Third Prize: $5,000.
Awards may be subject to Federal
income taxes and HHS will comply with
IRS withholding and reporting
requirements, where applicable.
Basis Upon Which Winner Will Be
Selected:
The judging panel will make
selections based upon the following
criteria:
1. Innovation.
2. Usability/Design.
3. Potential for impact.
4. Data integration.
5. Use of NwHIN standards and
services.
Additional Information:
Ownership of intellectual property is
determined by the following:
• Each entrant retains title and full
ownership in and to their submission.
Entrants expressly reserve all
intellectual property rights not
expressly granted under the challenge
agreement.
• By participating in the challenge,
each entrant hereby irrevocably grants
to Sponsor and Administrator a limited,
non-exclusive, royalty free, worldwide,
license and right to reproduce,
publically perform, publically display,
and use the Submission to the extent
necessary to administer the challenge,
and to publically perform and
publically display the Submission,
including, without limitation, for
advertising and promotional purposes
relating to the challenge.
Dated: September 8, 2011.
Farzad Mostashari,
National Coordinator for Health Information
Technology.
[FR Doc. 2011–23704 Filed 9–14–11; 8:45 am]
BILLING CODE 4150–45–P
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57045
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Announcement of Requirements and
Registration for ‘‘Reporting Device
Adverse Events Challenge’’
Authority: 15 U.S.C. 3719.
Office of the National
Coordinator for Health Information
Technology, HHS.
ACTION: Notice.
AGENCY:
Medical devices will play an
increasingly large role in the monitoring
and collection of patient data with the
spread of electronic health records. The
United States has a limited system for
the post-market surveillance of medical
devices, specifically as it relates to
monitoring product safety and
effectiveness. The ‘‘Reporting Device
Adverse Events Challenge’’ asks multidisciplinary teams to develop an
application that facilitates the reporting
of adverse events related to medical
devices, whether implanted or used in
the hospital, clinic, or home.
The statutory authority for this
challenge competition is Section 105 of
the America COMPETES
Reauthorization Act of 2010 (Pub. L.
111–358).
DATES: Effective on September 12, 2011.
FOR FURTHER INFORMATION CONTACT:
Adam Wong, 202–720–2866.
Wil Yu, 202–690–5920.
SUPPLEMENTARY INFORMATION:
Subject of Challenge Competition:
The ‘‘Reporting Device Adverse Events
Challenge’’ asks multi-disciplinary
teams to develop an application that
facilitates the reporting of adverse
events related to medical devices,
whether implanted or used in the
hospital, clinic, or home. The
application would make it easy for
patients to report adverse events to their
provider, support the download of
information from EMR or PHR systems
to populate the adverse event report and
provide high quality data, capture
useful information including patient
demographics and device data that is
easily accessible to all stakeholders
(patients, providers, manufacturers, and
researchers) using current technologies
including PC-based browsers, mobile
phones, and tablets, and leverage
NwHIN standards and services
including transport, content, and
vocabularies.
Eligibility Rules for Participating in
the Competition:
To be eligible to win a prize under
this challenge, an individual or entity:
(1) Shall have registered to participate
in the competition under the rules
SUMMARY:
E:\FR\FM\15SEN1.SGM
15SEN1
wreier-aviles on DSKGBLS3C1PROD with NOTICES
57046
Federal Register / Vol. 76, No. 179 / Thursday, September 15, 2011 / Notices
promulgated by Office of the National
Coordinator for Health Information
Technology;
(2) Shall have complied with all the
requirements under this section;
(3) In the case of a private entity, shall
be incorporated in and maintain a
primary place of business in the United
States, and in the case of an individual,
whether participating singly or in a
group, shall be a citizen or permanent
resident of the United States; and
(4) May not be a Federal entity or
Federal employee acting within the
scope of their employment.
An individual or entity shall not be
deemed ineligible because the
individual or entity used Federal
facilities or consulted with Federal
employees during a competition if the
facilities and employees are made
available to all individuals and entities
participating in the competition on an
equitable basis.
Registered participants shall be
required to agree to assume any and all
risks and waive claims against the
Federal Government and its related
entities, except in the case of willful
misconduct, for any injury, death,
damage, or loss of property, revenue, or
profits, whether direct, indirect, or
consequential, arising from their
participation in a competition, whether
the injury, death, damage, or loss arises
through negligence or otherwise.
Participants shall be required to
obtain liability insurance or
demonstrate financial responsibility, in
amounts determined by the head of the
Office of the National Coordinator for
Health Information Technology, for
claims by—
(1) A third party for death, bodily
injury, or property damage, or loss
resulting from an activity carried out in
connection with participation in a
competition, with the Federal
Government named as an additional
insured under the registered
participant’s insurance policy and
registered participants agreeing to
indemnify the Federal Government
against third party claims for damages
arising from or related to competition
activities; and
(2) the Federal Government for
damage or loss to Government property
resulting from such an activity.
