Pandemic Influenza Vaccines-Amendment, 10268-10272 [2010-4644]
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10268
Federal Register / Vol. 75, No. 43 / Friday, March 5, 2010 / Notices
1448 or e-mail at
beverly.cromer@gsa.gov.
DEPARTMENT OF DEFENSE
GENERAL SERVICES
ADMINISTRATION
SUPPLEMENTARY INFORMATION:
A. Purpose
If it is in the best interest of the
Government, the contracting officer may
authorize cost-reimbursement
contractors to obtain, for official
purposes only, interagency motor pool
vehicles and related services.
Contractors’ requests for vehicles must
obtain two copies of the agency
authorization, the number of vehicles
and related services required and period
of use, a list of employees who are
authorized to request the vehicles, a
listing of equipment authorized to be
serviced, and billing instructions and
address. A written statement that the
contractor will assume, without the
right of reimbursement from the
Government, the cost or expense of any
use of the motor pool vehicles and
services not related to the performance
of the contract is necessary before the
contracting officer may authorize costreimbursement contractors to obtain
interagency motor pool vehicles and
related services.
The information is used by the
Government to determine that it is in
the Government’s best interest to
authorize a cost-reimbursement
contractor to obtain, for official
purposes only, interagency motor pool
vehicles and related services, and to
provide those vehicles.
B. Annual Reporting Burden
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Respondents: 70.
Responses per Respondent: 2.
Annual Responses: 140.
Hours per Response: .5.
Total Burden Hours: 70.
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. 9000–0032,
Contractor Use of Interagency Motor
Pool Vehicles, in all correspondence.
Dated: February 26, 2010.
Al Matera,
Director, Acquisition Policy Division.
[FR Doc. 2010–4655 Filed 3–4–10; 8:45 am]
BILLING CODE 6820–EP–P
NATIONAL AERONAUTICS AND
SPACE ADMINISTRATION
[OMB Control No. 9000–0034; Docket 2010–
0083; Sequence 13]
Federal Acquisition Regulation;
Information Collection; Examination of
Records by Comptroller General and
Contract Audit
AGENCIES: Department of Defense (DOD),
General Services Administration (GSA),
and National Aeronautics and Space
Administration (NASA).
ACTION: Notice of request for public
comments regarding an extension to an
existing OMB clearance.
SUMMARY: Under the provisions of the
Paperwork Reduction Act of 1995 (44
U.S.C. Chapter 35), the Regulatory
Secretariat will be submitting to the
Office of Management and Budget
(OMB) a request to review and approve
an extension of a previously approved
information collection requirement
concerning the examination of records
by comptroller general and contract
audit.
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
May 4, 2010.
ADDRESSES: Submit comments regarding
this burden estimate or any other aspect
of the collection of information,
including suggestions for reducing this
burden to the General Services
Administration, Regulatory Secretariat
(MVCB), 1800 F Street, NW., Room
4041, Washington, DC 20405.
FOR FURTHER INFORMATION CONTACT: Mr.
Michael Jackson, Procurement Analyst,
Contract Policy Branch, GSA, (202) 208–
4949 or e-mail
michaelo.jackson@gsa.gov.
SUPPLEMENTARY INFORMATION:
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A. Purpose
The Audit and Records-Negotiation
clause, 52.215–2; Contract Terms and
Conditions Required to Implement
Statutes or Executive Orders—
Commercial Items clause, 52.212–5(d);
and Audit and Records-Sealed Bidding
clause, 52.214–26, implement the
requirements of 10 U.S.C. 2313, 41
U.S.C. 254, and 10 U.S.C. 2306. The
statutory requirements are that the
Comptroller General and/or agency shall
have access to, and the right to, examine
certain books, documents and records of
the contractor for a period of 3 years
after final payment. The record
retention periods required of the
contractor in the clauses are for
compliance with the aforementioned
statutory requirements. The information
must be retained so that audits
necessary for contract surveillance,
verification of contract pricing, and
reimbursement of contractor costs can
be performed.
B. Annual Reporting Burden
Respondents: 19,142.
Responses per Respondent: 20.
Total Responses: 382,840.
Hours per Response: 0.167.
Total Burden Hours: 63,934.
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 Number 9000–
0034, Examination of Records by
Comptroller General and Contract
Audit, in all correspondence.
Dated: February 26, 2010.
Al Matera,
Director, Acquisition Policy Division.
[FR Doc. 2010–4590 Filed 3–4–10; 8:45 am]
BILLING CODE 6820–EP–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Pandemic Influenza Vaccines—
Amendment
Authority: 42 U.S.C. 247d–6d.
Notice of amendment to the
September 28, 2009 Republished
Declaration under the Public Readiness
and Emergency Preparedness Act.
ACTION:
SUMMARY: Amendment to declaration
issued on September 28, 2009 (74 FR
51153) pursuant to section 319F–3 of
the Public Health Service Act (‘‘the Act’’)
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(42 U.S.C. 247d–6d) to revise covered
countermeasures and extend effective
date and republication of the
declaration to reflect the declaration in
its entirety, as amended.
DATES: The amendment of the
republished declaration issued on
September 28, 2009 is effective as of
March 1, 2010.
FOR FURTHER INFORMATION CONTACT:
Nicole Lurie, MD, MSPH, Assistant
Secretary for Preparedness and
Response, Office of the Secretary,
Department of Health and Human
Services, 200 Independence Avenue,
SW., Washington, DC 20201, Telephone
(202) 205–2882 (this is not a toll-free
number).
