Annual review and product listing update of registration

Blood Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices

OMB: 0910-0052

IC ID: 200688

Documents and Forms
Document Name
Document Type
Other-eSystem screen shots
Information Collection (IC) Details

View Information Collection (IC)

Annual review and product listing update of registration CBER
 
No Modified
 
Mandatory
 
21 CFR 607 21 CFR 607.21, 607.22, 607.25, 607.26 21 CFR 607.30, 607.31, 607.35 21 CFR 607.37, 607.39 21 CFR 607.40 21 CFR 607.65

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability
Other-eSystem screen shots 0052 Screen Shots - eBER.pdf Yes Yes Fillable Fileable

Health Consumer Health and Safety

 

2,812 0
   
Private Sector Businesses or other for-profits
 
   100 %

  Approved Program Change Due to New Statute Program Change Due to Agency Discretion Change Due to Adjustment in Agency Estimate Change Due to Potential Violation of the PRA Previously Approved
Annual Number of Responses for this IC 2,812 0 0 197 0 2,615
Annual IC Time Burden (Hours) 1,356 0 0 48 0 1,308
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

Title Document Date Uploaded
No associated records found
            Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.

© 2024 OMB.report | Privacy Policy