The Science Library

How cell and exosome biologics are made, measured and documented, written for licensed practitioners who want to evaluate a supplier on evidence.

Last updated October 7, 2026For licensed medical professionals4 peer-reviewed and regulatory sources

In short

The Science Library explains the manufacturing and testing behind biologics: 3D bioreactor culture, population doublings and passages, why umbilical cord tissue is used as an MSC source, and how exosomes are produced and counted. Every page cites peer-reviewed or regulatory sources and ends with the questions to ask any supplier.

Start with a topic

Standards and documentation

How these pages are written

  • Process, not promises. We write about how products are made and measured, not what they do in the body.
  • Cited. Every factual claim about culture, sourcing or measurement links to a peer-reviewed paper or regulation.
  • Practical. Each page ends with questions you can put to any supplier, including us.
  • Dated. Pages show a last-updated date and are revised as guidance changes.

Frequently asked questions

Who is the Science Library for?

Licensed medical professionals (MD, DO, NP, PA) evaluating cell and exosome suppliers, and their teams.

Do these pages make claims about patient results?

No. They cover manufacturing, characterization and sourcing. Exosome products are topical cosmetic products; hUCT-MSC products are individualized and not FDA-approved.

Where can I see lot documentation?

See Documentation & COAs, or contact our team to request a lot's paperwork.

References

  1. Dominici M, Le Blanc K, Mueller I, et al. Cytotherapy. 2006;8(4):315-317. doi:10.1080/14653240600855905. Cited for: ISCT minimal criteria for defining MSCs.
  2. Welsh JA, Goberdhan DCI, O'Driscoll L, et al. J Extracell Vesicles. 2024;13(2):e12404 (MISEV2023). doi:10.1002/jev2.12404. Cited for: EV nomenclature and characterization guidance.
  3. Wagner W, Horn P, Castoldi M, et al. PLoS One. 2008;3(5):e2213. doi:10.1371/journal.pone.0002213. Cited for: replicative senescence across passages.
  4. U.S. Code of Federal Regulations, Title 21, Part 1271: Human Cells, Tissues, and Cellular and Tissue-Based Products. eCFR. Cited for: cGTP and donor eligibility requirements.

Citations support manufacturing, characterization and sourcing facts only. They are not claims about any Stem Nova product's effect in the body.

Source with the paperwork in hand

Licensed MD, DO, NP and PA practices can apply for wholesale access. Lot documentation is available for review, and applications are typically approved within 24 hours.