Home > 106th Congressional Bills > H.R. 3241 (ih) To direct the Secretary of the Interior to recalculate the franchise fee owed by Fort Sumter Tours, Inc., a concessioner providing service to Fort Sumter National Monument in South Carolina, and for other purposes. [Introduced in House] %%F...
H.R. 3241 (ih) To direct the Secretary of the Interior to recalculate the franchise fee owed by Fort Sumter Tours, Inc., a concessioner providing service to Fort Sumter National Monument in South Carolina, and for other purposes. [Introduced in House] %%F...
106th CONGRESS
2d Session
H. R. 3240
_______________________________________________________________________
IN THE SENATE OF THE UNITED STATES
June 29, 2000
Received; read twice and referred to the Committee on Health,
Education, Labor, and Pensions
_______________________________________________________________________
AN ACT
To amend the Federal Food, Drug, and Cosmetic Act to clarify certain
responsibilities of the Food and Drug Administration with respect to
the importation of drugs into the United States.
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 ``Drug Import Fairness Act of 2000''.
SEC. 2. FINDINGS.
The Congress finds as follows:
(1) Pharmacists, patients, and other persons sometimes have
reason to import into the United States drugs that have been
approved by the Food and Drug Administration (``FDA'').
(2) There have been circumstances in which--
(A) a person seeking to import such a drug has
received a notice from FDA that importing the drug
violates or may violate the Federal Food, Drug, and
Cosmetic Act; and
(B) the notice failed to inform the person of the
reasons underlying the decision to send the notice.
(3) FDA should not send a warning notice regarding the
importation of a drug without providing to the person involved
a statement of the underlying reasons for the notice.
SEC. 3. CLARIFICATION OF CERTAIN RESPONSIBILITIES OF FOOD AND DRUG
ADMINISTRATION WITH RESPECT TO IMPORTATION OF DRUGS INTO
UNITED STATES.
Section 801 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C.
381) is amended by adding at the end the following subsection:
``(g)(1) With respect to a drug being imported or offered for
import into the United States, the Secretary may not send a warning
notice to a person (including a pharmacist or wholesale importer)
unless the following conditions are met:
``(A) The notice specifies, as applicable to the
importation of the drug, that the Secretary has made a
determination that--
``(i) importation is in violation of section 801(a)
because the drug is or appears to be adulterated,
misbranded, or in violation of section 505;
``(ii) importation is in violation of section
801(a) because the drug is forbidden or restricted in
sale in the country in which it was produced or from
which it was exported;
``(iii) importation by any person other than the
manufacturer of the drug is in violation of section
801(d); or
``(iv) importation is otherwise in violation of
Federal law.
``(B) The notice does not specify any provision described
in subparagraph (A) that is not applicable to the importation
of the drug.
``(C) The notice states the reasons underlying such
determination by the Secretary, including a brief application
to the principal facts involved of the provision of law
described in subparagraph (A) that is the basis of the
determination by the Secretary.
``(2) The term `warning notice', with respect to the importation of
a drug, means a communication from the Secretary (written or otherwise)
notifying a person, or clearly suggesting to the person, that importing
the drug is, or appears to be, a violation of this Act.''.
Passed the House of Representatives June 29 (legislative
day, June 28), 2000.
Attest:
JEFF TRANDAHL,
Clerk.
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