USPTO Cancer Moonshot Challenge, 61196-61198 [2016-21349]
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mstockstill on DSK3G9T082PROD with NOTICES
61196
Federal Register / Vol. 81, No. 172 / Tuesday, September 6, 2016 / Notices
utility or plant application filed under
35 U.S.C. 111(a) within the duration of
the pilot program; (3) the
nonprovisional application must
directly claim the benefit under 35
U.S.C. 119(e) and 37 CFR 1.78 of a prior
provisional application filed within the
previous 12 months, and the specific
reference to the provisional application
must be in an application data sheet
under 37 CFR 1.76 (see 37 CFR
1.78(a)(3)); and (4) the applicant must
not have filed a nonpublication request.
As required for all nonprovisional
applications, the applicant must satisfy
filing date requirements and publication
requirements. If the application
submitted on filing does not meet the
requirements for publication, or if the
application is filed without any claims,
the Office of Patent Application
Processing will issue an appropriate
notice setting a two-month (extendable)
time period within which to respond.
The Extended Missing Parts Pilot
Program does not change the two-month
time period set forth in any such notice.
In accordance with 35 U.S.C. 122(b), the
USPTO will publish the application
promptly after the expiration of 18
months from the earliest filing date for
which benefit is sought.
If the applicant satisfies the
requirements (discussed above) on filing
of the nonprovisional application and
the application is in condition for
publication, the USPTO will send the
applicant a Notice to File Missing Parts
of Nonprovisional Application that sets
a 12-month (non-extendable) time
period to submit the search fee, the
examination fee, any excess claims fees
(under 37 CFR 1.16(h)-(j)), and the
surcharge under 37 CFR 1.16(f) (for the
late submission of the search fee and
examination fee). If an applicant files a
timely reply to the Notice to File
Missing Parts within the 12-month time
period and the nonprovisional
application is completed, the
nonprovisional application will be
placed in the examination queue based
on the actual filing date of the
nonprovisional application.
For additional discussion, see Pilot
Program for Extended Time Period To
Reply to a Notice to File Missing Parts
of Nonprovisional Application, 75 FR
76401 (Dec. 8, 2010), 1362 Off. Gaz. Pat.
Office 44 (Jan. 4, 2011), and Extension
of the Extended Missing Parts Pilot
Program, 80 FR 80325 (Dec. 24, 2015),
1422 Off. Gaz. Pat. Office 192 (Jan. 19,
2016).
II. Request for Public Comments
The USPTO is requesting written
public comments on whether the
Extended Missing Parts Pilot Program
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17:04 Sep 02, 2016
Jkt 238001
should be made permanent. The USPTO
seeks input from the public on the
following:
1. Have you participated in the
Extended Missing Parts Pilot Program?
If so, please discuss what aspects of the
program you think are beneficial and
what aspects are not.
2. Please discuss why an applicant
would be discouraged from
participating in the Extended Missing
Parts Pilot Program.
3. Do you think the USPTO should
make the Extended Missing Parts Pilot
Program permanent? Why or why not?
4. Please provide any other input that
you would like the USPTO to consider
in determining whether the Extended
Missing Parts Pilot Program should be
made permanent.
Dated: August 29, 2016.
Russell Slifer,
Deputy Under Secretary of Commerce for
Intellectual Property and Deputy Director of
the United States Patent and Trademark
Office.
[FR Doc. 2016–21306 Filed 9–2–16; 8:45 am]
BILLING CODE 3510–16–P
DEPARTMENT OF COMMERCE
Patent and Trademark Office
[Docket No. PTO–C–2016–0032]
USPTO Cancer Moonshot Challenge
United States Patent and
Trademark Office, Commerce.
ACTION: Notice.
AGENCY:
The United States Patent and
Trademark Office (USPTO) publishes
this notice to announce the Cancer
Moonshot Challenge, which was
launched on August 22, 2016, to enlist
the public’s help to leverage the
USPTO’s intellectual property data,
often an early indicator of meaningful
research and development, and combine
it with other economic and funding
data. This challenge supports the goals
and objectives of the National Cancer
Moonshot, a Presidential initiative to
speed up cancer advances, make more
therapies available to more patients, and
improve the ability to prevent cancer
and detect it at an early stage. This
notice provides the public with
information on participation and
application requirements for the
challenge, including the judging criteria,
submission requirements, and rules of
eligibility.