HHS Secretary’s Amendment to the
September 28, 2009 Republished
Declaration for the Use of the Public
Readiness and Emergency Preparedness
Act for H5N1, H2, H6, H7, H9 and
2009–H1N1 Vaccines:
Whereas there are or may be multiple
animal influenza A viruses, circulating
in wild birds and/or domestic animals
that cause, or have significant potential
to cause, sporadic human infections or
have mutated to cause pandemics in
humans;
Whereas, these viruses may evolve
into virus strains capable of causing a
pandemic of human influenza because
these viruses may cause infection in and
spread among humans and because
humans have little or no immunity to
these viruses;
Whereas, one such virus is the 2009
H1N1 Influenza Virus;
Whereas, vaccination may be effective
to protect persons from the threat of
pandemic influenza;
Whereas, Secretary Michael O. Leavitt
issued a Declaration for the Use of the
Public Readiness and Emergency
Preparedness Act dated January 26,
2007 (‘‘Original Declaration’’), as
amended on November 30, 2007 and
October 17, 2008 with respect to certain
avian influenza viruses;
Whereas, I amended the declaration
on June 15, 2009 with respect to 2009
H1N1 influenza virus and on September
28, 2009 to provide targeted liability
protections for pandemic
countermeasures to enhance
distribution and to add provisions
consistent with other declarations, and
republished the declaration each time in
its entirety;
Whereas, the September 28, 2009
declaration extended through February
28, 2010 for vaccines against influenza
virus strains named in the Declaration
other than 2009 H1N1 influenza
vaccine;
Whereas, modifications are necessary
to revise covered countermeasures and
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to extend the effective date of the
Declaration;
Whereas, the findings I made in the
declaration issued on September 28,
2009 continue to apply;
Whereas, in accordance with section
319F–3(b)(6) of the Act (42 U.S.C. 247d–
6d(b)), I have considered the desirability
of encouraging the design, development,
clinical testing or investigation,
manufacturing, labeling, distribution,
formulation, packaging, marketing,
promotion, sale, purchase, donation,
dispensing, prescribing, administration,
licensing, and use of additional covered
countermeasures with respect to the
category of disease and population
described in sections II and IV of the
September 28, 2009 Republished
Declaration, as hereby amended, and
have found it desirable to encourage
such activities for these additional
covered countermeasures, and;
Whereas, to encourage the design,
development, clinical testing or
investigation, manufacturing and
product formulation, labeling,
distribution, packaging, marketing,
promotion, sale, purchase, donation,
dispensing, prescribing, administration,
licensing, and use of medical
countermeasures with respect to the
category of disease and population
described in sections II and IV of the
September 28, 2009 Republished
Declaration, as hereby amended, it is
advisable, in accordance with section
319F–3(a) and (b) of the Act, to provide
immunity from liability for covered
persons, as that term is defined at
section 319F–3(i)(2) of the Act, and to
include as such covered persons other
qualified persons as I have identified in
section VI of the September 28, 2009
Republished Declaration, as amended;
Therefore, pursuant to section 319F–
3(b) of the Act, I have determined that
there is a credible risk that the spread
of influenza A viruses with pandemic
potential and resulting disease could in
the future constitute a public health
emergency and that spread of one of
these viruses (2009 H1N1 Influenza) has
caused a disease that constitutes a
public health emergency.
In order to extend the scope of
covered countermeasures and to extend
the effective date of the Declaration, the
September 28, 2009 Republished
Declaration, is hereby amended as
follows:
In the title, delete ‘‘for H5N1, H2, H6,
H7, H9 and 2009 H1N1 Vaccines’’ and
replace with ‘‘for Vaccines Against
Pandemic Influenza A Viruses and
Those with Pandemic Potential’’.
In the recitals, delete the first through
the fourth ‘‘whereas’’ clauses, and insert
two new recitals as follows:
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Whereas there are or may be multiple
animal influenza A viruses circulating
in wild birds and/or domestic animals
that cause, or have significant potential
to cause, sporadic human infections or
have mutated to cause pandemics in
humans;
Whereas, these viruses may evolve or
have evolved into virus strains capable
of causing a pandemic of human
influenza because these viruses may
cause infection in, and spread among,
humans and because humans have little
or no immunity to these viruses;
In the sixth ‘‘whereas’’ clause, insert
‘‘October 1, 2009, and December 28,
2009’’ after ‘‘July 24, 2009’’.
In the ‘‘therefore’’ clause, delete ‘‘avian
influenza viruses and resulting disease
could in the future constitute a public
health emergency, and that 2009 H1N1
influenza constitutes a public health
emergency’’ and replace with:
‘‘pandemic influenza A viruses and
those with pandemic potential and
resulting disease does or could
constitute a public health emergency’’.
In section I, first paragraph, delete
‘‘the pandemic countermeasures
influenza A H5N1, H2, H6, H7, H9, and
2009 H1N1 vaccines’’ each time it
appears and replace with ‘‘vaccines
against pandemic influenza A viruses
with pandemic potential’’.
In section I, at the end of the second
sentence, replace ‘‘IX’’ with ‘‘X’’.
In section II, delete ‘‘the virus with (1)
highly pathogenic avian influenza A
(H5N1, H2, H6, H7, or H9) virus; or (2)
2009 H1N1 influenza’’ and replace with
‘‘animal and/or human influenza A
viruses against which most humans do
not have immunity, except those
included in seasonal influenza vaccines
and/or covered under the National
Vaccine Injury Compensation Program,
that are circulating in wild birds and/or
domestic animals causing or having
significant potential to cause sporadic
human infections or have mutated to
cause pandemics in humans’’.
In section III, first paragraph, delete in
its entirety and replace with: ‘‘The
effective period of time of this
Declaration commenced as described in
the September 28, 2009 Republished
Declaration, and extends through
February 28, 2012.
In section III, second paragraph,
delete ‘‘; except that with respect to 2009
H1N1 influenza vaccine, the effective
period commences on June 15, 2009 and
extends through March 31, 2013’’ and
replace with ‘‘through February 28,
2012.’’
In section III, add to the end of the
section as a new paragraph: ‘‘With
respect to any covered countermeasure
subsequently covered under the
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National Vaccine Injury Compensation
Program, the effective time period
expires immediately upon such
coverage.’’
In section VIII, insert ‘‘and use’’ after
‘‘administration in the first sentence,
delete ‘‘the Act’s’’ from the second
sentence and replace with ‘‘this’’, and
delete ‘‘Countermeasure’’ from the
second sentence and replace with
‘‘Countermeasures’’.
In section IX, add to the end of the
first sentence: ‘‘; and amended on
September 28, 2009 to provide targeted
liability protections for pandemic
countermeasures to enhance
distribution and to add provisions
consistent with other declarations and
republished in its entirety.’’
In section X, after the fifth paragraph,
insert a new definition as follows:
Pandemic influenza A viruses and
those with pandemic potential: Animal
and/or human influenza A viruses,
except those included in seasonal
influenza vaccines and/or covered
under the National Vaccine Injury
Compensation Program, that are
circulating in wild birds and/or
domestic animals, that cause, or have
significant potential to cause, sporadic
or ongoing human infections, or
historically have caused pandemics in
humans, or have mutated to cause
pandemics in humans, and for which
the majority of the population is
¨
immunologically naıve.
In Appendix I, title and item 32, add
‘‘H7,’’ after ‘‘H6’’.
Throughout, insert ‘‘National’’ before
‘‘Vaccine Injury Compensation Fund’’.
All other provisions of the June 15,
2009 Republished Declaration remain in
full force.
Republication of HHS Secretary’s
September 28, 2009 Republished
Declaration, as Amended, for the Use of
the Public Readiness and Emergency
Preparedness Act for Vaccines Against
Pandemic Influenza A Viruses and
Those with Pandemic Potential.
To the extent any term of the
September 28 Republished Declaration,
as hereby amended, is inconsistent with
any provision of this Republished
Declaration, the terms of this
Republished Declaration are controlling.
