Agency Information Collection Activities; Announcement of OMB Approval; Postmarketing Adverse Drug Experience Reporting.   (23OCT02)
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Agency Information Collection Activities; Submission for OMB Review; Comment Request; Postmarketing Adverse Drug Experience Reporting.    (22JUL02)
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Postmarket Surveillance.    (06JUN02)
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Agency Information Collection Activities; Proposed Collection; Comment Request; Postmarketing Adverse Drug Experience Reporting.    (25FEB02)
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