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PHARMACEUTICAL APPROVALS

Pharmaceuticals approvals are the last step in a long process of government testing. This topic tracks the approval of prescription and over-the-counter pharmaceuticals.

Pharmaceutical Approvals is part of Business Exchange, suggested by Evan Rappaport. This topic contains 1,743 news and 329 blog items. Read updated news, blogs, and resources about Pharmaceutical Approvals. Find user-submitted articles and reactions on Pharmaceutical Approvals from like-minded professionals.

News

Recent news on this topic.

UPDATE 1-Ipsen eyes U.S. Dysport launch clearance in mid-2009more

* FDA issues complete response letter to Ipsen for Dysport Biologics License Application * Says no additional clinical...

Coke scolded over labeling of Diet Coke Plusmore

The Food and Drug Administration has warned The Coca-Cola Co. that one of its products has a misleading nutritional...

FDA asks for more information on AstraZeneca's Seroquel XRmore

Discuss Financials Sponsored by:, , ) said Wednesday that it has received a complete response letter from the U.S.

U.S. OKs Novartis Gleevac to reduce recurring cancermore

patients with a rare type of stomach cancer, Novartis said on Friday. Gleevac is already approved by the Food and Drug...

Solvay Welcomes FDA Approval For Cholesterol Drugmore

-(Dow Jones)- Belgian chemical and pharmaceutical company Solvay SA ( SOLB.BT) Tuesday welcomed the U.S.

Colonoscopy prep pills carry kidney riskmore

is as clean as a whistle so your doctor can get an unobstructed interior view. ON THE WEB:FDA alert, consumer info In...

FDA questions Lilly, Amgen cancer drug trialsmore

U.S. health regulators are questioning whether clinical trials proposed by ImClone Systems and Amgen Inc will be...

FDA warns about drugs used before colonoscopymore

sternest safety warnings available to drugs used before colonoscopies, following reports of kidney damage in several...

Early Onset Approved for ADHD Drugmore

WEDNESDAY, Nov. 12 (HealthDay News) -- The U.S. Food and Drug Administration has approved a 30-minute onset of action...

The Pill Phone Medication Reminder Now Available Nationwide From Three...more

to identify specific pills. The software is the only interactive, wireless medication reminder application with...

ImmunoGen, Inc. Appoints James J. O'Leary, MD, as Vice President and C...more

as well as for the US. We're particularly pleased that Jim's background includes experience at the FDA as well as at...

Cholesterol-Fighting Drugs Show Wider Benefitmore

advocates who say it is more likely to lead to muscle deterioration and kidney problems. In 2005, the Food and Drug...

Roche Is Still Hunting Genentechmore

its $43.7 billion offer to buy out the rest of Genentech it does not already own, its pharmaceuticals chief said in an...

Obama expected to bolster FDA oversight of importsmore

WASHINGTON -- The Food and Drug Administration, bedeviled by a salmonella outbreak and tainted medicine from China, is...

Supreme Court Hears Case Involving Drug Labelsmore

November 3, 2008 ยท The Supreme Court hears arguments Monday in a case involving drug labels and the Food and Drug...

FDA approves new drug to treat overactive bladdermore

The U.S. Food and Drug Administration has approved a new drug, Toviaz (fesoterodine fumarate), to help patients...

Lilly CEO: FDA's Prasugrel Review Is 'Very Far Along'more

Our site map lists all the sections and tools of CNNMoney.com

Interview With Fund Manager Ed Owensmore

the government offering universal coverage without their help. SM: And you like smaller biotech firms too? EO: Vertex...

Mylan gets tentative FDA OK on prostate drugmore

PITTSBURGH - Mylan Inc. said Wednesday it received tentative approval from the Food and Drug Administration for a...

Abbott: FDA Needs More Time To Review TriLipixmore

Continuing a string of drug-approval delays, the U.S. Food and Drug Administration has told Abbott Laboratories (ABT)...

U.S. officials ask bottle makers to avoid using bisphenol Amore

use the chemical bisphenol A in their manufacturing because, they said, it was potentially harmful to infants.

US clears Lev Pharma drug for rare swelling diseasemore

WASHINGTON, Oct 10 (Reuters) - U.S. health regulators on Friday approved Lev Pharmaceuticals Inc's (LEVP.

FDA to Continue Review of Alogliptin NDAmore

that Takeda Global Research and Development Center, Inc., a wholly owned U.S. subsidiary, received notification that...

R.J. Reynolds' New Smokeless Products Will Appeal to Children and Show...more

quitting, and their introduction underscores the urgent need for Congress to pass pending legislation that grants the U.

FDA: No Quick Decision on Kids Cold Medsmore

of an immediate ban on cough and cold medicines for young children, saying it might cause unintended harm.

Top Sources: Pharmaceutical Approvals

  • myharvardnews.com
  • pharma-iq.com
  • bloomberg.com
  • Forbes.com
  • pennystockdd.com
  • MarketWatch
  • chicagotribune.com
  • US News
  • Financial Times
  • Reuters

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Associate Director, Drug Regulatory Affairs Product Group Boehringer Ingelheim | Connecticut
Posted: May 19
Pharmaceutical Sales Specialist - CV SPEC4 AstraZeneca | Charlottesville, VA
Posted: Jun 19
Executive Pharmaceutical Sales Specialist (Manhattan North, NY) Shire Pharmaceuticals | Chesterbrook, PA
Posted: May 17
Pharmacist (Investigational Drug Research Quality Program Manager) United States Department of Veterans Affairs | Martinez, CA
Posted: Jun 13
Drug Safety Physician Baxter International | Deerfield, IL
Posted: Apr 26

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