U.S. generic drug rules have been manipulated by brand-name drug companies to keep cheaper competition off the market, a report says.
Gordon Gund, Gund Investment Corp. chairman & CEO, who lost his sight 40 years ago, discusses the promising work being done to find a cure for blindness.
Gordon Gund, Gund Investment Corp. chairman & CEO, who lost his sight 40 years ago, discusses his goal to raise $100 million to fund research for a cure for blindness.
Larry Jasinski, ReWalk Robotics CEO, discusses how the FDA's decision will likely improve the lives of wheelchair bound people. This is such groundbreaking technology that the FDA put a new classification code for this product, explains Jasinski.
The U.S. Food and Drug Administration warned that popular acne products can cause rare but serious and life-threatening allergic reactions.
Michael Bonney, Cubist Pharmaceuticals CEO, discusses the FDA's approval of Sivextro, a new antibiotic designed to treat skin infections. Bonney also explains why so many pharma companies have left the antibiotic space.
Genetics startup 23andMe said it is one step closer to resuming sales of its full-fledged health product.
POM Wonderful may take Coke to court to accuse it of misleadingly marketing one of its Minute Maid juices, the U.S. Supreme Court said.
Ariad Pharmaceuticals CEO Dr. Harvey Berger, says investors are responding to his company's better overall picture, and the progress on its leukemia drug Iclusig.
Two companies issued voluntary recalls of hummus dips and walnuts sold at major retailers after listeria was detected in samplings of the products.
Unlike prescription drugs the FDA does not inspect vitamins before they hit the market. Neil Thanedar, LabDoor CEO, provides independent product safety research and grading to help consumers learn what's really inside their vitamins.
Lawmakers in four states are considering changing the rules to allow terminally ill people access to experimental drugs before they have FDA approval. Kenneth Goodman, University of Miami, thinks this would be a bad bet for patients. Miles Nadal, MDC Partners Chairman & CEO, weighs in.
The FDA said that people should use daily aspirin therapy only after assessing the benefits and risks.
CNBC's Seema Mody, Bob Pisani and Tyler Mathisen looks at today's "Power Lunch" stories, including news the FDA is proposing the first regulations on electronic cigarettes.
Blu eCigs founder Jason Healy, discusses the FDA's "science based" proposed rules that call for strict regulation of electronic cigarettes. The measures will range from age restrictions to health warnings.
The FDA is considering new rules for e-cigarettes that are similar to those that currently govern tobacco products, reports NBC's Tom Costello.
Sarepta Therapeutics CEO Chris Garabedian discusses the prospects for what he calls a "potential accelerated approval" for its Duchenne muscular dystrophy drug Eteplirsen.
Sarepta Therapeutics is developing a drug for Duchenne muscular dystrophy. Its CEO Chris Garabedian discusses challenges the drug Eteplirsen has faced before the FDA.
With rising food rates and an increase in food imports, food fraud is a growing problem that costs the industry up to $15 billion a year.
The Cefaly device uses a mild electric current to prevent migraines.