HR 3812 IH
106th CONGRESS
2d Session
H. R. 3812
To create incentives for private sector research related to
developing vaccines against widespread diseases and ensure that such vaccines
are affordable and widely distributed.
IN THE HOUSE OF REPRESENTATIVES
March 1, 2000
Ms. PELOSI (for herself, Mr. LANTOS, Mr. INSLEE, Mr. HINCHEY, Mr. JEFFERSON,
Mr. JACKSON of Illinois, Ms. WOOLSEY, Mr. MATSUI, Mrs. MORELLA, and Mr.
ROMERO-BARCELO) introduced the following bill; which was referred to the
Committee on Ways and Means, and in addition to the Committees on International
Relations, and Commerce, for a period to be subsequently determined by the
Speaker, in each case for consideration of such provisions as fall within the
jurisdiction of the committee concerned
A BILL
To create incentives for private sector research related to
developing vaccines against widespread diseases and ensure that such vaccines
are affordable and widely distributed.
Be it enacted by the Senate and House of Representatives of the United
States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the `Vaccines for the New Millennium Act of
2000'.
SEC. 2. FINDINGS.
Congress finds the following:
(1) Vaccines are among the most cost-effective weapons in the arsenal of
modern medicine to stop the spread of contagious diseases and strengthen an
individual's immune system to resist a wide range of infectious diseases,
and vaccines offer a relatively inexpensive means of lowering a society's
overall cost of medical care.
(2) Every year, up to 3,000,000 children's lives are saved as the result
of early childhood immunizations. But almost 3,000,000 more lives worldwide
are lost from diseases that could be prevented with existing vaccines.
(3) Today, 1 in 4 children do not receive the 6 basic vaccinations:
polio, diptheria, whooping cough, tetanus, measles, and tuberculosis. The
proportion of children immunized against these 6 diseases has declined in
recent years, from approximately 80 percent in 1990 to 74 percent in
1998.
(4) Safe, effective, and universal immunization is a means to end the
tragedy of avoidable childhood deaths, and a means to improve the overall
health, productivity, and security of society.
(5) As well as the challenges of increasing access to existing vaccines,
there are additional challenges for research and development of new
vaccines. Over 5,000,000 people die annually from HIV, tuberculosis, and
malaria. Vaccines against these infectious diseases are urgently
needed.
(6) The spread of HIV is a human tragedy that is reversing previous
gains in life expectancy and exacerbating poverty in developing countries.
Over 33,000,000 people are infected with HIV, and the disease will kill more
than 2,500,000 people this year. More than 11,000,000 children worldwide
have been orphaned by AIDS and 16,000 people become newly infected every
day.
(7) While an estimated $2,000,000,000 is spent annually on research for
AIDS treatment, much of it by the private sector, the total global research
and development for preventive HIV vaccines is substantially less, perhaps
as little as $300,000,000, and of the amount spent on lifesaving vaccine
research, only a fraction is financed by private sector drug
manufacturers.
(8) Between 7,000,000 and 8,000,000 individuals develop active
tuberculosis every year and 2,000,000 to 3,000,000 individuals die from
tuberculosis each year, with tuberculosis accounting for more than 1/4 of
all preventable adult deaths in developing countries. An individual is newly
infected with tuberculosis every second, and someone dies of tuberculosis
every 10 seconds.
(9) Each year, 300,000,000 to 500,000,000 individuals become ill with
malaria, and approximately 1,000,000 individuals die from the disease,
exacting an enormous toll in lives, medical costs, and lost productivity.
The majority of those who die from malaria are children under the age of 5.
One person dies from malaria every 30 seconds.
(10) While additional public funds for basic research are critical in
the effort to find vaccines for HIV, malaria, and tuberculosis, equally
important is a concerted effort by private sector drug manufacturers to find
vaccines for these 3 major infectious diseases.
(11) Additional, targeted public subsidies for private sector lifesaving
vaccine research and development are justified on the basis that achieving
effective and affordable vaccines for HIV, malaria,
and tuberculosis will yield public benefits beyond those benefits captured by
the manufacturer.
