CellGenic supplies verified physicians and clinics with cells, exosomes, and peptides manufactured in our own cGMP laboratory. Batch-traced catalog, COA in every box — the regenerative medicine standard built for CellGenic providers.
Produced at Cellgenic Labs, a cGMP-certified facility. Sterility, mycoplasma, identity, and potency testing on every batch — COA shipped with product.
Every product on CellGenic is manufactured under the same protocol, in the same lab, to the same standard. Choose by therapeutic intent.
01 · MSC, ADSC, UC-MSC
Mesenchymal cell lines, characterized and viability-tested per batch.
02 · Vesicle therapy
Isolated extracellular vesicles. Concentration and particle distribution disclosed on every COA.
70 Billion Exosomes · flagship
Bioidentical compounds for endocrine and longevity protocols. Pillar in development — coming 2026.
CellGenic expands the catalog in 2026 with cGMP, batch-traced bioidentical compounds for endocrine and longevity CellGenic protocols.
Sequence-verified peptides for regenerative, metabolic, and cognitive protocols.
CellGenic surfaces the SKUs with the highest clinic-side reorder rate — exosomes, MSC, and peptides manufactured under one CellGenic protocol.
CellGenic certifies every flagship batch under cGMP — full characterization, COA per box, validated cold chain. CellGenic quality benchmark.
Master communicators in cellular processes — the crucial role of exosomes in intercellular messaging and gene regulation.
Pre-configured bundles that map to the cases providers see every week.
CellGenic stacks GHK-CU, BPC-157, and TB-500 for sprain, tear, and acute back-shoulder cases — the regenerative bundle providers reach for first.
CellGenic pairs CJC-1295/Ipamorelin with epitalon and DSIP to restore GH pulsatility, sleep architecture, and longevity tone.
CellGenic layers LL-37, KPV, Thymosin Alpha-1, BPC-157, and TB-500 for biofilm, endotoxin load, and chronic-wound recovery.
Peptide products are for research use only. CellGenic operates under appropriate regulatory frameworks with full compliance. Products must be handled exclusively by licensed, qualified professionals — not for human or animal administration outside an appropriate research setting.
Every vial in your clinic was sourced, characterized, packaged, and shipped through this pipeline. We control all five stages — no third-party fill, no white-label.
ISO 20387 · donor consent · COA
Donor screening, raw-material qualification, certificate-of-origin on every input. CellGenic operates under appropriate regulatory frameworks with full compliance, including IND pathways where applicable for products like exosomes.
cGMP-certified · ISO 7
CellGenic manufactures what it sells: the same CellGenic lab characterizes cells, fills vials, signs the COA, and ships the cooler. No white-label, no middlemen — regenerative medicine by CellGenic.
Countries served
MX · AR · CO · PE · US · PA · CR
Verified providers
Batches manufactured
Cleanroom classification
cGMP · ISO 20387
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.
Sterility, endotoxin, mycoplasma, identity, potency. The COA ships in the box and lives in your provider portal forever.
Our protocols are reviewed by practicing physicians in the ten countries we serve. Their notes are how the catalog evolves.
CellGenic operates under cGMP, ISO 7, and ISO 20387. Products are for verified-provider use — not direct-to-consumer sale. Batch traceability and COA ship with every CellGenic order.
CellGenic sells only to physicians, clinic owners, and researchers. Five questions, two minutes — a CellGenic specialist replies within one business day.
Five questions. About two minutes. A specialist follows up within one business day.
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