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    Occasionally FDA approves a medical device before all long-term questions about its safety and effectiveness have been answered. If these questions can only be answered by a large clinical study, FDA may approve the device for sale but require the manufacturer to continue to study its safety and effectiveness. Such a study is called a "post approval study." This page lists the post approval studies begun after January 1, 2005, and their progress. , USA
 
    Germany
 
    Swiss Federation dedicated to the Medical Device Industry, Switzerland
 
    Finland
 
    USA
 
    Dedicated to improving the lives of people with orthopedic disabilities by providing: -Consumer awareness programs regarding enhanced material research for hip and knee implant surgery. -Supporting the orthopedic medical community by funding educational symposia. -Providing early stage development funds for enhanced material research for implant surgery., Australia
 
    The Fraunhofer Institute for Cell Therapy and Immunology IZI investigates and develops solutions to specific problems at the interfaces of medicine, life sciences and engineering. The Institute develops, optimizes and validates methods and products for the Business Units Drugs, Cell Therapy, Diagnostics and Biobanks., Germany
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