SEC. 3. UNIVERSAL EARLY CHILDHOOD IMMUNIZATIONS.
Section 104(c)(3) of the Foreign Assistance Act of 1961 (22 U.S.C.
2151b(c)(3)) is amended in the fourth sentence by striking `the protection of'
and all that follows through `1991' and inserting `the universal protection of
all children from immunizable diseases by December 31, 2009'.
SEC. 4. VOLUNTARY CONTRIBUTION TO GLOBAL ALLIANCE FOR VACCINES AND
IMMUNIZATIONS AND INTERNATIONAL AIDS VACCINE INITIATIVE.
(a) AUTHORIZATION OF APPROPRIATIONS- Section 302 of the Foreign Assistance
Act of 1961 (22 U.S.C. 2222) is amended by adding at the end the following:
`(j) In addition to amounts otherwise available under this section, there
are authorized to be appropriated to the President for fiscal year 2001 an
amount not in excess of $50,000,000 and for fiscal year 2002 an amount not in
excess of $100,000,000 to be available only for United States contributions to
the Global Alliance for Vaccines and Immunizations.
`(k) In addition to amounts otherwise available under this section, there
are authorized to be appropriated to the President for fiscal year 2001
$10,000,000 and for fiscal year 2002 $20,000,000 to be available only for
United States contributions to the International AIDS Vaccine Initiative.'.
(b) REPORT- The President shall include in the July 1 report submitted to
Congress under section 305(b)(1) of the Foreign Assistance Act of 1961 (22
U.S.C. 2226(b)(1)) for fiscal years 2001 and 2002 a report on the
effectiveness of the Global Alliance for Vaccines and Immunizations in meeting
the goals of--
(1) improving access to sustainable immunization services;
(2) expanding the use of all existing, safe, and cost-effective vaccines
where they address a public health problem;
(3) accelerating the development and introduction of new vaccines and
technologies;
(4) accelerating research and development efforts for vaccines needed
primarily in developing countries; and
(5) making immunization coverage a centerpiece in international
development efforts.
SEC. 5. CREDIT FOR MEDICAL RESEARCH RELATED TO DEVELOPING VACCINES AGAINST
WIDESPREAD DISEASES.
(a) IN GENERAL- Subpart D of part IV of subchapter A of chapter 1 of the
Internal Revenue Code of 1986 (relating to business related credits) is
amended by adding at the end the following new section:
`SEC. 45D. CREDIT FOR MEDICAL RESEARCH RELATED TO DEVELOPING VACCINES
AGAINST WIDESPREAD DISEASES.
`(a) GENERAL RULE- For purposes of section 38, the vaccine research credit
determined under this section for the taxable year is an amount equal to 30
percent of the qualified vaccine research expenses for the taxable year.
`(b) QUALIFIED VACCINE RESEARCH EXPENSES- For purposes of this
section--
`(1) QUALIFIED VACCINE RESEARCH EXPENSES-
`(A) IN GENERAL- Except as otherwise provided in this paragraph, the
term `qualified vaccine research expenses' means the amounts which are
paid or incurred by the taxpayer during the taxable year which would be
described in subsection (b) of section 41 if such subsection were applied
with the modifications set forth in subparagraph (B).
`(B) MODIFICATIONS- For purposes of subparagraph (A), subsection (b)
of section 41 shall be applied--
`(i) by substituting `vaccine research' for `qualified research'
each place it appears in paragraphs (2) and (3) of such subsection,
and
`(ii) by substituting `75 percent' for `65 percent' in paragraph
(3)(A) of such subsection.
`(C) EXCLUSION FOR AMOUNTS FUNDED BY GRANTS, ETC- The term `qualified
vaccine research expenses' shall not include any amount to the extent such
amount is funded by any grant, contract, or otherwise by another person
(or any governmental entity).
`(2) VACCINE RESEARCH- The term `vaccine research' means research to
develop vaccines and microbicides for--
`(D) any infectious disease (of a single etiology) which, according to
the World Health Organization, causes over 1,000,000 human deaths
annually.
