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Subjects (1-5 of 5)
Collection And Preservation Blood Government Policy United States
1
Guidance for FDA reviewers premarket notification submissions for blood and plasma warmers.
Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, [2001] 2001
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Axe Federal Documents Online
HE 20.4802:P 91/5
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Available
2
Guidance for FDA reviewers premarket notification submissions for empty containers for the collectio
Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, [2001] 2001
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Axe Federal Documents Online
HE 20.4802:P 91/7
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3
Guidance for industries variances for blood collection from individuals with hereditary hemochromato
Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, [2001] 2001
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Axe Federal Documents Online
HE 20.4802:B 62/2
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4
Guidance for industry notifying FDA of fatalities related to blood collection or transfusion.
Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, [2003] 2003
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Axe Federal Documents Online
HE 20.4802:F 26
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5
Guidance for industry recommendations for collecting red blood cells by automated apheresis methods.
Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, [2001] 2001
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Axe Federal Documents Online
HE 20.4802:C 67
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