FDA Guidance for Industry How to Complete the Vaccine Adverse Event Reporting System Form (VAERS-1)

Titel:
FDA Guidance for Industry How to Complete the Vaccine Adverse Event Reporting System Form (VAERS-1)
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/Vaccines/UCM164319.pdf

Dokumentenart:
Guidance for Industry
Inhalt:
Informationen zum Formblatt zur Meldung von Nebenwirkungen

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