News

Search:

Former FDA Commissioner: 'New Paradigm Shift' Means Agency Must Approve Treatments Faster

0 Likes

Former US Food and Drug Administration (FDA) Commissioner Mark McClellan, now a member of the think tank The Brookings Institute, penned an opinion piece in The Hill in which he argues FDA must take Read More...

Tags:

Bennet

Bill

Breakthrough Product Designation

Brookings

Burr

Congress

Friends of Cancer Research

Hatch

Legislation

McClellan

Senate

Sigal

Legislation to Make FDA's Regulatory Calculus More Transparent Introduced in Congress

0 Likes

Sens. Richard Burr (R-NC) and Tom Coburn (R-OK) introduced legislation that would reform the US Food and Drug Administration’s (FDA) regulatory transparency by mandating the agency submit to Congress Read More...

Tags:

Act

Bill

Burr

Coburn

Congress

FDA

Legislation

PATIENTS FDA Act

Regulatory

Senate

Transparency

Senators Draft Bill to Expedite Drug Approval

0 Likes

A piece of legislation introduced this week by a bipartisan group of three Senators would “expedite US Food and Drug Administration (FDA) approval and provide more flexibility when a drug or treatment Read More...

Tags:

ABTP

Act

Approval

Bennet

Burr

Clinical Trials

Committee

Congress

drug

FDA

Hatch

HELP

Innovation

Senate

RF Today is Regulatory Focus' daily news brief. Each edition contains the top global regulatory news stories about pharmaceuticals, medical devices, biotechnology and more. Learn more

Most Viewed
Most Popular

Most Viewed

China's SFDA Becomes CFDA amidst Consolidation of Power and New Leadership 25 March 2013
FDA Plans Huge Cardiovascular Registry With Focus on Medical Devices 2 April 2013
In Unprecedented Shift, EU Parliament Proposes Premarket Authorization for Medical Devices 15 April 2013
Goodbye, KFDA: Korean Regulator Gets New Name, Decentralized Authority After Reorganization 28 March 2013
FDA Gets Go-Ahead for Study of DTC Advertising and Social Media 18 April 2013
UPDATED: President's Budget Proposal Calls for Small Increases at FDA, but Big Changes for Industry 11 April 2013
IBM Awarded Huge Contract to Modernize Regulatory Review Processes at FDA 29 April 2013
New FDA Document Clarifies IND Process for Drugs, Biologics and Biosimilars 30 April 2013

New Regulatory Focus Apps for iPad and iPhone

Stay Connected:

Regulatory Focus is for regulatory professionals written by regulatory professionals.

The publication takes a look at the important topics facing regulatory professionals in a changing global healthcare landscape. From topics ranging from research and development to labeling and marketing, the articles try to analyze, inform, and educate readers about the issues at the forefront of the industry.

Rated as the number one benefit by the members of RAPS, Regulatory Focus strives to provide the best and most current information to regulatory professionals so they can succeed and advance at every stage in their careers.

For questions or comments on our content or to find out more about Regulatory Focus, please visit our About RF page.

News

Former FDA Commissioner: 'New Paradigm Shift' Means Agency Must Approve Treatments Faster

Legislation to Make FDA's Regulatory Calculus More Transparent Introduced in Congress

Senators Draft Bill to Expedite Drug Approval

Get RF Today