FDA Guidance for FDA Reviewers Premarket Notification Submissions for Blood and Plasma Warmers

Titel:
FDA Guidance for FDA Reviewers Premarket Notification Submissions for Blood and Plasma Warmers
Herkunft/Verlag:

Freedom of Information Staff, (HFI 35), Food and Drug Administration, Rm. 12 A - 30, 5600 Fishers Lane, Rockville, MD 20857, USA, http://www.fda.gov/ , http://www.fda.gov/downloads/BiologicsBloodVaccines/GuidanceComplianceRegulatoryInformation/Guidances/Blood/ucm062955.pdf

Dokumentenart:
Guidance for FDA Reviewers
Inhalt:
Überblick über die erwarteten Informationen eines FDA Gutachters bei der Premarketed Notification vom Blut oder Plasma Warmers

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