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Verification hub

How to verify a stem cell clinic

Eleven short guides that turn marketing claims into checkable facts: certificates, licences, release testing, doses, sources, routes and prices — plus the 25 questions to send before you travel.

Medically reviewed by:
Prof. Dr. Erdal Karaöz Team
Last reviewed:
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The short answer

Verifying a stem cell clinic comes down to six checkable areas: who treats you and where, what the product is, who is licensed to make it, what release testing was performed on your batch, how and why it is being administered, and what the total price covers. Each of those has documents behind it. Ask for the documents by email, before payment, and judge the reply on specificity rather than tone.

Nothing in this cluster depends on choosing us. Apply it to us as readily as to anyone else — that is what it is for.

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How to choose a stem cell clinic in Türkiye: 25 questions to ask before travelling

One email you can send to every clinic on your shortlist, with the reason each question matters and what an acceptable answer looks like.

Open the 25-question checklist

The verification guides

Manufacturing quality

Verify GMP certification

A GMP logo on a website proves nothing. A GMP certificate names an issuing authority, a site address, a scope and an expiry date — and those four fields are checkable.

Read the guide

Regulatory

Verify a cell-processing licence

GMP describes how a facility works. A licence describes what it is legally permitted to do with human tissue — and the two are not interchangeable.

Read the guide

Laboratory documents

Read a Certificate of Analysis

A Certificate of Analysis is the batch's report card: identity, count, viability, sterility, mycoplasma, endotoxin, and the date each test was run. Here is how to read one line by line.

Read the guide

Laboratory documents

Verify cell viability

Viability figures are the most quoted and least qualified number in the industry. A percentage means nothing without the method, the timing and the assay it was measured with.

Read the guide

Laboratory documents

Verify sterility testing

Sterility is the one release test where the honest answer involves a timing problem — and how a clinic explains that problem tells you most of what you need to know.

Read the guide

Laboratory documents

Verify mycoplasma testing

Mycoplasma contamination is invisible: no turbidity, no smell, no change in the culture that you could see. Any expanded cell product must be tested for it specifically.

Read the guide

Comparing offers

Compare cell doses

'100 million cells' sounds like twice as much as fifty million until you ask what was counted, when it was counted, and how many of those cells were alive.

Read the guide

Comparing offers

Compare MSC sources

Wharton's jelly, bone marrow and fat all yield mesenchymal stromal cells, but they differ in donor age, yield, procedure burden and how they behave in culture.

Read the guide

Comparing offers

Compare IV vs intrathecal

The delivery route changes where the cells go, what the procedure risks are, and how strong the supporting evidence is. It is not an upsell decision.

Read the guide

Comparing offers

Compare treatment prices

Two quotes are only comparable once you have reduced both to the same unit: everything actually required, for the same product, at the same dose, including the parts that appear later.

Read the guide

Patient protection

Identify misleading claims

Most misleading marketing in this field is not an outright lie. It is a true sentence about laboratory work presented as if it were a clinical result.

Read the guide

Copy this request and send it to any clinic

Two ready-made messages that ask for the certificates, licences, test results and quotation in one go. Send them unedited, to us as well as to anyone else on your shortlist.

Email template

Subject: Documentation request before consultation — stem cell treatment

Dear team,

I am considering treatment with you and would like to review your documentation before we go further. Please reply by email with the following:

1. The GMP or manufacturing authorisation certificate for the laboratory that will process my cells, showing the issuing authority, site address, scope and expiry date.
2. The licence or registration that permits that facility to procure, process and store human cells, with the licence number and issuing authority.
3. A sample Certificate of Analysis for a released batch, with patient data removed.
4. The release specifications you apply: cell viability, identity markers, sterility, mycoplasma and endotoxin, each with the method used and the acceptance limit.
5. The cell dose I would receive, stated in cells per kilogram of body weight, and the number of doses.
6. The cell source and tissue of origin, and whether the product is autologous or allogeneic.
7. The route of administration proposed for my condition, and the reason for that route.
8. The name and registration number of the physician who would treat me, and the hospital where administration takes place.
9. The published evidence you rely on for my indication, with references.
10. An itemised quotation showing what is included, what is excluded, and your refund policy if I am assessed as unsuitable.

My condition, age and relevant history: [add here].

I understand some answers may depend on assessment. Where that is the case, please say so rather than estimating.

Kind regards,
[your name]
Open in my email app

WhatsApp template

Hello, before booking a consultation I would like to check your documentation. Could you please send me:
1) the GMP certificate for the processing laboratory,
2) the cell-processing licence and its number,
3) a sample Certificate of Analysis,
4) the release limits for viability, sterility and mycoplasma,
5) the cell dose per kilogram and the route of administration,
6) the treating physician's name and registration number,
7) an itemised quotation with exclusions.
Thank you.
Send it to us on WhatsApp

What each answer should contain is explained in the verification guides.

Frequently asked questions

The GMP certificate for the processing laboratory and the Certificate of Analysis format for the product. Those two documents expose more than any conversation, because they either exist with a scope and a signature or they do not.

Not necessarily, but it is unverifiable, and unverifiable is the practical problem you are trying to solve. There is no way for you to distinguish a good unverifiable clinic from a bad one.

Yes. The licensing bodies change by country; the questions do not.

They are produced by our editorial team and medically reviewed by the Prof. Dr. Erdal Karaöz Team, under our published editorial standards and conflict-of-interest disclosure.

Related verification guides

Use this on us too

Send these questions to us exactly as written. We answer them with documents, and if something does not apply to your case we say so.

Ask for the documentation · Back to the verification hub