SUMMARY:
Challenge Deadline: The
deadline for submissions is September
12, 2016, 5:00 p.m. Eastern Standard
Time (EST).
DATES:
PO 00000
Frm 00016
Fmt 4703
Sfmt 4703
All individuals or entities
who wish to participate in the challenge
must register and submit their entry
through www.challenge.gov.
FOR FURTHER INFORMATION CONTACT: For
further information, please contact
Thomas A. Beach, Office of the Under
Secretary and Director, at 571–272–
8600.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
I. About the Challenge
Background
Cancer is undoubtedly a disease that
touches all our lives. Ending cancer as
we know it requires the formation of
new alliances. As President Obama
noted, getting this done isn’t just going
to take the best and brightest across the
medical, research, and data
communities—but millions of
Americans owning a stake of it. By
harnessing the power of patent data and
accelerating the process for protecting
the intellectual property that leads to
cancer immunotherapy breakthroughs,
the USPTO is standing up and doing its
part to help bring potentially life-saving
treatments to patients, faster.
The Challenge
With data released through the
USPTO Developer Hub, users are
building rich visualizations of
intellectual property data, an early
indicator of meaningful innovation and
research and development (R&D), and
combining this data with other state or
agency data, such as census and bureau
of labor statistics, and/or economic and
financial data. These types of
visualizations demonstrate the power of
telling complex stories that lead to
impactful insights and ask why the data
matters. Similarly, we challenge you to
create and illuminate new trend lines
and interactive mappings of innovation
with visualizations for all types of
cancer treatments and diagnostics by
combining our data with other unique
data. Be sure to list the sources of your
data sets (i.e., orange book data from the
FDA), tools, and assumptions used to
form your conclusion and
visualizations. Imagine your data
visualizations will be the foundation to
empower the Federal Government—as
well as the medical, research, and data
communities—to make more precise
funding and policy decisions based on
the commercialization lifecycle of the
most promising treatments, while
maximizing U.S. competitiveness in
cancer investments.
Using analytic tools, processes, and
other interoperable data sets, we are
challenging you to develop interactive
visualizations and stories that can help
E:\FR\FM\06SEN1.SGM
06SEN1
Federal Register / Vol. 81, No. 172 / Tuesday, September 6, 2016 / Notices
reveal new insights to guide public
policy and research to achieve the goal
of doubling the rate of progress toward
a cure. For example, you could address
questions such as:
Trending:
• What new insights can be revealed
by correlating R&D spending/funding to
breakthrough technologies? How would
you define or cluster the broad spectrum
of cancer treatments, therapies, and/or
diagnostics?
• What would trace studies of
commercially successful treatments
from patent to product tell us? What
data insights can be gleaned from
understanding the time it takes bring
patents to patients?
• What are the peaks and valleys in
the landscape of cancer treatment
technologies?
Policy:
• If you were the Director of NIH or
another agency, given what you have
learned from this patent data and your
research, how would you prioritize your
cancer research budget? (The National
Cancer Institute’s FY2014 budget was
$4.932 billion.)
• Based on cluster mapping of cancer
treatments, therapies, and/or
diagnostics, what policy would you put
in place to promote certain
technologies? For example, would you
promote treatment to make cancer a
livable disease verses curing it?
• Is there any measurable relationship
between patent data, clinical trial data,
and time to it takes for the technology
to be in the hands of the patient? If so,
how (and with what catalyst for
innovation and policy changes) would
you advise the VPOTUS for the Cancer
Moonshot?
Moonshot can join today by visiting
www.whitehouse.gov/CancerMoonshot.
Resources
III. How To Enter
The USTPO has released a curated
data set consisting of 269,353 patent
documents (published patent
applications and granted patents)
spanning the 1976 to 2016 period. This
data and associated documentation
explaining our methodology can be
found on the USPTO Developer Hub.
By September 12, 2016, 5:00 p.m.
Eastern Standard Time, submit the
following items through
www.challenge.gov:
• A story (maximum 1,000 words).
Written in English, tell the story of your
visualization and walk users through
how to use your visualization. The
document must describe how your
visualization provides meaningful
insight, including potential actions and/
or discoveries.
• Access to and testing instructions
for your submission. This can be
appended to your visualization
description and does not count toward
the 1,000 word maximum.
• Link to the submission. We will not
accept any submission without a link.
