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Regenerative Medicine

Stem Cell Therapy


Practice Alliance, Inc is NOT liable for the intended use of any of its products. Practice Alliance, Inc does not intend to define, suggest, alter or approve of any kind of “practice of medicine” performed by the administering physician(s) instead relying on the IND and/or Clinical Trial IRB to determine safe practices of use of the Cord Blood Stem Cell Product(s)(CBSC), Amniotic Fluid, Amniotic Tissue, Human Umbilical Cord Blood Plasma (hUCBP), Wharton’s Jelly, and Wharton’s Jelly (MSC). These products are for Research Use Only.

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Stem cells are collected and distributed by a cGMP laboratory in Orange County, CA with their products tested through third party CLIA certified labs. Umbilical cord stem cells are derived from young day zero cells with minimal manipulation for cell preservation. All birth tissues are received from normal full-term pregnancies within the US at full consent of the donor. Donor is pre-screened through medical record review and evaluation of prenatal tests. The donated blood/tissue is tested for a panel of infectious disease; testing identified in the certificate analysis that comes with each product. Practice Alliance, Inc. is a distributor and assumes no liability or responsibility for the effects of therapy. The information collected by Practice Alliance, Inc. is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition.

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