Participants must be teams of at least
two people.
All participants are required to
provide written consent to the rules
upon or before submitting an entry.
Dates:
• Submission Period Begins: 12:01
a.m., E.D.T., September 12, 2011.
• Submission Period Ends: 11:59
p.m., E.D.T., December 2, 2011.
VerDate Mar<15>2010
15:07 Sep 14, 2011
Jkt 223001
Registration Process for Participants:
To register for this challenge
participants should:
• Access the https://
www.challenge.gov Web site and search
for the ‘‘Reporting Device Adverse
Events Challenge’’.
• Access the ONC Investing in
Innovation (i2) Challenge Web site at:
Æ https://www.health2challenge.org/
category/onc/.
Æ A registration link for the challenge
can be found on the landing page under
the challenge description.
Amount of the Prize:
• First Prize: $25,000.
• Second Prize: $10,000.
• Third Prize: $5,000.
Awards may be subject to Federal
income taxes and HHS will comply with
IRS withholding and reporting
requirements, where applicable.
Basis Upon Which Winner Will Be
Selected:
The judging panel will make
selections based upon the following
criteria:
1. Effectiveness in facilitating adverse
event reporting.
2. Usability and design.
3. Ability to integrate with electronic
health records and other data sources.
4. Creativity and Innovation.
5. Use of NwHIN standards and
services.
Additional Information:
Ownership of intellectual property is
determined by the following:
• Each entrant retains title and full
ownership in and to their submission.
Entrants expressly reserve all
intellectual property rights not
expressly granted under the challenge
agreement.
• By participating in the challenge,
each entrant hereby irrevocably grants
to Sponsor and Administrator a limited,
non-exclusive, royalty free, worldwide,
license and right to reproduce,
publically perform, publically display,
and use the Submission to the extent
necessary to administer the challenge,
and to publically perform and
publically display the Submission,
including, without limitation, for
advertising and promotional purposes
relating to the challenge.
Dated: September 8, 2011.
Farzad Mostashari,
National Coordinator for Health Information
Technology.
[FR Doc. 2011–23702 Filed 9–14–11; 8:45 am]
BILLING CODE 4150–45–P
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Frm 00030
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
AGENCY:
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve the proposed
information collection project: ‘‘Health
Literacy Item Set Supplemental to
CAHPS Health Plan Survey—Pretest of
Proposed Questions and Methodology.’’
In accordance with the Paperwork
Reduction Act, 44 U.S.C. 3501–3521,
AHRQ invites the public to comment on
this proposed information collection.
This proposed information collection
was previously published in the Federal
Register on July 7th, 2011 and allowed
60 days for public comment. No
comments were received. The purpose
of this notice is to allow an additional
30 days for public comment.
DATES: Comments on this notice must be
received by October 17, 2011.
ADDRESSES: Written comments should
be submitted to: AHRQ’s OMB Desk
Officer by fax at (202) 395–6974
(attention: AHRQ’s desk officer) or by email at OIRA_submission@omb.eop.gov
(attention: AHRQ’s desk officer).
Copies of the proposed collection
plans, data collection instruments, and
specific details on the estimated burden
can be obtained from the AHRQ Reports
Clearance Officer.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
e-mail at
doris.lefkowitz@AHRQ.hhs.gov.
SUMMARY:
SUPPLEMENTARY INFORMATION:
Proposed Project
Health Literacy Item Set Supplemental
to CAHPS Health Plan Survey—Pretest
of Proposed Questions and Methodology
The Consumer Assessment of
Healthcare Providers and Systems
(CAHPS®) program is a multi-year
initiative. AHRQ first launched the
program in October 1995 in response to
concerns about the lack of good
information about the quality of health
plans from the enrollees’ perspective.
Numerous public and private
organizations collected information on
E:\FR\FM\15SEN1.SGM
15SEN1
Agencies
[Federal Register Volume 76, Number 179 (Thursday, September 15, 2011)]
[Notices]
[Pages 57045-57046]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-23702]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Announcement of Requirements and Registration for ``Reporting
Device Adverse Events Challenge''
Authority: 15 U.S.C. 3719.
AGENCY: Office of the National Coordinator for Health Information
Technology, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Medical devices will play an increasingly large role in the
monitoring and collection of patient data with the spread of electronic
health records. The United States has a limited system for the post-
market surveillance of medical devices, specifically as it relates to
monitoring product safety and effectiveness. The ``Reporting Device
Adverse Events Challenge'' asks multi-disciplinary teams to develop an
application that facilitates the reporting of adverse events related to
medical devices, whether implanted or used in the hospital, clinic, or
home.