Whereas there are or may be multiple
animal influenza A viruses circulating
in wild birds and/or domestic animals
that cause, or have significant potential
to cause, sporadic human infections or
have mutated to cause pandemics in
humans;
Whereas, these viruses may evolve or
have evolved into virus strains capable
of causing a pandemic of human
influenza because these viruses may
cause infection in, and spread among,
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humans and because humans have little
immunity to these viruses;
Whereas, on April 26, 2009, Acting
Secretary Charles E. Johnson
determined under section 319 of the
Public Health Service Act, (42 U.S.C.
247d), that a public health emergency
exists nationwide involving the Swine
Influenza A virus that affects or has
significant potential to affect the
national security (now called ‘‘2009–
H1N1 influenza’’);
Whereas, on July 24, 2009, October 1,
2009, and December 28, 2009 I renewed
the determination by the Acting
Secretary that a public health
emergency exists nationwide involving
the Swine influenza A virus (now called
‘‘2009–H1N1 influenza virus’’);
Whereas, vaccination may be effective
to protect persons from the threat of
pandemic influenza;
Whereas, the possibility of
governmental program planners
obtaining stockpiles from private sector
entities except through voluntary means
such as commercial sale, donation, or
deployment would undermine national
preparedness efforts and should be
discouraged as provided for in section
319F–3(b)(2)(E) of the Public Health
Service Act (42 U.S.C. 247d–6d(b)) (‘‘the
Act’’);
Whereas, immunity under section
319F–3(a) of the Act should be available
to governmental program planners for
distributions of Covered
Countermeasures obtained voluntarily,
such as by (1) donation; (2) commercial
sale; (3) deployment of Covered
Countermeasures from Federal
stockpiles; or (4) deployment of
donated, purchased, or otherwise
voluntarily obtained Covered
Countermeasures from State, local, or
private stockpiles;
Whereas, the extent of immunity
under section 319F–3(a) of the Act
afforded to a governmental program
planner that obtains Covered
Countermeasures except through
voluntary means is not intended to
affect the extent of immunity afforded
other covered persons with respect to
such covered countermeasures;
Whereas, to encourage the design,
development, clinical testing or
investigation, manufacturing and
product formulation, labeling,
distribution, packaging, marketing,
promotion, sale, purchase, donation,
dispensing, prescribing, administration,
licensing, and use of medical
countermeasures with respect to the
category of disease and population
described in section II and IV it is
advisable, in accordance with section
319F–3(a) and (b) of the Act, to provide
immunity from liability for covered
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persons, as that term is defined at
section 319F–3(i)(2) of the Act, and to
include as such covered persons such
other qualified persons as I have
identified in section VI;
Whereas, in accordance with section
319F–3(b)(6) of the Public Health
Service Act (42 U.S.C. 247d–6d(b)) (‘‘the
Act’’), I have considered the desirability
of encouraging the design, development,
clinical testing or investigation,
manufacturing and product formulation,
labeling, distribution, packaging,
marketing, promotion, sale, purchase,
donation, dispensing, prescribing,
administration, licensing, and use of
medical countermeasures with respect
to the category of disease and
population described in sections II and
IV below, and have found it desirable to
encourage such activities for the
Covered Countermeasures;
Therefore, pursuant to section 319F–
3(b) of the Act, I have determined there
is a credible risk that the spread of
pandemic influenza A viruses and those
with pandemic potential and resulting
disease does or could constitute a public
health emergency.
I. Covered Countermeasures (as
Required by Section 319F–3(b)(1) of the
Act)
Covered Countermeasures are defined
at section 319F–3(i) of the Act.
At this time, and in accordance with
the provisions contained herein, I am
recommending the manufacture, testing,
development, distribution, dispensing;
and, with respect to the category of
disease and population described in
sections II and IV, below, the
administration and usage of vaccines
against influenza A viruses with
pandemic potential and any associated
adjuvants. The immunity specified in
section 319F–3(a) of the Act shall only
be in effect with respect to: (1) Present
or future Federal contracts, cooperative
agreements, grants, interagency
agreements, or memoranda of
understanding for vaccines against
pandemic influenza A viruses with
pandemic potential used and
administered in accordance with this
declaration, and (2) activities authorized
in accordance with the public health
and medical response of the Authority
Having Jurisdiction to prescribe,
administer, deliver, distribute or
dispense the pandemic countermeasures
following a declaration of an emergency,
as defined in section X below. In
accordance with section 319F–3(b)(2)(E)
of the Act, for governmental program
planners, the immunity specified in
section 319F–3(a) of the Act shall be in
effect to the extent they obtain Covered
Countermeasures through voluntary
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means of distribution, such as (1)
donation; (2) commercial sale; (3)
deployment of Covered
Countermeasures from Federal
stockpiles; or (4) deployment of
donated, purchased, or otherwise
voluntarily obtained Covered
Countermeasures from State, local, or
private stockpiles. For all other covered
persons, including other program
planners, the immunity specified in
section 319F–3(a) of the Act shall, in
accordance with section 319F–3(b)(2)(E)
of the Act, be in effect pursuant to any
means of distribution.
This Declaration shall subsequently
refer to the countermeasures identified
above as Covered Countermeasures.
This Declaration shall apply to all
Covered Countermeasures administered
or used during the effective time period
of the Declaration.
II. Category of Disease (as Required by
Section 319F–3(b)(2)(A) of the Act)
The category of disease for which I am
recommending the administration or
use of the Covered Countermeasures is
the threat of or actual human influenza
that results from the infection of
humans following exposure to animal
and/or human influenza A viruses,
against which most humans do not have
immunity, except those included in
seasonal influenza vaccines and/or
covered under the National Vaccine
Injury Compensation Program, that are
circulating in wild birds and/or
domestic animals causing or have
significant potential to cause sporadic
human infections or have mutated to
cause pandemics in humans.
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III. Effective Time Period (as Required
by Section 319F–3(b)(2)(B) of the Act)
The effective period of time of this
Declaration commenced as described in
the September 28, 2009 Republished
Declaration and extends through
February 28, 2012.
With respect to Covered
Countermeasures administered and
used in accordance with the public
health and medical response of the
Authority Having Jurisdiction, the
effective period of time of this
Declaration commences on the date of a
declaration of an emergency and lasts
through and includes the final day that
the emergency declaration is in effect
including any extensions thereof
through February 28, 2012.
With respect to any covered
countermeasure subsequently covered
under the National Vaccine Injury
Compensation Program, the effective
time period expires immediately upon
such coverage.
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IV. Population (as Required by Section
319F–3(b)(2)(C) of the Act)
Section 319F–3(a)(4)(A) confers
immunity to manufacturers and
distributors of the Covered
Countermeasure, regardless of the
defined population.