`(c) COORDINATION WITH CREDIT FOR INCREASING RESEARCH EXPENDITURES-
`(1) IN GENERAL- Except as provided in paragraph (2), any qualified
vaccine research expenses for a taxable year to which an election under this
section applies shall not be taken into account for purposes of determining
the credit allowable under section 41 for such taxable year.
`(2) EXPENSES INCLUDED IN DETERMINING BASE PERIOD RESEARCH EXPENSES- Any
qualified vaccine research expenses for any taxable year which are qualified
research expenses (within the meaning of section 41(b)) shall be taken into
account in determining base period research expenses for purposes of
applying section 41 to subsequent taxable years.
`(1) LIMITATIONS ON FOREIGN TESTING- No credit shall be allowed under
this section with respect to any vaccine research (other than human clinical
testing) conducted outside the United States.
`(2) CERTAIN RULES MADE APPLICABLE- Rules similar to the rules of
paragraphs (1) and (2) of section 41(f) shall apply for purposes of this
section.
`(3) ELECTION- This section (other than subsection (e)) shall apply to
any taxpayer for any taxable year only if such taxpayer elects to have this
section apply for such taxable year.
`(e) SHAREHOLDER EQUITY INVESTMENT CREDIT IN LIEU OF RESEARCH CREDIT-
`(1) IN GENERAL- For purposes of section 38, the vaccine research credit
determined under this section for the taxable year shall include an amount
equal to 20 percent of the amount paid by the taxpayer to acquire qualified
research stock in a corporation if--
`(A) the amount received by the corporation for such stock is used
within 18 months after the amount is received to pay qualified vaccine
research expenses of the corporation for which a credit would (but for
subparagraph (B) and subsection (d)(3)) be determined under this section,
and
`(B) the corporation waives its right to the credit determined under
this section for the qualified vaccine research expenses which are paid
with such amount.
`(2) QUALIFIED RESEARCH STOCK- For purposes of paragraph (1), the term
`qualified research stock' means any stock in a C corporation--
`(A) which is originally issued after the date of the enactment of the
Lifesaving Vaccine Technology Act of 1999,
`(B) which is acquired by the taxpayer at its original issue (directly
or through an underwriter) in exchange for money or other property (not
including stock), and
`(C) as of the date of issuance, such corporation meets the gross
assets tests of subparagraphs (A) and (B) of section 1202(d)(1).'
(b) INCLUSION IN GENERAL BUSINESS CREDIT-
(1) IN GENERAL- Section 38(b) of such Code is amended by striking `plus'
at the end of paragraph (11), by striking the period at the end of paragraph
(12) and inserting `, plus', and by adding at the end the following new
paragraph:
`(13) the vaccine research credit determined under section 45D.'.
(2) TRANSITION RULE- Section 39(d) of such Code is amended by adding at
the end the following new paragraph:
`(9) NO CARRYBACK OF SECTION 45D CREDIT BEFORE ENACTMENT- No portion of
the unused business credit for any taxable year which is attributable to the
vaccine research credit determined under section 45D may be carried back to
a taxable year ending before the date of the enactment of section
45D.'.
(c) DENIAL OF DOUBLE BENEFIT- Section 280C of such Code is amended by
adding at the end the following new subsection:
`(d) CREDIT FOR QUALIFIED VACCINE RESEARCH EXPENSES-
`(1) IN GENERAL- No deduction shall be allowed for that portion of the
qualified vaccine research expenses (as defined in section 45D(b)) otherwise
allowable as a deduction for the taxable year which is equal to the amount
of the credit determined for such taxable year under section 45D(a).
`(2) CERTAIN RULES TO APPLY- Rules similar to the rules of paragraphs
(2), (3), and (4) of subsection (c) shall apply for purposes of this
subsection.'.