Prizes
mstockstill on DSK3G9T082PROD with NOTICES
First Place: $5,000.00
Second Place: $3,000.00
Third Place: $2,000.00
More Information About the Cancer
Moonshot Initiative
As the President’s Cancer Moonshot
Initiative looks to build public-private
partnerships with industry,
governments, health systems, nonprofits, philanthropy, research
institutes, patients, and academia, those
interested in advancing the Cancer
VerDate Sep<11>2014
17:04 Sep 02, 2016
Jkt 238001
II. Judging Criteria
• Creativity & Innovation (20%)
Æ Uniqueness and innovation in
approach to revealing new insights
to guide public policy and research.
Æ Concept should be original, fill a
gap, or answer a question in a
manner that is not already
available.
• Evidence Base & Effectiveness (20%)
Æ Provide meaningful insight,
including potential actions and
discoveries, using patent-related
data to better inform funding and
policy decisions or uncover insights
into the cancer R&D process.
Æ How did you arrive at and validate
your story? Did you include
additional complimentary datasets
to help solidify your story? What
additional knowledge sources did
you use?
• Value to Public (20%)
Æ Concept should add value to the
medical, research, or data
communities and policymakers,
allowing them to make more
informed funding and policy
decisions based on the patterns and
trends of innovation in cancer
diagnosis and treatment.
• Usability (20%)
Æ The design elements should
attract, engage, and influence
actions from the public and
policymakers.
• Functional Product (20%)
Æ The visualization should have
demonstrable functionality as
described in project description.
IV. Rules
To be eligible to win a prize under
this challenge, an individual or entity:
PO 00000
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61197
(1) Shall have registered to participate
in the competition under the rules
promulgated by the USPTO.
(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; in the case of an individual,
whether participating singly or in a
group, shall be a citizen or permanent
resident of the United States.
(4) Shall not be a federal entity or
federal employee acting within the
scope of their employment.
(5) Shall not be a USPTO employee
working on their applications or
submissions during assigned duty
hours.
(6) In the case of a federal grantee,
shall not use federal funds to develop
applications unless consistent with the
purpose of their grant award.
(7) In the case of a federal contractor,
shall not use federal funds from a
contract to develop applications or to
fund efforts in support of a challenge
submission.
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
equitably available to all individuals
and entities participating in the
competition.
Entrants must 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 this prize contest,
whether the injury, death, damage, or
loss arises through negligence or
otherwise.
Entrants must also agree to indemnify
the Federal Government against thirdparty claims for damages arising from or
related to competition activities. By
entering into this competition, entrants
represent that the they possess liability
insurance or are otherwise financially
responsible for: (1) Claims by a third
party for death, bodily injury, or
property damage, or loss resulting from
an activity carried out in connection
with participation in the competition,
with the Federal Government named as
an additional insured under the
Entrant’s insurance policy, if any; and
(2) claims by the Federal Government
for damage or loss to government
property resulting from such an activity.
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61198
Federal Register / Vol. 81, No. 172 / Tuesday, September 6, 2016 / Notices
By submitting an entry to this
competition you represent and warrant
that your submission:
• Is your own work and not copied (if
we have reason to believe that your
submission is not your own work then
we may not consider it);
• does not contain any third party
intellectual property rights and/or
content that you do not have
permission to use; and
• is not obscene, defamatory, or in
breach of any applicable legislation or
regulations.
The USPTO reserves the right to
cancel, suspend, and/or modify the
challenge, or any part of it, for any
reason, at the USPTO’s sole discretion.
Submission Requirements
• Your submission must use at least
the cancer research dataset provided by
the USPTO.
• Your submission must be relevant
to a U.S. audience and must be in the
English language only.
• You are responsible for the cost and
expense (if any) of sending your
submission to us and, if your
submission is selected, either attending
an awards event demo at the USPTO on
September 26, 2016, in person or
submitting a video of your presentation
to be shared at the event.
• Only one project submission is
permitted per person or group. In the
event of a dispute over the identity of
an entrant, the submission will be
deemed submitted by the authorized
account holder of the email address
submitted during the registration
process.
Submissions that do not adhere to the
requirements listed above will be
automatically disqualified.
mstockstill on DSK3G9T082PROD with NOTICES
Intellectual Property
17:04 Sep 02, 2016
Dated: August 31, 2016.
