Compliance Program Guidance Manual Chapter – 42 Blood and Blood Products Inspection of Licensed In-Vitro Diagnostic (IVD) Devices 7342.008
Titel:
Compliance Program Guidance Manual
Chapter – 42 Blood and Blood Products
Inspection of Licensed In-Vitro Diagnostic (IVD) Devices
7342.008
Internet:
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/
Dokumentenart:
Guidance Manual
Inhalt:
Compliance Program CBER Biologics