(d) DEDUCTION FOR UNUSED PORTION OF CREDIT- Section 196(c) of such Code
(defining qualified business credits) is amended by striking `and' at the end
of paragraph (7), by striking the period at the end of paragraph (8) and
inserting `, and', and by adding at the end the following new paragraph:
`(9) the vaccine research credit determined under section 45D(a) (other
than such credit determined under the rules of section 280C(d)(2)).'.
(e) CLERICAL AMENDMENT- The table of sections for subpart D of part IV of
subchapter A of chapter 1 of such Code is amended by adding at the end the
following new item:
`Sec. 45D. Credit for medical research related to developing vaccines against
widespread diseases.'.
(f) EFFECTIVE DATE- The amendments made by this section shall apply to
taxable years ending after the date of the enactment of this Act.
(g) DISTRIBUTION OF VACCINES DEVELOPED USING CREDIT- It is the sense of
the Congress that if credit is allowed under section 45D of the Internal
Revenue Code of 1986 to any corporation or shareholder of a corporation by
reason of vaccine research expenses incurred by the corporation in the
development of a vaccine, such corporation should certify to the Secretary of
the Treasury that, within 1 year after that vaccine is first licensed, such
corporation will establish a good faith plan utilizing technology transfer,
differential pricing, in-country production, or other mechanisms to maximize
international access to high quality and affordable vaccines. The preceding
sentence shall not be construed to waive rights to set prices, patent
ownership, or confidentiality of privileged information.
(h) STUDY- The Institute of Medicine shall conduct a study of the
effectiveness of the credit under section 45D of the Internal Revenue Code of
1986 in stimulating vaccine research. Not later than the date which is 5 years
after the date of the enactment of this Act, the Institute of Medicine shall
submit to the Congress the results of such study together with any
recommendations it may have to improve the effectiveness of such credit in
stimulating vaccine research.
SEC. 6. CREDIT FOR CERTAIN SALES OF LIFESAVING VACCINES.
(a) IN GENERAL- Subpart D of part IV of subchapter A of chapter 1 of the
Internal Revenue Code of 1986 (relating to business related credits), as
amended by section 5(a), is amended by adding at the end the following new
section:
`SEC. 45E. CREDIT FOR CERTAIN SALES OF LIFESAVING VACCINES.
`(a) IN GENERAL- For purposes of section 38, the lifesaving vaccine sale
credit determined under this section with respect to a taxpayer for the
taxable year is an amount equal to the amount of qualified vaccine sales for
the taxable year.
`(b) QUALIFIED VACCINE SALES- For purposes of this section--
`(1) IN GENERAL- The term `qualified vaccine sales' means the aggregate
amount paid to the taxpayer for a qualified sale.
`(A) IN GENERAL- The term `qualified sale' means a sale of a qualified
vaccine--
`(i) to a nonprofit organization, governmental unit, or government
of any foreign government, and
`(ii) for distribution in a developing country.
`(B) DEVELOPING COUNTRY- For purposes of this paragraph, the term
`developing country' means a country which the International Bank for
Reconstruction and Development (commonly referred to as the `World Bank')
determines to be a country with a lower middle income or less.
`(3) QUALIFIED VACCINE- The term `qualified vaccine' means a vaccine (as
defined in section 4132(a)(2)) which is--
`(A) approved by the Food and Drug Administration as a new drug after
the date of the enactment of this paragraph, and
`(iv) any infectious disease (of a single etiology) that is
determined by the Secretary of Health and Human Services (after
consultation with the Director of the Center for Disease Control and
Prevention and the United States Agency for International Development)
to cause the deaths of over 1,000,000 people worldwide each
year.
`(c) LIMIT ON AMOUNT OF CREDIT- The maximum amount of the credit allowable
under subsection (a) with respect to a sale shall not exceed the portion of
the limitation amount allocated under subsection (d) with respect to such
sale.
