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Federal Register / Vol. 64, No. 160 / Thursday, August 19, 1999 / Proposed Rules DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 600 Docket No. 98 N 0815 Plasma Derivatives
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What is plasma derivatives and oformr?
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Information such as product name, manufacturer, batch number, quantity distributed, and recipient details must be reported on plasma derivatives and oformr.
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