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NewsFDA Responses to HRSA    February 22, 2012

FDA Responses to HRSA

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The FDA has responded to questions regarding cord blood licensure that were posed by HRSA at a meeting held in July.  These questions were compiled from those asked by representatives of cord blood banks at the NCBI All Bank Meeting held in DC at the end of March.  We hope you find the responses, which we’ve been cleared to share, helpful.

 FDA Responses to HRSA PDF Document

Working Groups Directory
 
WORKING GROUPS LEADER
Consent Issues (Mom) Kathleen Sazama
Sterility John McMannis
Vendor Qualification Sue Armitage
Potency and Release Joanne Kurtzberg
Thaw and Administration Kathy Welte
Transportation and Shipping Fran Rabe
Post BMT Doug Rizzo
Adverse Event Investigation John Miller
Labeling Becky Haley
Expiration Dates/Stability Kathy Fortune
Validation Templates Mary Beth Fisk

 

 
 

 

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