`(d) NATIONAL LIMITATION ON AMOUNT OF CREDITS-
`(1) IN GENERAL- Except as provided in paragraph (3), there is a
lifesaving vaccine sale credit for each calendar year equal to--
`(A) $100,000,000 for each of years 2002 through 2006,
`(B) $125,000,000 for each of years 2007 through 2010, and
`(2) Allocation of limitation-
`(A) IN GENERAL- The limitation amount under paragraph (1) shall be
allocated on a competitive basis for any calendar year by the Secretary
(in consultation with the Administrator of the United States Agency for
International Development) among organizations with an approved
application.
`(B) APPROVED APPLICATION- For purposes of subparagraph (A), the term
`approved application' means an application which is approved by the
Administrator of the United States Agency for International Development
with respect to a qualified sale made during the calendar year. Such
application shall be made at such time and in such form and manner as the
Administrator shall prescribe by regulation and shall include a detailed
and cost-effective plan for distribution of the vaccine.
`(3) CARRYOVER OF UNUSED LIMITATION- If the limitation amount under
paragraph (1) for any calendar year exceeds the aggregate amount allocated
under paragraph (2), such limitation for the following calendar year shall
be increased by the amount of such excess. The limitation amount shall
remain available until expended.
`(e) SPECIAL RULES- For purposes of this section, rules similar to the
rules of section 41(f)(2) shall apply.'.
(b) INCLUSION IN GENERAL BUSINESS CREDIT-
(1) IN GENERAL- Section 38(b) of the Internal Revenue Code of 1986
(relating to current year business credit), as amended by section 5(b)(1),
is amended by striking `plus' at the end of paragraph (12), by striking the
period at the end of paragraph (13) and inserting `, plus', and by adding at
the end the following new paragraph:
`(14) the lifesaving vaccine sale credit determined under section
45E.'.
(2) TRANSITION RULE- Section 39(d) of such Code (relating to
transitional rules), as amended by section 5(b)(2), is amended by adding at
the end the following new paragraph:
`(10) NO CARRYBACK OF SECTION 45E CREDIT BEFORE ENACTMENT- No portion of
the unused business credit for any taxable year which is attributable to the
lifesaving vaccine sale credit determined under section 45E may be carried
back to a taxable year ending before the date of the enactment of section
45E.'.
(c) CLERICAL AMENDMENT- The table of sections for subpart D of part IV of
subchapter A of chapter 1 of the Internal Revenue Code of 1986, as amended by
section 5(e), is amended by adding at the end the following new item:
`Sec. 45E. Credit for certain sales of lifesaving vaccines.'.
(d) EFFECTIVE DATE- The amendments made by this section shall apply to
sales of vaccines in taxable years beginning after December 31, 2000.
SEC. 7. LIFESAVING VACCINE PURCHASE FUND.
(a) PURPOSE- It is the purpose of this section to--
(1) create incentives for private sector research into vaccines for HIV,
malaria, tuberculosis, and other major infectious diseases; and
(2) ensure that vaccines for major infectious diseases are affordable
and widely distributed.
(b) DEFINITIONS- In this section:
(1) DEVELOPING COUNTRY- The term `developing country' means a country
which the International Bank for Reconstruction and Development (commonly
referred to as the `World Bank') determines to be a country with a lower
middle income or less.
(2) ELIGIBLE VACCINE- The term `eligible vaccine' has the meaning given
the term `qualified vaccine' in section 45E(b)(3) of the Internal Revenue
Code of 1986.
(c) ESTABLISHMENT OF TRUST FUND- There is established in the Treasury of
the United States a trust fund to be known as the `Lifesaving Vaccine Purchase
Fund' (in this section referred to as the `Fund') consisting of amounts
appropriated under subsection (f).
(d) INVESTMENT OF FUND- Amounts in the Fund shall be invested in
accordance with section 9702 of title 31, United States Code, and any interest
on, and proceeds from any such investment shall be credited to and become part
of the Fund.
(1) IN GENERAL- The Secretary of the Treasury (in this section referred
to as the `Secretary') is authorized to expend amounts in the Fund for
purchases of eligible vaccines. Such vaccines shall be distributed to
developing countries.
