Book Detail
Edition:
Release: 2012-07-06
Publisher: CreateSpace Independent Publishing Platform
Binding: Paperback
ISBN/ASIN: 1478201452
Format: hardcover, kindle, PDF, EPUB
The FDA Medical Device User Fee Program pdf
Description
On June 20, 2012, the House of Representatives passed, by voice vote and under suspension of the rules, S. 3187 (EAH), the Food and Drug Administration Safety and Innovation Act, as amended. This bill would reauthorize the FDA prescription drug and medical device user fee programs (which would otherwise expire on September 30, 2012), create new user fee programs for generic and biosimilar drug approvals, and make other revisions to other FDA drug and device approval processes. It reflects bicameral compromise on earlier versions of the bill (S. 3187 [ES], which passed the Senate on May 24, 2012, and H.R. 5651 [EH], which passed the House on May 30, 2012). The following CRS reports provide overview information on FDA’s processes for approval and regulation of drugs: CRS Report R41983, How FDA Approves Drugs and Regulates Their Safety and Effectiveness, by Susan Thaul; CRS Report RL33986, FDA’s Authority to Ensure That Drugs Prescribed to Children Are Safe and Effective, by Susan Tha Download The FDA Medical Device User Fee Program for free via rapidshare, mediafire, 4shared, dropBox, uploading, fileserve
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