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Zdrowie i gospodarka · 4.08.1998

Agency Information Collection Activities: Proposed Collection; Comment Request

The Food and Drug Administration (FDA) is announcing an opportunity for public comment on the proposed collection of certain information by the agency. Under the Paperwork Reduction Act of 1995 (the PRA), Federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the Third-Party Review Pilot Program established by FDA's Center for Devices and Radiological Health (CDRH) under the FDA Modernization Act of 1997 (FDAMA). Elsewhere in this issue of the Federal Register, FDA is publishing a notice announcing OMB's approval of this collection of information (OMB control number 0910-0375). Since this was an emergency approval that expires on November 30, 1998, FDA is following the normal PRA clearance procedures by isuing this notice.

Source: Federal Register — Food and Drug AdministrationOpen original release →