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Friday, September 8, 2017 at 03:51 PM
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Just as cannabis is gaining traction as a legitimate treatment option for military veterans, the U.S. Food and Drug Administration has given the "breakthrough therapy"... [Read More]
* Granted U.S Food And Drug Administration 510(K), class II approval to market & sell its Prizma Medical Smartphone Jacket in U.S. Source text for... [Read More]
A teacher here was recently selected as one of only 30 teachers nationwide to complete an elite food science training program.Apple Valley High School teacher... [Read More]
The Food and Drug Administration on Wednesday approved the first-ever gene therapy in the US. The drug, called Kymriah, is a highly personalized cancer... [Read More]
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The US Food and Drug Administration (FDA) has just issued an advisory note recalling 465,000 radio-controlled implantable cardiac pacemakers because of fea... [Read More]
AMAG Pharmaceuticals announces broadening of labelAMAG Pharmaceuticals, of Waltham, announced that the U.S. Food and Drug Administration accepted its submission to broaden the existing label... [Read More]
The US Food and Drug Administration (FDA) has approved Kymriah (tisagenlecleucel) for certain children, adolescents, and young adults with a form of acute lymphoblastic leukemia... [Read More]
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The US Food and Drug Administration (FDA) has announced a recall of 465,000 pacemakers after the devices were found to be vulnerable to hacking. [Read More]
The US Food and Drug Administration (FDA) recently recalled approximately 465,000 pacemakers made by the company Abbott's (formerly St. Jude Medical) that were vulnerable to... [Read More]
In striking contrasts, a university-based team just announced it has developed a five-dollar treatment that completely abolishes cancer in the same week news headlines hailed... [Read More]
When the Food and Drug Administration (FDA) gave approval to a new leukemia therapy this week it marked the end of research and clinical trials... [Read More]
The Food and Drug Administration is alerting people to a voluntary recall of 465,000 pacemakers after security vulnerabilities were discovered that could let hackers reprogram... [Read More]
This week, the Food and Drug Administration approved a new treatment for Leukemia.  ... [Read More]
The U.S. Food and Drug Administration on Friday approved an altered dose of the drug Mylotarg to treat a distinctive type of acute... [Read More]
A new drug was approved by the Federal Drug Administration and will be used soon to treat MS. [Read More]
The U.S. Food and Drug Administration (FDA) on Friday approved Pfizer Inc's drug, Mylotarg, for certain patients with acute myeloid leukemia (AML), re-clearing a drug... [Read More]
The U.S. Food and Drug Administration (FDA) on Friday approved Pfizer Inc's drug, Mylotarg, for certain patients with acute myeloid leukemia (AML). [Read More]
The Food and Drug Administration is recalling 465,000 pacemakers to be uploaded with new secure software after discovering cyber-security vulnerabilities in its system which would... [Read More]
The US Food and Drug Administration classifies MDMA—the primary active chemical in ecstasy and molly—as a Schedule 1 drug. From the perspective of the US…... [Read More]
The U.S. Food and Drug Administration has approved a novel cancer treatment that resulted in 83% of patients with resistant leukemia going into remiss... [Read More]
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