Section 319F–3(a)(3)(C)(i) confers
immunity to covered persons who could
be program planners or qualified
persons with respect to the Covered
Countermeasure only if a member of the
population specified in the Declaration
administers or uses the Covered
Countermeasure and is in or connected
to the geographic location specified in
this Declaration, or the program planner
or qualified person reasonably could
have believed that these conditions
were met.
The populations specified in this
Declaration are the following:
(1) All persons who use a Covered
Countermeasure or to whom such a
Covered Countermeasure is
administered as an Investigational New
Drug in a human clinical trial
conducted directly by the Federal
Government, or pursuant to a contract,
grant or cooperative agreement with the
Federal Government; (2) all persons
who use a Covered Countermeasure or
to whom such a Countermeasure is
administered in a pre-pandemic phase,
as defined below; and/or (3) all persons
who use a Covered Countermeasure, or
to whom such a Covered
Countermeasure is administered in a
pandemic phase, as defined below.
V. Geographic Area (as Required by
Section 319F–3(b)(2)(D) of the Act)
Section 319F–3(a) applies to the
administration and use of a Covered
Countermeasure without geographic
limitation.
VI. Other Qualified Persons (as
Required by Section 319F–3(i)(8)(B) of
the Act)
With regard to the administration or
use of a Covered Countermeasure,
Section 319F–3(i)(8)(A) of the Act
defines the term ‘‘qualified person’’ as a
licensed individual who is authorized to
prescribe, administer, or dispense the
countermeasure under the law of the
State in which such Covered
Countermeasure was prescribed,
administered or dispensed. Additional
persons who are qualified persons
pursuant to section 319F–3(i)(8)(B) are
the following: (1) Any person
authorized in accordance with the
public health and medical emergency
response of the Authority Having
Jurisdiction to prescribe, administer,
deliver, distribute or dispense Covered
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10271
Countermeasures, and their officials,
agents, employees, contractors and
volunteers, following a declaration of an
emergency, and (2) Any person
authorized to prescribe, administer, or
dispense Covered Countermeasures or
who is otherwise authorized under an
Emergency Use Authorization.
VII. Additional Time Periods of
Coverage After Expiration of
Declaration (as Required by Section
319F–3(b)(3)(B) of the Act)
A. I have determined that, upon
expiration of the applicable time period
specified in Section III above, an
additional twelve (12) months is a
reasonable period to allow for the
manufacturer to arrange for disposition
of the Covered Countermeasure,
including the return of such product to
the manufacturer, and for covered
persons to take such other actions as are
appropriate to limit the administration
or use of the Covered Countermeasure,
and the liability protection of section
319F–3(a) of the Act shall extend for
that period.
B. The Federal Government shall
purchase the entire production of
Covered Countermeasures under the
contracts specifically listed by contract
number in section I for the stockpile
under section 319F–2 of the Act, and
shall be subject to the time-period
extension of section 319F–3(b)(3)(C).
Production under future contracts for
the same vaccine will also be subject to
the time-period extension of section
319F–3(b)(3)(C).
VIII. Compensation Fund
In addition to conferring immunity to
manufacturers, distributors, and
administrators of the Covered
Countermeasures, the Act provides
benefits to certain individuals who
sustain a covered injury as the direct
result of the administration or use of the
Covered Countermeasure. The
Countermeasures Injury Compensation
Program (CICP) within the Health
Resources and Services Administration
(HRSA) administers this compensation
program. Information about the CICP is
available at 1–888–275–4772 or https://
www.hrsa.gov/countermeasurescomp/
default.htm.
IX. Amendments
The Declaration for the Use of the
Public Readiness and Emergency
Preparedness Act for H5N1 was
published on January 26, 2007;
amended on November 30, 2007 to add
H7 and H9 vaccines; amended on
October 17, 2008 to add H2 and H6
vaccines; amended on June 15, 2009 to
add 2009 H1N1 vaccines and
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republished in its entirety; and
amended on September 28, 2009 to
provide targeted liability protections for
pandemic countermeasures to enhance
distribution and to add provisions
consistent with other declarations and
republished in its entirety. This
Declaration incorporates all
amendments prior to the date of its
publication in the Federal Register. Any
future amendment to this Declaration
will be published in the Federal
Register, pursuant to section 319F–
2(b)(4) of the Act.
X. Definitions
For the purpose of this Declaration,
including any claim for loss brought in
accordance with section 319F–3 of the
PHS Act against any covered persons
defined in the Act or this Declaration,
the following definitions will be used:
Administration of a Covered
Countermeasure: As used in section
319F–3(a)(2)(B) of the Act includes, but
is not limited to, public and private
delivery, distribution, and dispensing
activities relating to physical
administration of the countermeasures
to recipients, management and
operation of delivery systems, and
management and operation of
distribution and dispensing locations.
Authority Having Jurisdiction: Means
the public agency or its delegate that has
legal responsibility and authority for
responding to an incident, based on
political or geographical (e.g., city,
county, Tribal, State, or Federal
boundary lines) or functional (e.g., law
enforcement, public health) range or
sphere of authority.
Covered Persons: As defined at
section 319F–3(i)(2) of the Act, include
the United States, manufacturers,
distributors, program planners, and
qualified persons. The terms
‘‘manufacturer,’’ ‘‘distributor,’’ ‘‘program
planner,’’ and ‘‘qualified person’’ are
further defined at sections 319F–3(i)(3),
(4), (6), and (8) of the Act.
Declaration of Emergency: A
declaration by any authorized local,
regional, State, or Federal official of an
emergency specific to events that
indicate an immediate need to
administer and use pandemic
countermeasures, with the exception of
a Federal declaration in support of an
emergency use authorization under
section 564 of the FDCA unless such
declaration specifies otherwise.
Pandemic influenza A viruses and
those with pandemic potential: Animal
and/or human influenza A viruses,
except those included in seasonal
influenza vaccines and/or covered
under the National Vaccine Injury
Compensation Program, that are
VerDate Nov<24>2008
14:45 Mar 04, 2010
Jkt 220001
circulating in wild birds and/or
domestic animals, that cause, or have
significant potential to cause, sporadic
or ongoing human infections, or
historically have caused pandemics in
humans, or have mutated to cause
pandemics in humans, and for which
the majority of the population is
¨
immunologically naıve.
Pandemic Phase: The following
stages, as defined in the National
Strategy for Pandemic Influenza:
Implementation Plan (Homeland
Security Council, May 2006): (4) First
Human Case in North America; and (5)
Spread Throughout United States.
