Hi, I'm new to this list. I work for the Sunlight Foundation, and Micah Sifry suggested that folks here might be able to help me with some information I'm looking for. For an investigation on transparency of health information, I've been tracking an example of a particular medical device manufactered by a U.S. company. The company has marketed this device in Europe since 2005; however, it does not do so in the U.S. because it has not received approval by the Food and Drug Administration.
I'm wondering if there's some way to track how this device has been marketed in Europe, in particular whether there have been any reports of problems associated with it. It would also be helpful to know how widely it's marketed. In the U.S. the source of much of this information would be the FDA, but I don't know what the equivalent would be for the EU. Any advice or tips would be much appreciated. Thanks, Nancy Watzman -- Nancy Watzman consultant Sunlight Foundation 2349 Dexter Street Denver, CO 80207 303.329.8563 (voice) 303.514.0888 (cell)
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