Sunday November 22 2009 | Biotechnology feed | All feeds
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Robert F. Munzner, Ph.D.
Download detailed PDF Members: If you are a medical device importer, manufacturer or inventor, I can answer your questions concerning the FDA requirements for introducing a new device into commerce. If you are physician planning to test a new medical device using human subjects, I can explain the rules for an investigational device exemption. If you want someone to prepare the necessay paperwork for you, I am affiliated with a full-service organization that can do the job for you. I specialize in the evaluation of the devices used in neurosurgery, neurology, and psychiatry.I have more than twenty years' experience in device evaluation. My doctorate is in biomedical engineering from the University of Virginia, and I am post doctoral fellow of the Johns Hopkins University School of Medicine.
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