GMP (Good Manufacturing Practice)
An internationally recognised standard for the safe, sterile, reproducible production of biological and pharmaceutical products.
Lab & Quality
What is GMP (Good Manufacturing Practice)?
Good Manufacturing Practice (GMP) is the international quality framework that governs the production, testing and release of pharmaceutical and biological products — including human cell therapy. GMP-certified facilities operate under strict environmental monitoring, validated cleanroom classifications (typically ISO Class 7 or better for cell processing), documented operator training and lot-by-lot release testing for sterility, endotoxin, mycoplasma, viability and identity. TurkeyStemcell sources Wharton's Jelly MSCs exclusively from licensed GMP facilities audited by the Turkish Ministry of Health.
Related terms in Lab & Quality
Cell Passage
How many times a stem cell population has been expanded in culture. Lower passages (P2–P5) are clinically preferred.
Potency Assay
A pre-release laboratory test that confirms a cell batch's biological activity — not just cell count.
ISCT MSC Criteria
The 2006 International Society for Cell & Gene Therapy definition that all clinical MSCs must meet.
Have a clinical question about your case?
Our medical coordinators answer in plain English before you book anything.
Or call directly: +90 534 856 92 92