Pre-pandemic Phase: The following
stages, as defined in the National
Strategy for Pandemic Influenza:
Implementation Plan (Homeland
Security Council, May 2006): (0) New
Domestic Animal Outbreak in At-Risk
Country; (1) Suspected Human Outbreak
Overseas; (2) Confirmed Human
Outbreak Overseas; and (3) Widespread
Human Outbreaks in Multiple Locations
Overseas.
Dated: February 26, 2010.
Kathleen Sebelius,
Secretary.
APPENDIX
I. List of U.S. Government Contracts—
Covered H5N1, H2, H6, H7, H9, and 2009–
H1N1 Vaccine Contracts
1. HHSN266200400031C
2. HHSN266200400032C
3. HHSN266200300039C
4. HHSN266200400045C
5. HHSN266200205459C
6. HHSN266200205460C
7. HHSN266200205461C
8. HHSN266200205462C
9. HHSN266200205463C
10. HHSN266200205464C
11. HHSN266200205465C
12. HHSN266199905357C
13. HHSN266200300068C
14. HHSN266200005413C
15. HHSO100200600021C (formerly
200200409981)
16. HHSO100200500004C
17. HHSO100200500005I
18. HHSO100200700026I
19. HHSO100200700027I
20. HHSO100200700028I
21. HHSO100200600010C
22. HHSO100200600011C
23. HHSO100200600012C
24. HHSO100200600013C
25. HHSO100200600014C
26. HHSO100200600022C (formerly
200200511758)
27. HHSO100200600023C (formerly
200200410431)
28. CRADA No. AI–0155 NIAID/MedImmune
29. HHSO100200700029C
30. HHSO100200700030C
31. HHSO100200700031C
32. All present, completed and future
Government H5N1, H2, H6, H7, H9, and
2009–H1N1 vaccine contracts not
PO 00000
Frm 00069
Fmt 4703
Sfmt 4703
otherwise listed.
[FR Doc. 2010–4644 Filed 3–4–10; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Notice Regarding 340B Drug Pricing
Program—Contract Pharmacy Services
AGENCY: Health Resources and Services
Administration, HHS.
ACTION: Final notice.
SUMMARY: Section 602 of Public Law
102–585, the ‘‘Veterans Health Care Act
of 1992’’ enacted Section 340B of the
Public Health Service Act (PHS).
Section 340B implements a drug pricing
program by which manufacturers who
sell covered outpatient drugs to
particular covered entities listed in the
statute must agree to charge a price that
will not exceed the amount determined
under a statutory formula. The purpose
of this Final Notice is to inform
interested parties of final guidelines
regarding the utilization of multiple
contract pharmacies and suggested
contract pharmacy provisions, which
had been previously limited to the
Alternative Methods Demonstration
Project program.
FOR FURTHER INFORMATION CONTACT: Mr.
Jimmy Mitchell, Director, Office of
Pharmacy Affairs (OPA), Healthcare
Systems Bureau (HSB), Health
Resources and Services Administration
(HRSA), 5600 Fishers Lane, Parklawn
Building, Room 10C–03, Rockville,
Maryland 20857 or by telephone
through the Pharmacy Services Support
Center at 1–800–628–6297.
DATES: Effective Date: April 5, 2010.
SUPPLEMENTARY INFORMATION:
A. Background
Proposed guidelines for contract
pharmacy services were announced in
the Federal Register at 72 FR 1540 on
January 12, 2007. A comment period of
60 days was established to allow
interested parties to submit comments.
HRSA, HSB, acting through the OPA,
received 32 comments concerning the
proposal.
In 1996, HRSA issued guidelines that
permitted covered entities participating
in the 340B Drug Pricing Program to
contract with a pharmacy to provide
services to the covered entity’s patients
(61 FR 43549, August 23, 1996). Those
guidelines permitted a covered entity to
use a single point for pharmacy services,
either an in-house pharmacy or an
E:\FR\FM\05MRN1.SGM
05MRN1
Agencies
[Federal Register Volume 75, Number 43 (Friday, March 5, 2010)]
[Notices]
[Pages 10268-10272]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-4644]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
Pandemic Influenza Vaccines--Amendment
Authority: 42 U.S.C. 247d-6d.
ACTION: Notice of amendment to the September 28, 2009 Republished
Declaration under the Public Readiness and Emergency Preparedness Act.
-----------------------------------------------------------------------
SUMMARY: Amendment to declaration issued on September 28, 2009 (74 FR
51153) pursuant to section 319F-3 of the Public Health Service Act
(``the Act'')
[[Page 10269]]
(42 U.S.C. 247d-6d) to revise covered countermeasures and extend
effective date and republication of the declaration to reflect the
declaration in its entirety, as amended.
DATES: The amendment of the republished declaration issued on September
28, 2009 is effective as of March 1, 2010.
FOR FURTHER INFORMATION CONTACT: Nicole Lurie, MD, MSPH, Assistant
Secretary for Preparedness and Response, Office of the Secretary,
Department of Health and Human Services, 200 Independence Avenue, SW.,
Washington, DC 20201, Telephone (202) 205-2882 (this is not a toll-free
number).
HHS Secretary's Amendment to the September 28, 2009 Republished
Declaration for the Use of the Public Readiness and Emergency
Preparedness Act for H5N1, H2, H6, H7, H9 and 2009-H1N1 Vaccines:
Whereas there are or may be multiple animal influenza A viruses,
circulating in wild birds and/or domestic animals that cause, or have
significant potential to cause, sporadic human infections or have
mutated to cause pandemics in humans;
Whereas, these viruses may evolve into virus strains capable of
causing a pandemic of human influenza because these viruses may cause
infection in and spread among humans and because humans have little or
no immunity to these viruses;
Whereas, one such virus is the 2009 H1N1 Influenza Virus;
Whereas, vaccination may be effective to protect persons from the
threat of pandemic influenza;
Whereas, Secretary Michael O. Leavitt issued a Declaration for the
Use of the Public Readiness and Emergency Preparedness Act dated
January 26, 2007 (``Original Declaration''), as amended on November 30,
2007 and October 17, 2008 with respect to certain avian influenza
viruses;
Whereas, I amended the declaration on June 15, 2009 with respect to
2009 H1N1 influenza virus and on September 28, 2009 to provide targeted
liability protections for pandemic countermeasures to enhance
distribution and to add provisions consistent with other declarations,
and republished the declaration each time in its entirety;
Whereas, the September 28, 2009 declaration extended through
February 28, 2010 for vaccines against influenza virus strains named in
the Declaration other than 2009 H1N1 influenza vaccine;
Whereas, modifications are necessary to revise covered
countermeasures and to extend the effective date of the Declaration;
Whereas, the findings I made in the declaration issued on September
28, 2009 continue to apply;
Whereas, in accordance with section 319F-3(b)(6) of the Act (42
U.S.C. 247d-6d(b)), I have considered the desirability of encouraging
the design, development, clinical testing or investigation,
manufacturing, labeling, distribution, formulation, packaging,
marketing, promotion, sale, purchase, donation, dispensing,
prescribing, administration, licensing, and use of additional covered
countermeasures with respect to the category of disease and population
described in sections II and IV of the September 28, 2009 Republished
Declaration, as hereby amended, and have found it desirable to
encourage such activities for these additional covered countermeasures,
and;
Whereas, to encourage the design, development, clinical testing or
investigation, manufacturing and product formulation, labeling,
distribution, packaging, marketing, promotion, sale, purchase,
donation, dispensing, prescribing, administration, licensing, and use
of medical countermeasures with respect to the category of disease and
population described in sections II and IV of the September 28, 2009
Republished Declaration, as hereby amended, it is advisable, in
accordance with section 319F-3(a) and (b) of the Act, to provide
immunity from liability for covered persons, as that term is defined at
section 319F-3(i)(2) of the Act, and to include as such covered persons
other qualified persons as I have identified in section VI of the
September 28, 2009 Republished Declaration, as amended;
Therefore, pursuant to section 319F-3(b) of the Act, I have
determined that there is a credible risk that the spread of influenza A
viruses with pandemic potential and resulting disease could in the
future constitute a public health emergency and that spread of one of
these viruses (2009 H1N1 Influenza) has caused a disease that
constitutes a public health emergency.
