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Accreditations and Registrations |
Registered with the Food and Drug Administration
(FDA)
The Food and Drug Administration (FDA) has
already taken initial steps to regulate the
field of cord blood banking. We welcome the
regulation because being inspected by the FDA
provides us with the good housekeeping seal of
approval. It gives you the quality assurance you
need in order to know that you have chosen a
credible organization with which to store your
child's cord blood. We are proud to be among the
first cord blood banks to have registered with
the FDA.
Licensed with PharmaStem under U.S. Patents
5,004,681, 5,192,553, 6,461,645, 6,569,427 and
6,605,275

NECBB is among the first cord blood banks to
enter into a licensing agreement with
PharmaStem Therapeutics, Inc., the holder of
five U.S. patents related to processing
umbilical cord blood used by most cord blood
banks. The license ensures that your baby's
cells are legally protected. Cord blood banks
without a PharmaStem license risk being found
guilty of patent infringement, jeopardizing the
safety of the cells they are storing. Our
PharmaStem license also protects doctors,
midwives and hospitals as well from the threat
of legal penalties.
Our
laboratory has a federal CLIA
CMS regulates all laboratory testing performed
on humans in the U.S. through the Clinical
Laboratory Improvement Amendments (CLIA). The
objective of the CLIA (Lic. #: 22D0725005)
program is to ensure quality laboratory testing.
Licensed by the States of New York , California
and Massachusetts
Our state of the art laboratory is fully
compliant with both Federal and State clinical
laboratory regulations for processing your
child's cord blood. The States of Massachusetts
(Lic. # 2337), California (Lic. # CNC_80400) and
New York (Lic. # SC112) have issued regulations
regarding the cord blood banking, and we are
licensed by all three states.