[Congressional Bills 114th Congress]
[From the U.S. Government Publishing Office]
[H.R. 2423 Introduced in House (IH)]
114th CONGRESS
1st Session
H. R. 2423
To amend the Federal Food, Drug, and Cosmetic Act with respect to valid
scientific evidence.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
May 19, 2015
Mr. Shimkus introduced the following bill; which was referred to the
Committee on Energy and Commerce
_______________________________________________________________________
A BILL
To amend the Federal Food, Drug, and Cosmetic Act with respect to valid
scientific evidence.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. VALID SCIENTIFIC EVIDENCE.
Section 513(a)(3)(B) of the Federal Food, Drug, and Cosmetic Act
(21 U.S.C. 360c(a)(3)(B)) is amended--
(1) by redesignating clauses (i) and (ii) as subclauses (I)
and (II), respectively;
(2) by striking ``(B) If the Secretary'' and inserting
``(B)(i) If the Secretary''; and
(3) by adding at the end the following:
``(ii) Valid scientific evidence for purposes of
clause (i) may include:
``(I) evidence described in well-documented
case histories, including registry data, that
are collected and monitored under an acceptable
protocol;
``(II) studies published in peer-reviewed
journals; and
``(III) data collected in countries other
than the United States so long as such data
otherwise meets the criteria specified in this
subparagraph.
``(iii) In the case of a study published in a peer-
reviewed journal that is offered as valid scientific
evidence for purposes of clause (i), the Secretary may
request data underlying the study if--
``(I) the Secretary, in making such
request, complies with the requirement of
subparagraph (D)(ii) to consider the least
burdensome appropriate means of evaluating
device effectiveness or subsection (i)(1)(D) to
consider the least burdensome means of
determining substantial equivalence, as
applicable;
``(II) the Secretary furnishes a written
rationale for so requesting the underlying data
together with such request; and
``(III) if the requested underlying data
for such a study are unavailable, the Secretary
shall consider such study to be part of the
totality of the evidence with respect to the
device, as the Secretary determines
appropriate.''.
<all>