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Vaccines, Blood & Biologics
From: Pracht, Leigh
Sent: Wednesday, January 16, 2013 8:14 AM
To: Pracht, Leigh
Subject: FW: Information Request BLA 125466/0
Our Reference: BL 125466/0
Novo Nordisk Inc.
Attention: Cindy Cao, PhD
January 16, 2013
Sent by email
Dear Dr. Cao:
We are reviewing your October 15, 2012 biologics license application (BLA) for Antihemophilic Factor (Recombinant), Plasma/Albumin Free [NovoEight]. We determined that the following information is necessary to continue our review:
1. For the DS please provide the complete validation / qualification reports for the -----------------------------(b)(4)-------------------------- tests.
2. For the DP please provide the complete validation / qualification reports for the Bacterial Endotoxin and Sterility tests.
The review of this submission is on-going and issues may be added, expanded upon, or modified as we continue to review this submission.
Please submit your response to this information request as an amendment to this file by March 15, 2013 referencing the date of this request. If you anticipate you will not be able to respond by this date, please contact the Agency immediately so a new response date can be identified.
The action due date for this file is October 15, 2013.
If you have any questions, please contact me at (301) 827-6116.
Leigh A. Pracht
Regulatory Project Manager
WOC1; RM562N; HFM-380
1401 Rockville Pike
Rockville, MD 20852
Fax: 301- 827-2857
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