CNBC's Meg Tirrell looks at the screening protocols the U.S. is considering to stop Ebola from entering the country.
CNBC's Meg Tirrell, and Dr. Moncef Slaoui, GlaxoSmithKline, discuss the latest efforts to develop an Ebola vaccine.
CNBC's Meg Tirrell reports the FDA has given permission for drugmaker Chimerix to provide an antiviral drug to Thomas Eric Duncan, as President Obama looks at ways to strengthen passenger screening for Ebola.
Kevin Conroy, Exact Sciences chairman & CEO, provides details on a potential major breakthrough in the fight against colon cancer.
The FDA approved the first screening test for colon cancer that uses patients' DNA to help spot potentially deadly tumors and growths.
Indiana Attorney General Greg Zoeller, has joined the fight to urge the FDA to strengthen electronic cigarette regulations and adopt new policies to protect minors from harmful flavoring and addictive electronic cigarettes.
Scott Gottlieb, M.D., American Enterprise Institute, explains why he thinks excessive FDA regulations are stalling innovation in medical technology.
Scott Gottlieb, M.D., American Enterprise Institute, and Jeff Allen, Friends of Cancer Research executive director, discuss the FDA's drug approval process and the need in some cases to allow access to experimental therapies.
Terminally ill patients are increasingly seeking access experimental drugs outside clinical trials, but drug companies often decline these requests. A look at why.
A dose of experimental serum arrived in Liberia to be tried on a U.S. charity worker—but there was only enough for one of the two infected workers, NBC.
The way consumers would be informed when their food has been genetically engineered is being battled in Congress and among advocacy groups.
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.