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Pfizer Documents (PHMPT/FDA)

Pfizer Bla Submission

Pfizer 16 Plus Documents

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Pfizer Global Regulatory Affairs
Pfizer Inc .
400 Arcola Road Collegeville, PA 19426
Global Product Developm ent
11August 2021
Marion Gruber, Ph.D.
Director
Office of Vaccines Research and Review 
Food and Drug Administration
Center for Bi ologics Evaluation and Research
Document Control Center
10903 New Hampshire Avenue
WO71, G112
Silver Spring, MD 20993 -0002THIS DOCUMENT CONTAINS CONFIDENTIAL 
AND/OR TRADE S ECRET INFORMATION 
THAT IS DISCLOSED ONLY IN CONNECTION 
WITH THE LICENSING AND/OR 
REGISTRATION OF PRODUCTS FOR PFIZER 
INC OR ITS AFFILIATED COMPANIES.  THIS 
DOCUMENT SHOULD NOT BE DISCLOSED OR 
USED, IN WHOLE OR IN PART, FOR ANY 
OTHER PURPOSE WITHOUT THE PRI OR 
WRITTEN CONSENT OF PFIZER INC.
Re: BLA 125742
COVID -19 mRNA Vaccine ( BNT162/PF -07302048 )
Response to FDA ’s04 August 2021 Information Request Regarding the Lot 
Release Protocol Template
Dear Dr. Gruber,
Reference is made to the Biologics License Application (BLA) submitted 18 May 2021 for 
the COVID -19 mRNA Vaccine (BNT162/PF -07302048) developed b y BioNTech and Pfizer
under BB -IND 19736 for the prevention of COVID -19caused b y SARS -CoV -2in 
individuals ≥16 y ears of age.
On 04August 2021, the Agency  sentan Information Request regarding the lot release 
protocol template . The requested information is provided in Response to 04 Aug 2021 FDA 
Information R equest –Lot Release Protocol (LRP) Template in Module 1.11.1.
A number of questions ar e included in this response. Pfizer/BioNTech respectfully  request 
feedback not later than 18 August 2021.
Should y ou have any  questions regarding this submission, or require additional information, 
please contact me via phone at 215 -280-5503; via facsimile at 845-474- 3500; or via e -mail at 
[email protected] .
FDA-CBER-2021-5683-1149526
Marion Gruber, Ph.D., Director Page 2of 2
BLA 125742 11August 2021
Pfizer Confidential
Page 2Sincerel y,
Elisa Harkins
Global Regulatory  Lead
Global Regulatory Affairs – Vaccines
CC: Ramachandra S. Naik, Ph.D.
CC: Michael Smith, Ph.D.
CC: Laura Gottschalk, Ph.D.
FDA-CBER-2021-5683-1149527