Review of fast-track extension request submitted by the administration hearing before the Committee on Agriculture, House of Representatives, One Hundred Second Congress, first session, March 13, 1991. by United States. Congress. House. Committee on Agriculture

Cover of: Review of fast-track extension request submitted by the administration | United States. Congress. House. Committee on Agriculture

Published by [U.S. G.P.O.], For sale by the U.S. G.P.O., Supt. of Docs., Congressional Sales Office in Washington, DC .

Written in English

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Places:

  • United States,
  • Mexico,
  • United States.,
  • Mexico.

Subjects:

  • Canada.,
  • Free trade -- United States.,
  • Agriculture -- Economic aspects -- United States.,
  • Produce trade -- United States.,
  • Exports -- United States.,
  • Free trade -- Mexico.,
  • United States -- Foreign economic relations -- Mexico.,
  • Mexico -- Foreign economic relations -- United States.

Edition Notes

Book details

Other titlesReview of fast track extension request submitted by the administration.
Classifications
LC ClassificationsKF27 .A3 1991a
The Physical Object
Paginationiv, 222 p. ;
Number of Pages222
ID Numbers
Open LibraryOL1666929M
ISBN 100160353173
LC Control Number91601502
OCLC/WorldCa24392696

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Congress. House. Committee on Agriculture.]. Fast track journals are crucial for research articles that are exceptionally important and requires urgent dissemination, or where there is a funding policy reason for urgent publication. AIJR offers faster review for such articles within 3 days to weeks of submission and if accepted will get published within 3 days of acceptance.

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Authors. The Agency estimates the total annual number of respondents submitting requests for fast track designation is approximatelyand the number of requests received is approximately annually. FDA estimates that the number of hours needed to prepare a request for fast track designation is approximately 60 hours per request (row 3 in table 1).

the use of its Fast Track and Priority Review programs provide the review times for successful applications. Table 2 compares the review times, by year and type of review procedure, for all approved NDA/BLAs applications that were submitted from FY through FYFile Size: 77KB.

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Request for extension of approval. SUMMARY: The Indian Health Service (IHS), as part of its continuing effort to reduce paperwork and respondent burden, invites the general public to take this opportunity to comment on the “Generic Clearance for the Collection of Qualitative Feedback on Agency Service.

Priority review means that FDA will review and act on the application within six months, rather than 10 months under standard review (9, 10). Second, at the request of the sponsor, FDA will designate the QIDP as a fast-track product, which means FDA will facilitate.

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Administration of the Instrument: Identify how the information will be collected. More than one box may be checked. Indicate whether there will be interviewers (e.g. for surveys) or facilitators (e.g., for focus groups) used. Submit all instruments, instructions, and scripts are submitted with the request.

The Need for Fast Track Authority It is past time for the President and Congress to agree on a formula for fast-track extension and end this very bad situation. The point is that administration should make a case for what negotiations it wants to be free to initiate under fast track, and Congress should review that case and decide.

The fast track authority for brokering trade agreements is the authority of the President of the United States to negotiate international agreements that Congress can approve or deny but cannot amend or d the trade promotion authority (TPA) infast track negotiating authority is an impermanent power granted by Congress to the President.

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T/F: In addition, an application for a drug designated as a Qualified Infectious Disease Products QIDP is eligible for Priority Review and Fast Track designation. Priority review is a program of the United States Food and Drug Administration (FDA) to expedite the review process for drugs that are expected to have a particularly great impact on the treatment of a disease.

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