Michelle K. Lee,
Under Secretary of Commerce for Intellectual
Property and Director of the United States
Patent and Trademark Office.
[FR Doc. 2016–21349 Filed 9–2–16; 8:45 am]
BILLING CODE 3510–16–P
CORPORATION FOR NATIONAL AND
COMMUNITY SERVICE
Information Collection; Submission for
OMB Review, Comment Request
Corporation for National and
Community Service.
ACTION: Notice.
AGENCY:
The Corporation for National
and Community Service (CNCS) has
submitted a public information
collection request (ICR) entitled Senior
Corps Project Progress Report (PPR)—
OMB Control Number 3045–0033 for
review and approval in accordance with
the Paperwork Reduction Act of 1995.
Copies of this ICR, with applicable
supporting documentation, may be
obtained by calling the Corporation for
National and Community Service, Jill
Sears, at 202–606–7577 or email to
jsears@cns.gov. Individuals who use a
telecommunications device for the deaf
(TTY–TDD) may call 1–800–833–3722
between 8:00 a.m. and 8:00 p.m. Eastern
Time, Monday through Friday.
DATES: Comments may be submitted,
identified by the title of the information
collection activity, within October 6,
2016.
SUMMARY:
Comments may be
submitted, identified by the title of the
information collection activity, to the
Office of Information and Regulatory
Affairs, Attn: Ms. Sharon Mar, OMB
Desk Officer for the Corporation for
National and Community Service, by
any of the following two methods
within 30 days from the date of
publication in the Federal Register:
(1) By fax to: 202–395–6974,
Attention: Ms. Sharon Mar, OMB Desk
Officer for the Corporation for National
and Community Service; or
(2) By email to: smar@omb.eop.gov.
SUPPLEMENTARY INFORMATION: The OMB
is particularly interested in comments
which:
• Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of CNCS, including whether
ADDRESSES:
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, publicly
perform, publicly display, and use the
submission to the extent necessary to
administer the challenge, and to
publicly perform and publicly display
the submission, including, without
limitation, for advertising and
promotional purposes relating to the
challenge.
VerDate Sep<11>2014
• All entrants are encouraged to open
source their code to the extent possible
as a continuing contribution to cancer
research.
Jkt 238001
PO 00000
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the information will have practical
utility;
• 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;
• Propose ways to enhance the
quality, utility, and clarity of the
information to be collected; and
• Propose ways to minimize the
burden of the collection of information
on those who are to respond, including
through the use of appropriate
automated, electronic, mechanical, or
other technological collection
techniques or other forms of information
technology.
Comments
A 60-day Notice requesting public
comment was published in the Federal
Register on 06/10/2016 at 81 FR 37582.
This comment period ended August 9,
2016. No public comments were
received from this Notice.
Description: The Senior Corps PPR
has two components: (1) Narratives and
work plans, and (2) the Progress Report
Supplement (PRS), which is an annual
survey of volunteer demographics and
grantee characteristics.
Type of Review: Renewal.
Agency: Corporation for National and
Community Service.
Title: Senior Corps Project Progress
Report.
OMB Number: 3045–0033.
Agency Number: None.
Affected Public: Sponsors of Senior
Corps grants.
Total Respondents: 1,250.
Frequency: Work plans and
narratives: Semi-Annual. Progress
Report Supplement: Annual.
Average Time per Response: Progress
Report and Supplement: Twelve hours.
Estimated Total Burden Hours: 15,000
hours.
Total Burden Cost (capital/startup):
None.
Total Burden Cost (operating/
maintenance): None.
Authority: Pub. L. 104–13, (44 U.S.C.
Chapter 35)
Dated: August 30, 2016.
Mikel Herrington,
Director, Senior Corps.
[FR Doc. 2016–21327 Filed 9–2–16; 8:45 am]
BILLING CODE 6050–28–P
E:\FR\FM\06SEN1.SGM
06SEN1
Agencies
[Federal Register Volume 81, Number 172 (Tuesday, September 6, 2016)]
[Notices]
[Pages 61196-61198]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-21349]
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
Patent and Trademark Office
[Docket No. PTO-C-2016-0032]
USPTO Cancer Moonshot Challenge
AGENCY: United States Patent and Trademark Office, Commerce.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The United States Patent and Trademark Office (USPTO)
publishes this notice to announce the Cancer Moonshot Challenge, which
was launched on August 22, 2016, to enlist the public's help to
leverage the USPTO's intellectual property data, often an early
indicator of meaningful research and development, and combine it with
other economic and funding data. This challenge supports the goals and
objectives of the National Cancer Moonshot, a Presidential initiative
to speed up cancer advances, make more therapies available to more
patients, and improve the ability to prevent cancer and detect it at an
early stage. This notice provides the public with information on
participation and application requirements for the challenge, including
the judging criteria, submission requirements, and rules of
eligibility.