In order to extend the scope of covered countermeasures and to
extend the effective date of the Declaration, the September 28, 2009
Republished Declaration, is hereby amended as follows:
In the title, delete ``for H5N1, H2, H6, H7, H9 and 2009 H1N1
Vaccines'' and replace with ``for Vaccines Against Pandemic Influenza A
Viruses and Those with Pandemic Potential''.
In the recitals, delete the first through the fourth ``whereas''
clauses, and insert two new recitals as follows:
Whereas there are or may be multiple animal influenza A viruses
circulating in wild birds and/or domestic animals that cause, or have
significant potential to cause, sporadic human infections or have
mutated to cause pandemics in humans;
Whereas, these viruses may evolve or have evolved into virus
strains capable of causing a pandemic of human influenza because these
viruses may cause infection in, and spread among, humans and because
humans have little or no immunity to these viruses;
In the sixth ``whereas'' clause, insert ``October 1, 2009, and
December 28, 2009'' after ``July 24, 2009''.
In the ``therefore'' clause, delete ``avian influenza viruses and
resulting disease could in the future constitute a public health
emergency, and that 2009 H1N1 influenza constitutes a public health
emergency'' and replace with: ``pandemic influenza A viruses and those
with pandemic potential and resulting disease does or could constitute
a public health emergency''.
In section I, first paragraph, delete ``the pandemic
countermeasures influenza A H5N1, H2, H6, H7, H9, and 2009 H1N1
vaccines'' each time it appears and replace with ``vaccines against
pandemic influenza A viruses with pandemic potential''.
In section I, at the end of the second sentence, replace ``IX''
with ``X''.
In section II, delete ``the virus with (1) highly pathogenic avian
influenza A (H5N1, H2, H6, H7, or H9) virus; or (2) 2009 H1N1
influenza'' and replace with ``animal and/or human influenza A viruses
against which most humans do not have immunity, except those included
in seasonal influenza vaccines and/or covered under the National
Vaccine Injury Compensation Program, that are circulating in wild birds
and/or domestic animals causing or having significant potential to
cause sporadic human infections or have mutated to cause pandemics in
humans''.
In section III, first paragraph, delete in its entirety and replace
with: ``The effective period of time of this Declaration commenced as
described in the September 28, 2009 Republished Declaration, and
extends through February 28, 2012.
In section III, second paragraph, delete ``; except that with
respect to 2009 H1N1 influenza vaccine, the effective period commences
on June 15, 2009 and extends through March 31, 2013'' and replace with
``through February 28, 2012.''
In section III, add to the end of the section as a new paragraph:
``With respect to any covered countermeasure subsequently covered under
the
[[Page 10270]]
National Vaccine Injury Compensation Program, the effective time period
expires immediately upon such coverage.''
In section VIII, insert ``and use'' after ``administration in the
first sentence, delete ``the Act's'' from the second sentence and
replace with ``this'', and delete ``Countermeasure'' from the second
sentence and replace with ``Countermeasures''.
In section IX, add to the end of the first sentence: ``; and
amended on September 28, 2009 to provide targeted liability protections
for pandemic countermeasures to enhance distribution and to add
provisions consistent with other declarations and republished in its
entirety.''
In section X, after the fifth paragraph, insert a new definition as
follows:
Pandemic influenza A viruses and those with pandemic potential:
Animal and/or human influenza A viruses, except those included in
seasonal influenza vaccines and/or covered under the National Vaccine
Injury Compensation Program, that are circulating in wild birds and/or
domestic animals, that cause, or have significant potential to cause,
sporadic or ongoing human infections, or historically have caused
pandemics in humans, or have mutated to cause pandemics in humans, and
for which the majority of the population is immunologically na[iuml]ve.
In Appendix I, title and item 32, add ``H7,'' after ``H6''.
Throughout, insert ``National'' before ``Vaccine Injury
Compensation Fund''.
All other provisions of the June 15, 2009 Republished Declaration
remain in full force.
Republication of HHS Secretary's September 28, 2009 Republished
Declaration, as Amended, for the Use of the Public Readiness and
Emergency Preparedness Act for Vaccines Against Pandemic Influenza A
Viruses and Those with Pandemic Potential.
To the extent any term of the September 28 Republished Declaration,
as hereby amended, is inconsistent with any provision of this
Republished Declaration, the terms of this Republished Declaration are
controlling.
Whereas there are or may be multiple animal influenza A viruses
circulating in wild birds and/or domestic animals that cause, or have
significant potential to cause, sporadic human infections or have
mutated to cause pandemics in humans;
Whereas, these viruses may evolve or have evolved into virus
strains capable of causing a pandemic of human influenza because these
viruses may cause infection in, and spread among, humans and because
humans have little immunity to these viruses;
Whereas, on April 26, 2009, Acting Secretary Charles E. Johnson
determined under section 319 of the Public Health Service Act, (42
U.S.C. 247d), that a public health emergency exists nationwide
involving the Swine Influenza A virus that affects or has significant
potential to affect the national security (now called ``2009-H1N1
influenza'');
Whereas, on July 24, 2009, October 1, 2009, and December 28, 2009 I
renewed the determination by the Acting Secretary that a public health
emergency exists nationwide involving the Swine influenza A virus (now
called ``2009-H1N1 influenza virus'');
Whereas, vaccination may be effective to protect persons from the
threat of pandemic influenza;
Whereas, the possibility of governmental program planners obtaining
stockpiles from private sector entities except through voluntary means
such as commercial sale, donation, or deployment would undermine
national preparedness efforts and should be discouraged as provided for
in section 319F-3(b)(2)(E) of the Public Health Service Act (42 U.S.C.
