S.1082 - Medical Device User Fee Amendments of 2007
A bill to amend the Federal Food, Drug, and Cosmetic Act to reauthorize and amend the prescription drug user fee provisions, and for other purposes. view all titles (17)
All Bill Titles
- Short: Medical Device User Fee Amendments of 2007 as reported to senate.
- Short: Pediatric Research Improvement Act as passed senate.
- Official: A bill to amend the Federal Food, Drug, and Cosmetic Act to reauthorize and amend the prescription drug user fee provisions, and for other purposes. as introduced.
- Short: Best Pharmaceuticals for Children Amendments of 2007 as passed senate.
- Short: Domestic Pet Turtle Market Access Act of 2007 as passed senate.
- Short: Medical Device User Fee Amendments of 2007 as passed senate.
- Short: Food and Drug Administration Revitalization Act as reported to senate.
- Short: Best Pharmaceuticals for Children Amendments of 2007 as reported to senate.
- Short: Enhancing Drug Safety and Innovation Act of 2007 as reported to senate.
- Official: An act to amend the Federal Food, Drug, and cosmetic Act and the Public Health Service Act to reauthorize drug and device user fees and ensure the safety of medical products, and for other purposes. as amended by senate.
- Short: Prescription Drug User Fee Amendments of 2007 as introduced.
- Short: Pediatric Medical Device Safety and Improvement Act of 2007 as reported to senate.
- Short: Pediatric Research Improvement Act as reported to senate.
- Short: Food and Drug Administration Revitalization Act as passed senate.
- Short: Enhancing Drug Safety and Innovation Act of 2007 as passed senate.
- Short: Pediatric Medical Device Safety and Improvement Act of 2007 as passed senate.
- Short: Pharmaceutical Market Access and Drug Safety Act of 2007 as passed senate.
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Follow-On Biologics Will Not Make PDUFA, Enzi Spokesman Says
The Senate version of FDARA, S. 1082, contains a placeholder for follow-on biologics legislation, while HR 2900, the House version, does not. ...
Will Follow-On Biologics Bill Become Law?
The two versions of the bills, S. 1082 and HR 2900, are currently pending before a conference committee. The Senate version of the bill contains a ...
Citizen Petition Reforms Under Revised PDUFA to Have Limited Impact
Two versions of the legislation, S. 1082 and HR 2900, are currently pending before a conference committee. Conferees have not been appointed to reconcile ...
Industry Advocate Says Congress, FDA Must Regulate DTC Advertisements
Congress is attempting to regulate DTC advertisements more, such as in S. 1082 and HR 2900, the FDA Revitalization Act, which would give the agency the ...
Security, Detective & Crime : Update on Senate bill S.1082 and ...
(SkyNewswire.com) After enduring numerous amendments, debates and public scrutiny, Senate bill S.1082 is headed for a likely vote on Wednesday, May 9th. ...
Make children's medicines safer
Congress should pass The Food and Drug Revitalization Act of 2007 (S.1082) and The Food and Drug Administration Amendments Act of 2007 (HR 2900) in ...
Pharmacist Group Opposes Legislation to Restrict Compounding
A provision allowing the agency to regulate pharmacies that are mass-compounding drugs should be included in S. 1082 and HR 2900, bills that would enhance ...
Drug Companies Embark Upon Unprecedted Human Experiments
... called the Critical Path Initiative, has recently been endorsed by the birdbrains and gutless cowards that compose the Congress (HR.2900/S.1082). ...
House Set to Vote Today to Allow FDA to Eliminate Vitamin Companies!
The Senate has passed (S. 1082, by a vote of 93-1) legislation which grants the FDA authority to regulate "food and food ingredients. ...
RFID, Bar Codes and Pharmaceutical Authenticity
During the first week of May this year, the US Senate passed the Food and Drug Administration Revitalization Act (S.1082) that included provisions for ...
Legislative update: Pediatric drugs, device legislation debated in ...
