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  • How can postmarket medical product safety data collection be integrated into workflow of clinical practice at point-of-care while avoiding imposition of undue burdens on HCPs, patients, and health care institutions?

  • How readily can existing systems be used or be modified to serve as dynamic surveillance loops

    • (e.

      g., constant integration of data collection from,

analysis, and feedback of information to health care practitioners and patients at the point-of- care)?

©sagcs 2007

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