247d-6d(b)) (``the Act'');
Whereas, immunity under section 319F-3(a) of the Act should be
available to governmental program planners for distributions of Covered
Countermeasures obtained voluntarily, such as by (1) donation; (2)
commercial sale; (3) deployment of Covered Countermeasures from Federal
stockpiles; or (4) deployment of donated, purchased, or otherwise
voluntarily obtained Covered Countermeasures from State, local, or
private stockpiles;
Whereas, the extent of immunity under section 319F-3(a) of the Act
afforded to a governmental program planner that obtains Covered
Countermeasures except through voluntary means is not intended to
affect the extent of immunity afforded other covered persons with
respect to such covered countermeasures;
Whereas, to encourage the design, development, clinical testing or
investigation, manufacturing and product formulation, labeling,
distribution, packaging, marketing, promotion, sale, purchase,
donation, dispensing, prescribing, administration, licensing, and use
of medical countermeasures with respect to the category of disease and
population described in section II and IV it is advisable, in
accordance with section 319F-3(a) and (b) of the Act, to provide
immunity from liability for covered persons, as that term is defined at
section 319F-3(i)(2) of the Act, and to include as such covered persons
such other qualified persons as I have identified in section VI;
Whereas, in accordance with section 319F-3(b)(6) of the Public
Health Service Act (42 U.S.C. 247d-6d(b)) (``the Act''), I have
considered the desirability of encouraging the design, development,
clinical testing or investigation, manufacturing and product
formulation, labeling, distribution, packaging, marketing, promotion,
sale, purchase, donation, dispensing, prescribing, administration,
licensing, and use of medical countermeasures with respect to the
category of disease and population described in sections II and IV
below, and have found it desirable to encourage such activities for the
Covered Countermeasures;
Therefore, pursuant to section 319F-3(b) of the Act, I have
determined there is a credible risk that the spread of pandemic
influenza A viruses and those with pandemic potential and resulting
disease does or could constitute a public health emergency.
I. Covered Countermeasures (as Required by Section 319F-3(b)(1) of the
Act)
Covered Countermeasures are defined at section 319F-3(i) of the
Act.
At this time, and in accordance with the provisions contained
herein, I am recommending the manufacture, testing, development,
distribution, dispensing; and, with respect to the category of disease
and population described in sections II and IV, below, the
administration and usage of vaccines against influenza A viruses with
pandemic potential and any associated adjuvants. The immunity specified
in section 319F-3(a) of the Act shall only be in effect with respect
to: (1) Present or future Federal contracts, cooperative agreements,
grants, interagency agreements, or memoranda of understanding for
vaccines against pandemic influenza A viruses with pandemic potential
used and administered in accordance with this declaration, and (2)
activities authorized in accordance with the public health and medical
response of the Authority Having Jurisdiction to prescribe, administer,
deliver, distribute or dispense the pandemic countermeasures following
a declaration of an emergency, as defined in section X below. In
accordance with section 319F-3(b)(2)(E) of the Act, for governmental
program planners, the immunity specified in section 319F-3(a) of the
Act shall be in effect to the extent they obtain Covered
Countermeasures through voluntary
[[Page 10271]]
means of distribution, such as (1) donation; (2) commercial sale; (3)
deployment of Covered Countermeasures from Federal stockpiles; or (4)
deployment of donated, purchased, or otherwise voluntarily obtained
Covered Countermeasures from State, local, or private stockpiles. For
all other covered persons, including other program planners, the
immunity specified in section 319F-3(a) of the Act shall, in accordance
with section 319F-3(b)(2)(E) of the Act, be in effect pursuant to any
means of distribution.
This Declaration shall subsequently refer to the countermeasures
identified above as Covered Countermeasures.
This Declaration shall apply to all Covered Countermeasures
administered or used during the effective time period of the
Declaration.
II. Category of Disease (as Required by Section 319F-3(b)(2)(A) of the
Act)
The category of disease for which I am recommending the
administration or use of the Covered Countermeasures is the threat of
or actual human influenza that results from the infection of humans
following exposure to animal and/or human influenza A viruses, against
which most humans do not have immunity, except those included in
seasonal influenza vaccines and/or covered under the National Vaccine
Injury Compensation Program, that are circulating in wild birds and/or
domestic animals causing or have significant potential to cause
sporadic human infections or have mutated to cause pandemics in humans.
III. Effective Time Period (as Required by Section 319F-3(b)(2)(B) of
the Act)
The effective period of time of this Declaration commenced as
described in the September 28, 2009 Republished Declaration and extends
through February 28, 2012.
With respect to Covered Countermeasures administered and used in
accordance with the public health and medical response of the Authority
Having Jurisdiction, the effective period of time of this Declaration
commences on the date of a declaration of an emergency and lasts
through and includes the final day that the emergency declaration is in
effect including any extensions thereof through February 28, 2012.
With respect to any covered countermeasure subsequently covered
under the National Vaccine Injury Compensation Program, the effective
time period expires immediately upon such coverage.
IV. Population (as Required by Section 319F-3(b)(2)(C) of the Act)
Section 319F-3(a)(4)(A) confers immunity to manufacturers and
distributors of the Covered Countermeasure, regardless of the defined
population.
Section 319F-3(a)(3)(C)(i) confers immunity to covered persons who
could be program planners or qualified persons with respect to the
Covered Countermeasure only if a member of the population specified in
the Declaration administers or uses the Covered Countermeasure and is
in or connected to the geographic location specified in this
Declaration, or the program planner or qualified person reasonably
could have believed that these conditions were met.
The populations specified in this Declaration are the following:
(1) All persons who use a Covered Countermeasure or to whom such a
Covered Countermeasure is administered as an Investigational New Drug
in a human clinical trial conducted directly by the Federal Government,
or pursuant to a contract, grant or cooperative agreement with the
Federal Government; (2) all persons who use a Covered Countermeasure or
to whom such a Countermeasure is administered in a pre-pandemic phase,
as defined below; and/or (3) all persons who use a Covered
Countermeasure, or to whom such a Covered Countermeasure is
administered in a pandemic phase, as defined below.
V. Geographic Area (as Required by Section 319F-3(b)(2)(D) of the Act)
Section 319F-3(a) applies to the administration and use of a
Covered Countermeasure without geographic limitation.
