FDAMedical Technology

Q&A: Bioethicist Leigh Turner on the worrisome boom in unregulated stem cell clinics

(By Megan Molteni for STAT)

In 2016, the Food and Drug Administration put the emerging stem cell cottage industry on notice. At the time, a few hundred clinics were peddling experimental stem cell therapies costing between $2,000 and $25,000 for conditions ranging from chronic pain to autism to multiple sclerosis without solid scientific evidence that they worked. Federal regulators asserted that the stem cells being sold — usually taken from a patient’s body and slightly processed before being re-injected — were drugs, and therefore required a rigorous approval process.  Continue reading here…

 

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