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Home » FDA Calls Study Criticizing HDE Biased, Riddled With Omissions
FDA Calls Study Criticizing HDE Biased, Riddled With Omissions
February 11, 2011
The FDA has found several flaws in a study that claims its humanitarian device exemption (HDE) program is being improperly used to allow deep brain stimulation (DBS) to treat resistant obsessive-compulsive disorder (OCD).