The standard
for regenerative
medicine.
The catalog, organized the way clinicians think.
Five stages, one chain of custody.
Sourcing
Donor screening, raw-material qualification, certificate-of-origin on every input. CellGenic operates under appropriate regulatory frameworks with full compliance.
Lab
ISO Class 7 cleanroom. Cell expansion, vesicle isolation, peptide synthesis under one roof.
QC / Compliance
Sterility, endotoxin, mycoplasma, identity, potency. Every batch. COA shipped with product.
Packaging
Lyophilized or cryo-preserved as the protocol requires. Tamper-evident, batch-stamped.
Shipping
Validated cold-chain to four countries. Temperature logger in every box. Signature on receipt.
What a laboratory looks like when no detail is delegated.
Produced at Cellgenic Labs — Florida, USA.
cGMP-certified facility. ISO 7 cleanroom. ISO 20387 biobanking. The same lab characterizes the cells, fills the vials, signs the COA, and ships the cooler — nothing white-labeled in.
Every batch, fully characterized.
Sterility, endotoxin, mycoplasma, identity, potency. The COA ships in the box and lives in your provider portal forever.
A clinical advisory board, not a marketing one.
Our protocols are reviewed by practicing physicians in the four countries we serve. Their notes are how the catalog evolves.
CellGenic is a provider platform.
The standard for regenerative medicine.