(2) LIMITATION- The Secretary shall not make expenditures from the Fund
in excess of $100,000,000 for any fiscal year.
(3) REGULATIONS- The Secretary shall promulgate such regulations as are
necessary to carry out the provisions of this subsection, including
regulations regarding--
(A) the procedures for purchasing eligible vaccines, including pricing
rules which take into account the seller's research and development and
manufacturing costs and the desirability of the vaccine purchased, a
funding formula establishing a minimum price per dose, and minimum
technical requirements and a market test requirement for the eligible
vaccine; and
(B) the distribution of eligible vaccines to developing countries
under agreements between the United States Agency for International
Development and international organizations or recipient developing
countries that provide for--
(i) consideration of the prevalence of the disease treated by the
eligible vaccine in the recipient developing country;
(ii) consideration of the ability of the recipient country to
effectively and safely deliver the vaccines; and
(iii) a required matching payment by the recipient developing
country based on the per capita income of the country, in an amount not
in excess of 25 percent of the purchase price paid for such
vaccine.
(4) CONSULTATION- The Secretary shall promulgate regulations under
paragraph (3) after extensive consultation with--
(A) the International Bank for Reconstruction and Development
(commonly referred to as the `World Bank');
(B) the World Health Organization;
(C) the Secretary of Health and Human Services; and
(D) the Lifesaving Vaccine Advisory Commission.
(1) IN GENERAL- Subject to paragraph (2), there are appropriated out of
any funds in the Treasury not otherwise appropriated such sums as may be
necessary to carry out the purposes of the Fund for each of 10 fiscal years
beginning with the first fiscal year in which the Secretary makes an
expenditure from the Fund.
(2) LIMITATION- The amount appropriated for any fiscal year under
paragraph (1) may not exceed $100,000,000.
(3) TRANSFER TO FUND- The Secretary shall transfer the amount
appropriated under paragraph (1) for a fiscal year to the Fund.
(4) AVAILABILITY- Amounts appropriated under this section shall remain
available until expended.
SEC. 8. MULTILATERAL LIFESAVING VACCINE PURCHASE FUND.
(a) NEGOTIATIONS- The President should enter into negotiations with
officials of foreign governments and other interested parties for the
establishment of an international vaccine purchase fund that would--
(1) accept contributions from governments of developed countries;
(2) use such contributions to purchase and distribute in developing
countries vaccines for--
(D) any infectious disease (of a single etiology) which causes the
deaths of over 1,000,000 people worldwide each year; and
(3) be a significant market incentive for private sector vaccine
research.
(b) REPORT- Not later than 1 year after the date of enactment of this Act,
and annually thereafter, the President shall report to Congress on--
(1) the status of negotiations under subsection (a); and
(2) if such fund is established, any recommendations for further action,
including recommendations regarding the Lifesaving Vaccine Purchase Fund
established under section 7 of this Act.
SEC. 9. LIFESAVING VACCINE ADVISORY COMMISSION TO OVERSEE AND EVALUATE
PUBLIC PRIVATE VACCINE PARTNERSHIPS.
(a) ESTABLISHMENT- There is established a commission to be known as the
`Lifesaving Vaccine Advisory
Commission' (referred to in this section as the `Commission').
(1) NUMBER AND APPOINTMENT-
(A) IN GENERAL- The Commission shall be composed of 12 members,
appointed by the President, as follows:
(i) 6 individuals with experience and expertise in the
pharmaceutical or biotechnology industry.
(ii) 6 individuals with experience and expertise in the medical,
public health, or academic community.
The individuals appointed under this subparagraph shall not be
officers or employees of the Federal Government, except to the extent that
they are considered to be such officers or employees by virtue of their
membership on the Commission.
(B) QUALIFICATIONS- The members of the Commission appointed under
subparagraph (A) should, as a group, achieve a balanced membership
representing the Nation as a whole and balancing the concerns of the
public health community with the concerns of the biotechnology and
pharmaceutical industry.
(2) TIME OF APPOINTMENT- Each member of the Commission shall be
appointed not later than 90 days after the date of enactment of this
Act.
