Health Tourism Regulatory Compliance

We advise hospitals, clinics and health tourism intermediaries on the authorisation certificate regime introduced by the Regulation of 26 April 2025: the application file, the accreditation and certification deadline, the Portal and record-keeping duties, the advertising ceiling, and the defence of a suspension, a revocation or an administrative fine.

Av. Onur ÇalışıcıIstanbul Bar reg. no 83426 · Updated October 2026

In brief

  1. Article 5(1) of the International Health Tourism Regulation makes an authorisation certificate compulsory and splits the issuing power: the Ministry of Health certificates the health facility, USHAŞ the intermediary organisation; the certificate cannot be transferred (Article 5(5)), and a second intermediary office or branch needs its own certificate before it may operate (Article 5(4)).
  2. Hospitals, medical centres, medical laboratories and dialysis centres must be accredited by TÜSKA; other facilities must hold a Ministry certificate. Provisional Article 1(3) sets 31 December 2026 for that obligation.
  3. The words 'complication and' in the shared-responsibility rule in Article 6(3) are annotated on the consolidated text as stayed (yürütmeyi durdurma); the complication insurance rule in Article 6/1(c) carries no stay note.
  4. Responsibility between facility and intermediary is allocated by the type of service supplied; Article 6(3) does not create joint and several liability.
  5. A fine issued under Additional Article 11 of Law No. 3359 is challenged before the magistrate's court in criminal matters within 15 days, but goes to the administrative court where an administrative-law decision was issued in the same act (Article 27(8) of Law No. 5326).

Serving international patients in Türkiye is a licensed activity, not an extension of an ordinary hospital or clinic licence. Article 5(1) of the International Health Tourism and Tourist Health Regulation, published in the Official Gazette of 26 April 2025 (No. 32882), makes an authorisation certificate compulsory before a health facility or an intermediary may operate in this field, and splits the issuing power in the same sentence: the Ministry of Health certificates the facility, USHAŞ certificates the intermediary. Accreditation, records, pricing, advertising, inspection and sanctions all sit on top of that one requirement.

Two Authorisations, Two Authorities, Two Files

The Regulation draws its authority from Article 9(c) and Additional Articles 11 and 19 of Law No. 3359, the Fundamental Law on Health Services, among others. The statute reaches this sector expressly: the first paragraph of Additional Article 11 states that all acts and transactions relating to the provision of health services are inspected by the Ministry of Health, and the following sentence adds that this also covers the activities of every kind of organisation within the scope of international health tourism.

Read the full section

Under Article 4(1)(a), an intermediary is an undertaking operated by certificated legal persons (which rules out a sole trader holding the certificate) that advises the patient and companions and arranges the facility, accommodation, transport and transfers. Under Article 4(1)(e), a facility is one holding both a licence under its own legislation and a Ministry authorisation certificate. Two definitions, two authorities, two application files. Our companion note sets out the authorisation certificate procedure end to end, including refusal and revocation.

Stage Health facility (Art. 5(2)) Intermediary (Art. 5(3))
Where the application is filed Through EKİP, with the Annex 1/A documents To USHAŞ, with the Annex 1/B documents
Who reviews it Provincial or district health directorate USHAŞ
Notice of a deficiency Within 15 working days Within 15 working days
Period to cure it 30 working days, failing which the application is deemed refused 30 working days, failing which the application is deemed refused
On-site inspection Inspection team formed by the directorate; suitable files sent to the Ministry within 15 working days Inspection team formed by USHAŞ
Certificate issued Annex 3/A, by the Ministry, within 15 working days of approval Annex 3/B, by USHAŞ, within 15 working days

Two further rules shape corporate planning. Article 5(5) provides in a single sentence, with no qualification after it, that the certificate cannot be transferred, so an acquisition structured as an asset purchase does not carry the authorisation across. Article 5(4) requires a separate certificate for each additional intermediary office or branch opened by the same owning legal person, and bars health tourism activity in an office not authorised that way.

The Service Standards a Certificate Presupposes

Article 6(1) sets the facility standards. Sub-paragraph (b) requires hospitals, medical centres, medical laboratories and dialysis centres to hold TÜSKA accreditation, and other health facilities to obtain the Ministry certificate: one obligation, two routes, decided by the kind of establishment. Provisional Article 1(3) allows until 31 December 2026 for that duty. Provisional Article 1(1) is a separate clock and has already run: a facility or intermediary that already held a health tourism certificate when the Regulation entered into force had six months from that date to bring itself into line, and the certificate of one that did not is revoked.