DATES: Challenge Deadline: The deadline for submissions is September
12, 2016, 5:00 p.m. Eastern Standard Time (EST).
ADDRESSES: All individuals or entities who wish to participate in the
challenge must register and submit their entry through
www.challenge.gov.
FOR FURTHER INFORMATION CONTACT: For further information, please
contact Thomas A. Beach, Office of the Under Secretary and Director, at
571-272-8600.
SUPPLEMENTARY INFORMATION:
I. About the Challenge
Background
Cancer is undoubtedly a disease that touches all our lives. Ending
cancer as we know it requires the formation of new alliances. As
President Obama noted, getting this done isn't just going to take the
best and brightest across the medical, research, and data communities--
but millions of Americans owning a stake of it. By harnessing the power
of patent data and accelerating the process for protecting the
intellectual property that leads to cancer immunotherapy breakthroughs,
the USPTO is standing up and doing its part to help bring potentially
life-saving treatments to patients, faster.
The Challenge
With data released through the USPTO Developer Hub, users are
building rich visualizations of intellectual property data, an early
indicator of meaningful innovation and research and development (R&D),
and combining this data with other state or agency data, such as census
and bureau of labor statistics, and/or economic and financial data.
These types of visualizations demonstrate the power of telling complex
stories that lead to impactful insights and ask why the data matters.
Similarly, we challenge you to create and illuminate new trend lines
and interactive mappings of innovation with visualizations for all
types of cancer treatments and diagnostics by combining our data with
other unique data. Be sure to list the sources of your data sets (i.e.,
orange book data from the FDA), tools, and assumptions used to form
your conclusion and visualizations. Imagine your data visualizations
will be the foundation to empower the Federal Government--as well as
the medical, research, and data communities--to make more precise
funding and policy decisions based on the commercialization lifecycle
of the most promising treatments, while maximizing U.S. competitiveness
in cancer investments.
Using analytic tools, processes, and other interoperable data sets,
we are challenging you to develop interactive visualizations and
stories that can help
[[Page 61197]]
reveal new insights to guide public policy and research to achieve the
goal of doubling the rate of progress toward a cure. For example, you
could address questions such as:
Trending:
What new insights can be revealed by correlating R&D
spending/funding to breakthrough technologies? How would you define or
cluster the broad spectrum of cancer treatments, therapies, and/or
diagnostics?
What would trace studies of commercially successful
treatments from patent to product tell us? What data insights can be
gleaned from understanding the time it takes bring patents to patients?
What are the peaks and valleys in the landscape of cancer
treatment technologies?
Policy:
If you were the Director of NIH or another agency, given
what you have learned from this patent data and your research, how
would you prioritize your cancer research budget? (The National Cancer
Institute's FY2014 budget was $4.932 billion.)
Based on cluster mapping of cancer treatments, therapies,
and/or diagnostics, what policy would you put in place to promote
certain technologies? For example, would you promote treatment to make
cancer a livable disease verses curing it?
Is there any measurable relationship between patent data,
clinical trial data, and time to it takes for the technology to be in
the hands of the patient? If so, how (and with what catalyst for
innovation and policy changes) would you advise the VPOTUS for the
Cancer Moonshot?
Resources
The USTPO has released a curated data set consisting of 269,353
patent documents (published patent applications and granted patents)
spanning the 1976 to 2016 period. This data and associated
documentation explaining our methodology can be found on the USPTO
Developer Hub.
Prizes
First Place: $5,000.00
Second Place: $3,000.00
Third Place: $2,000.00
More Information About the Cancer Moonshot Initiative
As the President's Cancer Moonshot Initiative looks to build
public-private partnerships with industry, governments, health systems,
non-profits, philanthropy, research institutes, patients, and academia,
those interested in advancing the Cancer Moonshot can join today by
visiting www.whitehouse.gov/CancerMoonshot.