VI. Other Qualified Persons (as Required by Section 319F-3(i)(8)(B) of
the Act)
With regard to the administration or use of a Covered
Countermeasure, Section 319F-3(i)(8)(A) of the Act defines the term
``qualified person'' as a licensed individual who is authorized to
prescribe, administer, or dispense the countermeasure under the law of
the State in which such Covered Countermeasure was prescribed,
administered or dispensed. Additional persons who are qualified persons
pursuant to section 319F-3(i)(8)(B) are the following: (1) Any person
authorized in accordance with the public health and medical emergency
response of the Authority Having Jurisdiction to prescribe, administer,
deliver, distribute or dispense Covered Countermeasures, and their
officials, agents, employees, contractors and volunteers, following a
declaration of an emergency, and (2) Any person authorized to
prescribe, administer, or dispense Covered Countermeasures or who is
otherwise authorized under an Emergency Use Authorization.
VII. Additional Time Periods of Coverage After Expiration of
Declaration (as Required by Section 319F-3(b)(3)(B) of the Act)
A. I have determined that, upon expiration of the applicable time
period specified in Section III above, an additional twelve (12) months
is a reasonable period to allow for the manufacturer to arrange for
disposition of the Covered Countermeasure, including the return of such
product to the manufacturer, and for covered persons to take such other
actions as are appropriate to limit the administration or use of the
Covered Countermeasure, and the liability protection of section 319F-
3(a) of the Act shall extend for that period.
B. The Federal Government shall purchase the entire production of
Covered Countermeasures under the contracts specifically listed by
contract number in section I for the stockpile under section 319F-2 of
the Act, and shall be subject to the time-period extension of section
319F-3(b)(3)(C). Production under future contracts for the same vaccine
will also be subject to the time-period extension of section 319F-
3(b)(3)(C).
VIII. Compensation Fund
In addition to conferring immunity to manufacturers, distributors,
and administrators of the Covered Countermeasures, the Act provides
benefits to certain individuals who sustain a covered injury as the
direct result of the administration or use of the Covered
Countermeasure. The Countermeasures Injury Compensation Program (CICP)
within the Health Resources and Services Administration (HRSA)
administers this compensation program. Information about the CICP is
available at 1-888-275-4772 or https://www.hrsa.gov/countermeasurescomp/default.htm.
IX. Amendments
The Declaration for the Use of the Public Readiness and Emergency
Preparedness Act for H5N1 was published on January 26, 2007; amended on
November 30, 2007 to add H7 and H9 vaccines; amended on October 17,
2008 to add H2 and H6 vaccines; amended on June 15, 2009 to add 2009
H1N1 vaccines and
[[Page 10272]]
republished in its entirety; and amended on September 28, 2009 to
provide targeted liability protections for pandemic countermeasures to
enhance distribution and to add provisions consistent with other
declarations and republished in its entirety. This Declaration
incorporates all amendments prior to the date of its publication in the
Federal Register. Any future amendment to this Declaration will be
published in the Federal Register, pursuant to section 319F-2(b)(4) of
the Act.
X. Definitions
For the purpose of this Declaration, including any claim for loss
brought in accordance with section 319F-3 of the PHS Act against any
covered persons defined in the Act or this Declaration, the following
definitions will be used:
Administration of a Covered Countermeasure: As used in section
319F-3(a)(2)(B) of the Act includes, but is not limited to, public and
private delivery, distribution, and dispensing activities relating to
physical administration of the countermeasures to recipients,
management and operation of delivery systems, and management and
operation of distribution and dispensing locations.
Authority Having Jurisdiction: Means the public agency or its
delegate that has legal responsibility and authority for responding to
an incident, based on political or geographical (e.g., city, county,
Tribal, State, or Federal boundary lines) or functional (e.g., law
enforcement, public health) range or sphere of authority.
Covered Persons: As defined at section 319F-3(i)(2) of the Act,
include the United States, manufacturers, distributors, program
planners, and qualified persons. The terms ``manufacturer,''
``distributor,'' ``program planner,'' and ``qualified person'' are
further defined at sections 319F-3(i)(3), (4), (6), and (8) of the Act.
Declaration of Emergency: A declaration by any authorized local,
regional, State, or Federal official of an emergency specific to events
that indicate an immediate need to administer and use pandemic
countermeasures, with the exception of a Federal declaration in support
of an emergency use authorization under section 564 of the FDCA unless
such declaration specifies otherwise.
Pandemic influenza A viruses and those with pandemic potential:
Animal and/or human influenza A viruses, except those included in
seasonal influenza vaccines and/or covered under the National Vaccine
Injury Compensation Program, that are circulating in wild birds and/or
domestic animals, that cause, or have significant potential to cause,
sporadic or ongoing human infections, or historically have caused
pandemics in humans, or have mutated to cause pandemics in humans, and
for which the majority of the population is immunologically na[iuml]ve.
Pandemic Phase: The following stages, as defined in the National
Strategy for Pandemic Influenza: Implementation Plan (Homeland Security
Council, May 2006): (4) First Human Case in North America; and (5)
Spread Throughout United States.
Pre-pandemic Phase: The following stages, as defined in the
National Strategy for Pandemic Influenza: Implementation Plan (Homeland
Security Council, May 2006): (0) New Domestic Animal Outbreak in At-
Risk Country; (1) Suspected Human Outbreak Overseas; (2) Confirmed
Human Outbreak Overseas; and (3) Widespread Human Outbreaks in Multiple
Locations Overseas.
Dated: February 26, 2010.
Kathleen Sebelius,
Secretary.
APPENDIX
I. List of U.S. Government Contracts--Covered H5N1, H2, H6, H7, H9, and
2009-H1N1 Vaccine Contracts
1. HHSN266200400031C
2. HHSN266200400032C
3. HHSN266200300039C
4. HHSN266200400045C
5. HHSN266200205459C
6. HHSN266200205460C
7. HHSN266200205461C
8. HHSN266200205462C
9. HHSN266200205463C
10. HHSN266200205464C
11. HHSN266200205465C
12. HHSN266199905357C
13. HHSN266200300068C
14. HHSN266200005413C
15. HHSO100200600021C (formerly 200200409981)
16. HHSO100200500004C
17. HHSO100200500005I
18. HHSO100200700026I
19. HHSO100200700027I
20. HHSO100200700028I
21. HHSO100200600010C
22. HHSO100200600011C
23. HHSO100200600012C
24. HHSO100200600013C
25. HHSO100200600014C
26. HHSO100200600022C (formerly 200200511758)
27. HHSO100200600023C (formerly 200200410431)
28. CRADA No. AI-0155 NIAID/MedImmune
29. HHSO100200700029C
30. HHSO100200700030C
31. HHSO100200700031C
32. All present, completed and future Government H5N1, H2, H6, H7,
H9, and 2009-H1N1 vaccine contracts not otherwise listed.
[FR Doc. 2010-4644 Filed 3-4-10; 8:45 am]
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