Read the full section

Sub-paragraph (ç) confirms that a facility may accept a patient who applies directly; there is no compulsory intermediation. Sub-paragraph (d) permits remote health services within the framework of the Regulation on the Provision of Remote Health Services of 10 February 2022 (No. 31746), announced through the Portal. Sub-paragraph (e) is the clause that most often needs contractual work: a facility may not procure, from persons or organisations without an authorisation certificate, services that are to be performed by an intermediary. That turns every referral arrangement into a due-diligence question.

Article 6(2) governs the intermediary. Accommodation, transport and transfer must go through travel agencies licensed under Law No. 1618, and the next sentence carries the exception that changes the structure of many groups: those services may be carried out by the intermediary itself where the intermediary is a licensed travel agency. The intermediary must also hold, or contract in, a call capability in at least two foreign languages, seven days a week and 24 hours a day, and its personnel may not work at more than two intermediaries at once. How those duties meet the facility’s own is the subject of our note on the legal position of health tourism intermediaries, including the allocation of responsibility by type of service under Article 6(3).

Inside the facility, Article 7 requires an international health tourism unit covering admission, registration, diagnosis, treatment, invoicing, discharge, interpreting and coordination with intermediaries; at least one staff member must have a foreign language, documented; staff details go to the health directorate through EKİP; and a named responsible officer is assigned to each patient and recorded on the Portal.

Records, Pricing, Invoicing and the Advertising Ceiling

Article 8 requires a health information system registered with the Ministry, processing of personal health data in accordance with the Personal Data Protection Law No. 6698 and Additional Article 19 of Law No. 3359, and its transfer to the central health data system under procedures set by the Ministry (the wider duties are on our personal data protection page), and requires facilities and intermediaries to join the Portal and keep entries complete, accurate and current. Article 8(5) extends the notification duty to all service units established abroad, not only those in Türkiye.

Read the full section

This is where the statute bites. Additional Article 11(3) of Law No. 3359 subjects a health institution that fails to keep the records determined by the Ministry, or to comply with a notification obligation, to an administrative fine expressed as a floor amount and, above it, a percentage of the previous month’s gross service revenue. Article 17(7) of the Misdemeanours Law No. 5326 increases administrative fines at the start of each calendar year by the revaluation rate, but its final sentence states that the rule does not apply to proportionate fines. Because these fines combine a fixed floor with a percentage of revenue, the figure to apply should be checked for the year concerned rather than read off the statute.

On price, Article 11 provides that the fee for a health service supplied within international health tourism is determined by the Ministry, and obliges the facility to comply with the procedures and principles in the Ministry’s health tourism tariff; the tariff in force at the time governs and should be checked directly. Article 12 requires a sales receipt or invoice with an annexed itemised breakdown and unit prices, plus certain documents free of charge on request: medicines and consumables charged to the patient, laboratory and imaging results (forensic originals excepted), and outside prescriptions; the intermediary must itemise accommodation, transport, transfer, interpreting and consultancy fees.

On promotion, Article 13(2) requires a website with a foreign-language option, requires the organisation name and titles on it to match the title and ownership name on the authorisation certificate, and requires the facility to publish its accreditation certificate or certificate there. The statutory ceiling sits in the paragraph added to Additional Article 11 of Law No. 3359 on 21 July 2025: a private health organisation may not engage in activity in the nature of advertising that exceeds the limits of promotion and information, and the permitted content is listed exhaustively: address and contact details, working days and hours, the specialty branches in which patients are accepted, the professional and academic titles of the health professionals employed, and health-protective and health-promoting information related to the field of service. Exceeding that, or acting misleadingly or deceptively, carries an administrative fine.

The Stayed Wording in Article 6(3)

One part of the Regulation is currently annotated as stayed (yürütmeyi durdurma) on the consolidated text published by mevzuat.gov.tr:

  • The words “complication and” in Article 6(3), so that responsibility for post-treatment events currently reads as extending to medical malpractice while the complication limb is suspended.
Read the full section

Article 6/1(c), the requirement that the facility take out complication insurance for surgical and interventional procedures performed in an operating theatre, carries no stay note, and the 31 December 2025 date that Provisional Article 1(2) set for that duty has passed.