(3) TERMS- Each member of the Commission shall be appointed for the life
of the Commission.
(4) VACANCIES- Any vacancy in the Commission shall be filled in the same
manner in which the original appointment was made.
(A) PROHIBITION OF PAY- Except as provided in subparagraph (B),
members of the Commission shall serve without pay.
(B) TRAVEL EXPENSES- Each member of the Commission may receive travel
expenses, including per diem in lieu of subsistence, in accordance with
sections 5702 and 5703 of title 5, United States Code.
(6) QUORUM- 7 members of the Commission shall constitute a quorum.
(7) CHAIRPERSON- The Commission shall select one of the individuals
appointed under paragraph (1) as the chairperson of the Commission.
(8) MEETINGS- The Commission shall meet at the call of its chairperson
or a majority of its members.
(c) DUTIES- The Commission shall--
(1) review the progress of national and international efforts to develop
vaccines for--
(D) any infectious disease (of a single etiology) that is determined
by the Secretary of Health and Human Services (after consultation with the
Director of the Center for Disease Control and Prevention and the
Administrator of the United States Agency for International Development)
to cause the deaths of over 1,000,000 people worldwide each year;
(2) examine the merits of innovative financing mechanisms, such as tax
incentives, purchase funds, patent exchanges, conditional research and
development grants based on market pricing agreements, and other proposals
that combine public subsidies with private sector research and development
efforts, and
(3) develop consensus among industry and public health advocates on
policy recommendations for ways the Federal Government can further advance
public private partnerships, both nationally and internationally, in vaccine
research and development, with a goal of finding effective and affordable
vaccines for the major infectious diseases of the world.
(d) STAFF AND SUPPORT SERVICES-
(A) IN GENERAL- The chairperson of the Commission may, without regard
to civil service laws and regulations and after consultation with the
Commission, appoint an executive director of the Commission and such other
additional personnel as may be necessary to enable the Commission to
perform its duties.
(B) COMPENSATION- The chairperson of the Commission may fix the
compensation of the executive director and other personnel without regard
to the provisions of chapter 51 and subchapter III of chapter 53 of title
5, United States Code, relating to classification of positions and General
Schedule pay rates, except that the rate of pay for the executive director
and other personnel may not exceed the rate
payable for level V of the Executive Schedule under section 5316 of such
title.
(2) STAFF OF FEDERAL AGENCIES- Upon request by the chairperson of the
Commission, the head of any Federal department or agency may detail, on a
nonreimbursable basis, any of the personnel of the department or agency to
the Commission to assist the Commission to carry out its duties under this
Act.
(3) ADMINISTRATIVE SUPPORT SERVICES- The Administrator of General
Services shall provide to the Commission, on a reimbursable basis, any
administrative support services that are necessary to enable the Commission
to carry out this Act.
(e) POWERS OF COMMISSION-
(1) HEARINGS- The Commission may hold such hearings, sit and act at such
times and places, take such testimony, and receive such evidence as the
Commission considers advisable to carry out the purposes of this
section.
(2) INFORMATION FROM FEDERAL AGENCIES- The Commission may secure
directly from any Federal department or agency such information as the
Commission considers necessary to carry out the provisions of this section.
Upon request of the chairperson of the Commission, the head of such
department or agency shall furnish such information to the Commission.
(3) MAILS- The Commission may use the United States mails in the same
manner and under the same conditions as any other Federal agency.
(f) FINAL REPORT- Not later than 18 months after the date of enactment of
this Act, the Commission shall submit to the President and Congress a final
report. The final report shall contain--
(1) a summary of the activities of the Commission;
(2) a final accounting of funds received and expended by the Commission;
and
(3) any findings and recommendations of the Commission which are
supported by at least 9 members.
SEC. 10. SENSE OF CONGRESS.
It is the sense of Congress that flexible or differential pricing for
vaccines, providing lowered prices for the poorest countries, is one of
several valid strategies to accelerate the introduction of vaccines in
developing countries.
END