The full legislation, known as the Food and Drug Administration Revitalization Act (S. 1082), includes provisions to reauthorize the Best Pharmaceuticals ...
CHINA HAS A SOLUTION FOR THE FDA's PROBLEM
Why did the Senate just pass legislation (S.1082) that gives von Eschenbach significantly more power to do whatever he pleases? And exactly what is it that ...
China sentences ex-head of FDA to death over drug company bribes
Why did the Senate just pass legislation (S.1082) that gives von Eschenbach significantly more power to do whatever he pleases? And exactly what is it that ...
House Democrats Question Financial Incentives For Drug Research In ...
The Senate has approved a measure (S 1082), which the House is considering, that would cut pediatric exclusivity to three months for blockbuster drugs with ...
Sen. Grassley Says FDA Knew Dangers of Avandia, Wants Faster Action
... authority with the Office of New Drugs on these matters when the Senate considered and approved the FDA Revitalization Act (S.1082) earlier this month. ...
House Democrats Question Financial Incentives for Drug Research in ...
The Senate has approved a measure (S 1082), which the House is considering, that would cut pediatric exclusivity to three months for blockbuster drugs with ...
Companies Lobby Against Pediatric Test Provision Of Prescription ...
The Senate version of the bill (S 1082) passed on May 9 included the provision, and Reps. Edward Markey (D-Mass.) and Mike Rogers (R-Mich. ...
World Turtle Day 2007 on Wednesday
The Food and Drug Administration Revitalization Act that recently passed the Senate (S. 1082) included an amendment that would require the FDA to allow the ...
House Panel Considers Reauthorization Of Medical Device User Fees
... timely fashion," but added that "that's not one of the must dos." The Senate passed a PDUFA reauthorization bill (S 1082) on May 9 ( CQ HealthBeat , 5/16).
US Senators financially enslave Americans
... has revealed the apparent financial conflict of interest by US Senators who voted against the infamous S.1082 reimportation amendment. ...
US Senate Bill Proposes Technology to Authenticate Drugs
That act, designed to regulate Internet pharmacies, was a provision rolled into Food and Drug Administration Revitalization Act (S.1082). ...
Companies Lobby Against Pediatric Test Provision of Prescription ...
The Senate version of the bill (S 1082) passed on May 9 included the provision, and Reps. Edward Markey (D-Mass.) and Mike Rogers (R-Mich. ...
Academy Of Managed Care Pharmacy Congratulates Senate On Passage ...
The Academy of Managed Care Pharmacy congratulates the Senate on passage of the Food and Drug Administration Revitalization Act (S. 1082). ...
Understanding The Threat To Dietary Supplements Part 2
Senators were taken off guard by the public outrage over the passing of bill S.1082 with language that can be used to seriously harass dietary supplements ...
Editorials Address User Fee Reauthorization Bill
Several newspapers recently published editorials on a bill (S 1082) approved last week by the Senate that would reauthorize the Prescription Drug User Fee ...
House Panel Considers Reauthorization of Medical Device User Fees
... timely fashion," but added that "that's not one of the must dos." The Senate passed a PDUFA reauthorization bill (S 1082) on May 9 ( CQ HealthBeat , 5/16).
Senators Defending the Big Pharma
... has revealed the apparent financial conflict of interest by US Senators who voted against the infamous S.1082 reimportation amendment. ...
Legalized Bribery Tracker at the Click of the Mouse, Coming Soon
So, for example, let’s say that you wanted to check on your Senator and how he or she voted on a bill (S. 1082) that passed the Senate last week (by a vote ...
US Senators financially enslave Americans as Indentured Servants ...
... has revealed the apparent financial conflict of interest by US Senators who voted against the infamous S.1082 reimportation amendment. ...
Understanding The Threat To Dietary Supplements Part 1
This is the exact same point the FDA is trying to get put into law through Senate bill S.1082 and HR.1561, which consumers have flooded the Senate on over ...

U.S. Congress - News Articles for S.1082 Medical Device User Fee Amendments of 2007



