The Community Blood Center is committed to providing a reliable blood supply, and has a long history of outstanding regulatory compliance. Blood products are processed, tested, labeled, and manufactured in compliance with current Good Manufacturing Practices (cGMP) as defined in the Code of Federal Regulations (CFR). Click on one of these files to view our FDA, AABB, or CLIA certificates.

FDA Registration Appleton 2018
AABB Certificate of Accreditation
CLIA Certificate of Accreditation
Maryland Medical Laboratory Permit

Circular of Information

The Circular of Information for the Use of Human Blood and Blood Components was prepared jointly by AABB, the American Red Cross, America's Blood Centers, and the Armed Services Blood Program.


  • For products collected as of November 15, 2017:
    • Zika Virus Testing - A licensed nucleic acid test (NAT) for Zika Virus RNA has been performed and found to be nonreactive.

  • For products collected¬†November 10, 2016 - November 14, 2017:
    • Zika Virus Testing - Units labeled as negative for Zika virus RNA were tested individually (IDT) with an investigational nucleic acid test (NAT) and found to be nonreactive.