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image: Congress Passes “Right to Try” Bill

Congress Passes “Right to Try” Bill

By Jim Daley | May 23, 2018

Medical groups have criticized the legislation, which will give terminal patients access to experimental treatments, as dangerous and unnecessary.

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image: FDA Approves Drug to Ease Symptoms of Opioid Withdrawal

FDA Approves Drug to Ease Symptoms of Opioid Withdrawal

By Catherine Offord | May 17, 2018

Lucemyra is the first non-opioid drug to be approved in the U.S. specifically for this purpose.

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Two patients became legally blind after receiving treatments at the facilities.

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The Scientist looks at one such Houston-based purveyor that has been treating patients abroad for years with mesenchymal stem cells.    

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Rather, the breast cancer mutation screen was classified as a type of medical device with obligations for the company to reduce risks to customers.

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image: Recipients of Experimental Herpes Vaccine File Lawsuit

Recipients of Experimental Herpes Vaccine File Lawsuit

By Catherine Offord | March 15, 2018

The suit claims that Rational Vaccines, the company of recently deceased researcher William Halford, violated US and international laws when it carried out the procedure.

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The agency gave personal genomics company 23andMe the green light to screen samples for breast cancer–related genetic mutations.

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image: FDA Report on BPA’s Health Effects Raises Concerns

FDA Report on BPA’s Health Effects Raises Concerns

By Ashley Yeager | February 28, 2018

The pre-peer review assessment finds the compound has “minimal effects,” but endocrinologists and others say key data have yet to come out.

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image: CDC, FDA Warn Against Kratom Use

CDC, FDA Warn Against Kratom Use

By Jim Daley | February 26, 2018

The herbal supplement, deemed an opioid by the FDA, was recently linked to a Salmonella outbreak in 20 states. 

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image: New Automated Tool Monitors Clinical Trial Reporting

New Automated Tool Monitors Clinical Trial Reporting

By Diana Kwon | February 22, 2018

The watchdog website FDAAA TrialsTracker names and shames human studies that breach the FDA’s requirements for reporting results.

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