[Congressional Bills 117th Congress]
[From the U.S. Government Publishing Office]
[S. 3395 Introduced in Senate (IS)]
<DOC>
117th CONGRESS
1st Session
S. 3395
To amend the Federal Food, Drug, and Cosmetic Act with respect to
records and other information inspections.
_______________________________________________________________________
IN THE SENATE OF THE UNITED STATES
December 14, 2021
Ms. Baldwin (for herself and Mr. Cassidy) introduced the following
bill; which was read twice and referred to the Committee on Health,
Education, Labor, and Pensions
_______________________________________________________________________
A BILL
To amend the Federal Food, Drug, and Cosmetic Act with respect to
records and other information inspections.
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 ``Medical Device Integrity Act''.
SEC. 2. RECORDS AND OTHER INFORMATION INSPECTION.
(a) In General.--Section 704(a)(4)(A) of the Federal Food, Drug,
and Cosmetic Act (21 U.S.C. 374(a)(4)(A)) is amended--
(1) in the first sentence, by inserting ``or device'' after
``processing of a drug''; and
(2) in the second sentence, by striking ``shall include''
and all that follows through the period at the end and
inserting the following: ``shall include--
``(A) a sufficient description of the records
requested; and
``(B) a rationale for requesting such information
in advance of, or in lieu of, an inspection.''.
(b) Guidance.--Not later than 1 year after the date of enactment of
this Act, the Secretary shall issue draft guidance describing the
circumstances in which the Secretary intends to issue requests for
records or other information in advance of, or in lieu of, an
inspection, processes for responding to such requests electronically or
in physical form, and factors the Secretary intends to consider in
evaluating whether such records are provided within a reasonable
timeframe, within reasonable limits, and in a reasonable manner,
accounting for resource and other limitations that may exist, including
for small businesses. The Secretary shall issue final guidance not
later than 1 year after the close of the comment period for the draft
guidance.
<all>