A stay of execution is not an annulment, and the merits are decided separately. On attacking a regulation, Article 7(4) of Law No. 2577, the Administrative Procedure Law, runs the period from the day after publication, but the same paragraph continues that on the application of such an act those concerned may sue against the regulatory act, the applied act, or both, and that the regulatory act not having been annulled is no obstacle to annulling the act based on it.

The compulsory professional financial liability insurance for physicians is a separate matter and was not affected. Under Additional Article 12 of Law No. 1219, the Law on the Practice of Medicine, that cover is taken out by the private health institution for those working in it, half the premium is paid by the employer, and the following sentence bars deducting the employer’s half from the employee’s salary or other financial entitlements under any name or in any manner, and bars any contract clause providing for it. We set the two covers side by side in our note on complication insurance and physician liability insurance.

Inspection, Suspension, Revocation and the Route of Challenge

Article 15 applies the Regulation on the Inspection of Private Health Facilities of 17 November 2023 (No. 32372) and the criteria in Annexes 4 and 5. It carries a consequence that is easy to miss: a facility or intermediary whose activity is stopped, or whose certificate is suspended or revoked, is reported by the Ministry to the Ministry of Trade and to the Ministry of Culture and Tourism.

Trigger Consequence Source
Performance assessed as partly sufficient, not cured at the control assessment Certificate suspended for 3 months Art. 9(2)(a)
Performance assessed as insufficient, not cured at the control assessment Certificate suspended for 6 months Art. 9(2)(b)
Second control assessment still not passed Certificate revoked Art. 9(2)
Urgent situation endangering the patient's health or safety Certificate suspended until that situation ends Art. 16(2)
Records kept improperly 6-month suspension; revocation if repeated within one year Art. 16(3)
No health tourism activity in the past year Certificate revoked Art. 16(4)
Certificate revoked No new certificate for one year Art. 16(5)
Fine under Add. Art. 11 repeated within one year Fine doubled; on a third instance, activity stopped for up to ten days Law No. 3359, Add. Art. 11
Read the full section

Note the limit that follows the escalation rule in Additional Article 11: where there is more than one health institution under the same name and ownership, the sanctions apply only to the institution at which the breach occurred. The same article separates the deciding authorities: governors impose the fines, the Ministry of Health orders the stoppage of activity.

The forum has to be identified first, because the routes differ. An annulment action against a refusal, suspension or revocation runs on the 60-day period in Article 7(1) of Law No. 2577, from the day after written notification under Article 7/2(a). A pre-action application to the superior authority under Article 11 stops the clock, and silence for thirty days counts as a refusal. The trap is in the third paragraph: when the period restarts, the time that ran before the application is counted in. It does not reset. Filing does not by itself suspend the decision (Article 27(1)), and a stay requires both irreparable harm and manifest unlawfulness (Article 27(2)). An administrative fine standing alone follows a different route under Law No. 5326 (fifteen days to the magistrate’s court in criminal matters), while Article 27(8) sends the unlawfulness arguments to the administrative court where administrative-law decisions were issued about the same person in the same act.

The Regulation does not itself name the forum for a decision taken by USHAŞ, which is constituted as a joint-stock company and issues and suspends intermediary certificates under Articles 5(1) and 16(2). Where an intermediary’s certificate is refused, suspended or revoked, that question is worth settling before a time limit runs.

Our Approach

We work from the text of the Regulation and the statute behind it rather than from sector practice, because the sanctions attach to the text. A file usually starts with a gap analysis against Articles 5 to 13, moves to the contracts that carry the risk (the intermediary agreement, the travel-agency chain, the physician engagement and its insurance clause) and ends with the documentation an inspection under Annexes 4 and 5 will ask for. Where a decision has already been taken, we work backwards from the time limit. Patient-side malpractice claims are a different subject, dealt with on our medical malpractice and healthcare regulation page.

Key figures

Art. 5(1)
Authorisation certificate compulsory; Ministry for facilities, USHAŞ for intermediaries
15 / 30 working days
Notice of a deficient application, then the period to cure it
31.12.2026
Deadline in Provisional Article 1(3) for the accreditation and certification duty
60 days
Time limit for annulment proceedings under Article 7 of Law No. 2577

How we run a health tourism compliance file

  1. Map the entity against the definitions

    Article 4 defines a facility as one holding both a licence under its own legislation and a Ministry authorisation certificate, and an intermediary as an undertaking operated by a certificated legal person. We establish which definition an organisation falls into before anything else, because the two follow different authorities and different files.

