Remote service for eligible medical-tourism organisationsTürkiye · Europe · Dubai/Gulf

Medical-tourism guide

Regulation and Compliance

Advertising for healthcare services is prohibited; information is permitted. The regulation of 12 November 2025 bars explicit and implicit advertising while allowing information given by authorised health professionals without direction.

Sağlık Ajansı editorial teamLast reviewed:

This guide describes the practical communication consequences of the regulation. It is not legal opinion and should be assessed with your institution's legal function.

The health promotion regulation shown with its permitted and prohibited areas
The health promotion regulation shown with its permitted and prohibited areas

Separating the prohibited from the permitted

The regulation prohibits certificate-based titles, patient-satisfaction content, sponsored and brand-led posts, discount and campaign announcements, and promotion contrary to personal data protection law.

The permitted area is information consistent with the practitioner's field and with scientific and ethical principles. How the treatment process works, preparation conditions, recovery expectations, institutional identity and team structure can all be described.

Content types treated as prohibited in practice

  • Patient reviews, satisfaction posts and thank-you messages
  • Before-and-after imagery and outcome comparisons
  • Discount, campaign and package price announcements
  • Certificate-based title usage
  • Sponsored and brand-led health posts
  • Comparative superiority claims

Enforcement and responsibility

Breach can lead to administrative sanction, access blocking, sanctions under personal data protection law and, where applicable, criminal process.

Responsibility rests with the healthcare institution. Using an agency or a supplier does not remove it, which is why an internal approval flow is the most effective practical protection.

Building a compliant approval flow

The working model has three steps: assign an approver by content type, set a maximum turnaround for each approver, and record rejected phrasing.

Over time the rejected-phrase record becomes an institutional glossary and prevents the same errors recurring. It is the most practical way to lower compliance cost.

01

Advertising prohibited

Explicit and implicit advertising barred; non-directive information permitted.

02

Responsibility is institutional

Using an agency does not remove it; an approval flow is essential.

03

Two filters

Turkish regulation and destination-market rules apply separately.

Working sequence

How we move, step by step

  1. 01
    Content sweep

    All published content flagged for risk.

  2. 02
    Bucket separation

    Permitted, conditional, prohibited and uncertain phrasing separated.

  3. 03
    Institutional glossary

    Preferred and rejected phrasing written with reasons.

  4. 04
    Approval flow

    Role-based chain and turnaround commitment defined.

  5. 05
    Periodic review

    The framework refreshed when regulation changes.

Frequently asked questions

What institutions ask most about this

Can we post nothing on social media now?

You can. Process narrative, preparation information, institutional and team introductions and informative content remain permitted. Directive, claim-bearing and satisfaction-based content is restricted.

Should we remove patient reviews from our site?

Patient-satisfaction content is among the restricted headings. We recommend removing it from publication and assessing the position with your legal function.

Can we run Google advertising?

Platform policies and Turkish regulation must be assessed together. Information-led structures without claims are safer for both approval and compliance.

How real is the enforcement risk?

Administrative sanctions, access blocking and data protection penalties are set out in the regulation. Treating the risk as concrete and working preventively is the sensible approach.

Does an agency share responsibility?

An agency may carry contractual responsibility to you, but responsibility before the regulator sits with the healthcare institution. That is why an internal approval flow is indispensable.

How often does the regulation change?

Health communication regulation has been updated several times in recent years, which is why framework documents must be dated and reviewed periodically.

Next step

Let us sweep your content against the regulation

Share your published content and we will start with the risk sweep.

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