EXECUTIVE OFFICE OF THE PRESIDENT OFFICE OF MANAGEMENT AND BUDGET WASHINGTON, D.C. 20503
STATEMENT OF ADMINISTRATION POLICY (THIS STATEMENT HAS BEEN COORDINATED BY OMB WITH THE CONCERNED AGENCIES.)
September 24, 1997
S. 830 - FDA Modernization and Accountability Act of 1997
(Sen. Jeffords (R) VT)
The Administration applauds the Senate for its bipartisan effort to improve S.
830 since it was reported by the Senate Committee on Labor and Human Resources,
and appreciates the Senate's responsiveness to concerns that have been
raised. Because of the importance of obtaining a five-year extension of the
Prescription Drug User Fee Act (PDUFA), the Administration has no objection to
passage of the bill by the Senate at this time. However, the Administration
finds that the provisions identified below are unacceptable and as the
legislative process continues, will work to ensure that our remaining concerns
In general, this legislation represents a significant step toward accomplishing
our mutual goal of assuring the agency's optimum performance while protecting
the health of the American public. The Administration, however, continues to
have two major concerns with the bill.
First, section 404 of the bill would lower the review standard for marketing
approval by precluding the Food and Drug Administration (FDA) from reviewing
new medical devices for uses other than those for which the manufacturer says
they are intended. Second, the PDUFA trigger as proposed in S. 830 undercuts
the bipartisan budget agreement (BBA) by requiring budget increases for FDA not
envisioned by the BBA, and would interfere with HHS' ability to allocate
resources appropriately throughout the Department.
In order to be able to support the final bill, the Administration will continue
to work with the House of Representatives and in conference to resolve these
and other identified issues.