II. Judging Criteria
Creativity & Innovation (20%)
[cir] Uniqueness and innovation in approach to revealing new
insights to guide public policy and research.
[cir] Concept should be original, fill a gap, or answer a question
in a manner that is not already available.
Evidence Base & Effectiveness (20%)
[cir] Provide meaningful insight, including potential actions and
discoveries, using patent-related data to better inform funding and
policy decisions or uncover insights into the cancer R&D process.
[cir] How did you arrive at and validate your story? Did you
include additional complimentary datasets to help solidify your story?
What additional knowledge sources did you use?
Value to Public (20%)
[cir] Concept should add value to the medical, research, or data
communities and policymakers, allowing them to make more informed
funding and policy decisions based on the patterns and trends of
innovation in cancer diagnosis and treatment.
Usability (20%)
[cir] The design elements should attract, engage, and influence
actions from the public and policymakers.
Functional Product (20%)
[cir] The visualization should have demonstrable functionality as
described in project description.
III. How To Enter
By September 12, 2016, 5:00 p.m. Eastern Standard Time, submit the
following items through www.challenge.gov:
A story (maximum 1,000 words). Written in English, tell
the story of your visualization and walk users through how to use your
visualization. The document must describe how your visualization
provides meaningful insight, including potential actions and/or
discoveries.
Access to and testing instructions for your submission.
This can be appended to your visualization description and does not
count toward the 1,000 word maximum.
Link to the submission. We will not accept any submission
without a link.
IV. Rules
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 the USPTO.
(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; in the case
of an individual, whether participating singly or in a group, shall be
a citizen or permanent resident of the United States.
(4) Shall not be a federal entity or federal employee acting within
the scope of their employment.
(5) Shall not be a USPTO employee working on their applications or
submissions during assigned duty hours.
(6) In the case of a federal grantee, shall not use federal funds
to develop applications unless consistent with the purpose of their
grant award.
(7) In the case of a federal contractor, shall not use federal
funds from a contract to develop applications or to fund efforts in
support of a challenge submission.
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
equitably available to all individuals and entities participating in
the competition.
Entrants must 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 this prize contest,
whether the injury, death, damage, or loss arises through negligence or
otherwise.
Entrants must also agree to indemnify the Federal Government
against third-party claims for damages arising from or related to
competition activities. By entering into this competition, entrants
represent that the they possess liability insurance or are otherwise
financially responsible for: (1) Claims by a third party for death,
bodily injury, or property damage, or loss resulting from an activity
carried out in connection with participation in the competition, with
the Federal Government named as an additional insured under the
Entrant's insurance policy, if any; and (2) claims by the Federal
Government for damage or loss to government property resulting from
such an activity.
[[Page 61198]]
By submitting an entry to this competition you represent and
warrant that your submission:
Is your own work and not copied (if we have reason to believe
that your submission is not your own work then we may not consider it);
does not contain any third party intellectual property rights
and/or content that you do not have permission to use; and
is not obscene, defamatory, or in breach of any applicable
legislation or regulations.
The USPTO reserves the right to cancel, suspend, and/or modify the
challenge, or any part of it, for any reason, at the USPTO's sole
discretion.
Submission Requirements
Your submission must use at least the cancer research
dataset provided by the USPTO.
Your submission must be relevant to a U.S. audience and
must be in the English language only.
You are responsible for the cost and expense (if any) of
sending your submission to us and, if your submission is selected,
either attending an awards event demo at the USPTO on September 26,
2016, in person or submitting a video of your presentation to be shared
at the event.
Only one project submission is permitted per person or
group. In the event of a dispute over the identity of an entrant, the
submission will be deemed submitted by the authorized account holder of
the email address submitted during the registration process.
Submissions that do not adhere to the requirements listed above
will be automatically disqualified.
Intellectual Property
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,
publicly perform, publicly display, and use the submission to the
extent necessary to administer the challenge, and to publicly perform
and publicly display the submission, including, without limitation, for
advertising and promotional purposes relating to the challenge.
All entrants are encouraged to open source their code to
the extent possible as a continuing contribution to cancer research.
Dated: August 31, 2016.
Michelle K. Lee,
Under Secretary of Commerce for Intellectual Property and Director of
the United States Patent and Trademark Office.
[FR Doc. 2016-21349 Filed 9-2-16; 8:45 am]
BILLING CODE 3510-16-P