More than 120 HCT/P providers from across the U.S. choose Memorial Blood Centers for quality testing services. In close partnership with reproductive medicine providers, cryobanks, university stem cell programs and biotech firms, we deliver:
- A comprehensive menu of FDA-approved tests, including male and female test panels for reproductive medicine providers and cryobanks
- Rapid and accurate results to meet the critical timing needs of our customers
Regulated and licensed by the FDA to conduct HCT/P testing, Memorial Blood Centers uses only FDA-approved test kits to test donors of human cells, tissues, and cellular and tissue-based products.
Requirements for West Nile Virus Testing
The FDA has issued a guidance for industry that describes the FDA’s approach to reducing the risk of transmission of West Nile Virus (WNV) from living donors of HCT/Ps. The FDA is recommending the use of an FDA-licensed NAT to test living donors on HCT/Ps recovered from June 1st through October 31st every year. For establishments intending to import HCT/Ps into the United States, the FDA recommends that donors be tested year-round for WNV by NAT.
A copy of the guidance can be downloaded here. Memorial Blood Centers’ donor testing menu includes an FDA-cleared WNV test.
HCT/P screening tests
|HBsAG||HIV Ag/Ab Combo|
|Anti-HTLV I/II||Syphilis Screen|
|Antibody to CMV (Total)||NAT Multiplex (HIV/HCV/HBV) PCR|
|West Nile Virus NAT||Chlamydia trachomatis PCR|
|Zika Virus PCR||Neisseriagonorrhoeae PCR|
Confirmatory/supplemental testing is also available on select screening tests listed above, including:
|Geenius HIV ½||HCV Ortho|
|HTLV Blot 2.4||HBsAg Neutralization|
|Abbott Chagas ESA||Antibody to CMV IgM ELISA|
|Antibody to CMV IgG ELISA|
Learn more about Reproductive & IVF Donor Testing.