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

TOPIC

Regulation and Promotion Limits

Advertising for healthcare services is prohibited while non-directive information remains permitted. This topic brings together which phrasing is usable, which content must come down, and how the approval chain should be built.

As regulation narrows, communication does not end; its weight shifts from claim to information. In a field where nobody can use the same claim, the institution that explains best moves ahead.

What is prohibited and what remains permitted

The regulation excludes certificate-based titles, patient-satisfaction content, sponsored and brand-led posts, and discount or campaign announcements.

The permitted space is not small: how the treatment process works, preparation conditions, recovery expectations, institutional identity and team structure can all be described. That is precisely what international patients look for anyway.

The real issue is the approval chain

In most institutions the problem is not ignorance of the rule but ambiguity about who applies it. An image is prepared, marketing approves, a physician objects, legal returns it, and the content waits two weeks.

The concrete output of compliance work is shortening that loop: which content type goes to whose approval within how many working days, and when a physician opinion becomes mandatory.

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Frequently asked questions

What institutions ask about this topic

Which regulation is in force?

The Regulation on Promotion and Information Activities in Health Services, in force since 12 November 2025. Verify the current text from the Official Gazette and Ministry of Health sources.

Does responsibility sit with the agency or the institution?

Before the regulator, responsibility rests with the healthcare institution. Using an agency does not remove it, which is why an internal approval flow is indispensable.

Do the same rules apply to overseas markets?

Complying with Turkish regulation is not enough. The destination market’s own health communication rules, the advertising platforms’ policies and its data protection regime each form a separate filter.

What should we do with our existing content?

Everything published should first pass a risk sweep. Content falling into restricted headings should be taken down and assessed with your legal function.

How long does compliance work take?

Between two and five weeks, scaling with how much is already published. Reviewing the content is the quick part; agreeing who signs off is what stretches the calendar.

What happens when the regulation changes?

The compliance framework is dated and must be reviewed when regulation moves. Working from an out-of-date framework is riskier than having none at all.

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