mCELL™

A cGMP-Manufactured Off-The-Shelf Bone-Marrow Stem Cell

mCELL™ is a donor sourced bone marrow-derived mesenchymal stromal cell product manufactured in an FDA-registered, cGMP facility, cryopreserved for off-the-shelf clinical use, and supplied exclusively to licensed physicians for localized use.

Product Specifications

Cell Type

Bone marrow-derived mesenchymal stromal cells

Cells per Vial

30 million viable living cells

Donor Age

18 to 25 years

Formulation

Cryopreserved, ready for thaw and immediate use

Shipping

Product ships in a qualified dry ice package.

Documentation

Full Certificate of Analysis

Why 30 Million Cells

Meta-analyses of randomized controlled trials evaluating intra-articular MSC therapy consistently identify doses at or below 25 to 30 million cells as the tier associated with statistically significant functional improvement at 12 months. Increasing the dose beyond that threshold has not shown additional benefit. Excess cell concentration can reduce viability in the joint environment, where cells compete for limited space and nutrients. mCELL™ is calibrated at this clinically supported threshold.

Certificate of Analysis

mCELL™ comes with a lot-specific Certificate of Analysis (COA). A COA is a document that summarizes the testing and quality verification performed on a product before it is released for clinical use. It provides physicians with transparent, objective data about what is in a given lot and confirmation that it meets predefined quality and safety specifications.

For biologic products, a COA typically includes:

  • Lot identification and traceability: unique lot number, manufacturing site, and key dates
  • Identity testing: confirmation of the intended cell type
  • Purity and quality attributes: including absence of contaminants
  • Viability: confirmation that cells are alive and functional at the time of release (and, where applicable, post-thaw)
  • Sterility and safety testing: results for microbial contamination and other release criteria
  • Release specifications: the defined criteria each lot must meet to be approved for distribution

A COA is part of a broader quality system designed to ensure consistency, traceability, and compliance with applicable regulatory standards. It allows physicians to make informed decisions with confidence, based on clearly documented product characteristics for each lot.

Shipping and Handling

mCELL™ is cryopreserved and shipped in a qualified dry ice package designed to maintain viability, cell count, and sterility during transport. TAVRA provides thawing instructions to the clinical site in advance of injection. 

No on-site cell processing, manipulation, or centrifugation is required.

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