The statutory authority for this challenge competition is Section
105 of the America COMPETES Reauthorization Act of 2010 (Pub. L. 111-
358).
DATES: Effective on September 12, 2011.
FOR FURTHER INFORMATION CONTACT:
Adam Wong, 202-720-2866.
Wil Yu, 202-690-5920.
SUPPLEMENTARY INFORMATION:
Subject of Challenge Competition: The ``Reporting Device Adverse
Events Challenge'' asks multi-disciplinary teams to develop an
application that facilitates the reporting of adverse events related to
medical devices, whether implanted or used in the hospital, clinic, or
home. The application would make it easy for patients to report adverse
events to their provider, support the download of information from EMR
or PHR systems to populate the adverse event report and provide high
quality data, capture useful information including patient demographics
and device data that is easily accessible to all stakeholders
(patients, providers, manufacturers, and researchers) using current
technologies including PC-based browsers, mobile phones, and tablets,
and leverage NwHIN standards and services including transport, content,
and vocabularies.
Eligibility Rules for Participating in the Competition:
To be eligible to win a prize under this challenge, an individual
or entity:
(1) Shall have registered to participate in the competition under
the rules
[[Page 57046]]
promulgated by Office of the National Coordinator for Health
Information Technology;
(2) Shall have complied with all the requirements under this
section;
(3) In the case of a private entity, shall be incorporated in and
maintain a primary place of business in the United States, and in the
case of an individual, whether participating singly or in a group,
shall be a citizen or permanent resident of the United States; and
(4) May not be a Federal entity or Federal employee acting within
the scope of their employment.
An individual or entity shall not be deemed ineligible because the
individual or entity used Federal facilities or consulted with Federal
employees during a competition if the facilities and employees are made
available to all individuals and entities participating in the
competition on an equitable basis.
Registered participants shall be required to agree to assume any
and all risks and waive claims against the Federal Government and its
related entities, except in the case of willful misconduct, for any
injury, death, damage, or loss of property, revenue, or profits,
whether direct, indirect, or consequential, arising from their
participation in a competition, whether the injury, death, damage, or
loss arises through negligence or otherwise.
Participants shall be required to obtain liability insurance or
demonstrate financial responsibility, in amounts determined by the head
of the Office of the National Coordinator for Health Information
Technology, for claims by--
(1) A third party for death, bodily injury, or property damage, or
loss resulting from an activity carried out in connection with
participation in a competition, with the Federal Government named as an
additional insured under the registered participant's insurance policy
and registered participants agreeing to indemnify the Federal
Government against third party claims for damages arising from or
related to competition activities; and
(2) the Federal Government for damage or loss to Government
property resulting from such an activity.
Participants must be teams of at least two people.
All participants are required to provide written consent to the
rules upon or before submitting an entry.
Dates:
Submission Period Begins: 12:01 a.m., E.D.T., September
12, 2011.
Submission Period Ends: 11:59 p.m., E.D.T., December 2,
2011.
Registration Process for Participants:
To register for this challenge participants should:
Access the https://www.challenge.gov Web site and search
for the ``Reporting Device Adverse Events Challenge''.
Access the ONC Investing in Innovation (i2) Challenge Web
site at:
[cir] https://www.health2challenge.org/category/onc/.
[cir] A registration link for the challenge can be found on the
landing page under the challenge description.
Amount of the Prize:
First Prize: $25,000.
Second Prize: $10,000.
Third Prize: $5,000.
Awards may be subject to Federal income taxes and HHS will comply
with IRS withholding and reporting requirements, where applicable.
Basis Upon Which Winner Will Be Selected:
The judging panel will make selections based upon the following
criteria:
1. Effectiveness in facilitating adverse event reporting.
2. Usability and design.
3. Ability to integrate with electronic health records and other
data sources.
4. Creativity and Innovation.
5. Use of NwHIN standards and services.
Additional Information:
Ownership of intellectual property is determined by the following:
Each entrant retains title and full ownership in and to
their submission. Entrants expressly reserve all intellectual property
rights not expressly granted under the challenge agreement.
By participating in the challenge, each entrant hereby
irrevocably grants to Sponsor and Administrator a limited, non-
exclusive, royalty free, worldwide, license and right to reproduce,
publically perform, publically display, and use the Submission to the
extent necessary to administer the challenge, and to publically perform
and publically display the Submission, including, without limitation,
for advertising and promotional purposes relating to the challenge.
Dated: September 8, 2011.
Farzad Mostashari,
National Coordinator for Health Information Technology.
[FR Doc. 2011-23702 Filed 9-14-11; 8:45 am]
BILLING CODE 4150-45-P