  2. Build the application file

    The facility applies through EKİP with the documents in Annex 1/A; the intermediary applies to USHAŞ with those in Annex 1/B. We assemble the file so that the deficiency notice under Article 5 does not start a cure period that can lapse.

  3. Close the standards gap

    Accreditation or certification, the international health tourism unit and its documented language capacity, the health information system registered with the Ministry, the two-language round-the-clock call capability for intermediaries, and the foreign-language website required by Article 13(2).

  4. Fix the contract chain

    Article 6/1(e) bars a facility from buying intermediary-type services from an unauthorised provider, and Article 6/2(a) routes accommodation, transport and transfer through licensed travel agencies. We redraft the agency, referral and physician contracts so the chain matches the Regulation.

  5. Defend inspections and sanctions

    We handle the inspection response, the performance re-assessment under Article 9, and the challenge to a suspension, a revocation or a fine, including the choice of forum, which is not the same for every decision.

Frequently asked questions

Who issues a health tourism authorisation certificate in Türkiye, and can a hospital licence stand in for it?

No. They are two separate documents. Article 4/1(e) of the Regulation defines a health facility as an establishment that both holds a facility licence under its own legislation and has been issued an authorisation certificate by the Ministry. Article 5(1) then states that a certificate is compulsory before a facility or an intermediary may operate in international health tourism, and splits the issuing power in the same sentence: the Ministry of Health for the health facility, USHAŞ for the intermediary. An operating licence, an accreditation certificate and an authorisation certificate are three different things, and only the last one opens the health tourism activity.

How long does the application take, and what happens if the file is incomplete?

The Regulation sets working-day periods rather than a total processing time. A facility applies through EKİP with the Annex 1/A documents; the provincial or district health directorate reviews them and, if it finds a deficiency or a failure to meet the criteria, notifies the applicant within 15 working days. The consequence is stated in the next sentence of Article 5/2(a): an applicant who cannot complete the missing items within 30 working days is deemed to have had the application refused. If the file is clean, an on-site inspection follows, suitable applications are sent to the Ministry within 15 working days, and the Ministry issues the Annex 3/A certificate within 15 working days of approving them. Article 5(3) runs the same clocks for an intermediary applying to USHAŞ, ending in the Annex 3/B certificate.

Can a certificate be sold with the clinic, or extended to a second office?

Article 5(5) is one sentence long and admits no exception: the international health tourism authorisation certificate cannot be transferred. That has a direct effect on how a clinic or an intermediary is bought: a share transfer and an asset transfer are not equivalent here, and the acquirer needs to know before signing which side of that line the deal falls on. Article 5(4) deals with expansion: where the legal person owning an intermediary wants to open a second intermediary or a branch, a new certificate is required for each one, and health tourism activities may not be carried on in a second office or branch that has not been authorised in that way.

Is TÜSKA accreditation compulsory for every facility?

The obligation is compulsory but not uniform. Article 6/1(b) requires hospitals, medical centres, medical laboratories and dialysis centres to be accredited by TÜSKA, and requires health facilities other than those to obtain the certificate issued by the Ministry. So the question is not whether to comply but which of the two routes applies to the establishment. Provisional Article 1(3) gives facilities until 31 December 2026 for that obligation.

Was the complication insurance obligation actually withdrawn?

No. The consolidated text on mevzuat.gov.tr carries one stay in the body of the Regulation, and it is not on that obligation: it covers the words 'complication and' in Article 6(3). Sub-paragraph (c) of Article 6(1), which requires a facility to take out complication insurance for surgical and interventional procedures performed in an operating theatre, carries no stay note, and the 31 December 2025 date that Provisional Article 1(2) set for that duty has passed. The two insurances and who pays for them are set out in our note on complication insurance and physician liability insurance.

Does the Regulation make the clinic and the intermediary jointly liable to the patient?

It does not say that. Article 6(3) provides that the facility and the intermediary are responsible for the health services and intermediary services the international health tourist receives while in Türkiye 'depending on the type of service supplied', and adds that medical malpractice arising after the health service is within that responsibility. The criterion is the type of service, not a shared pool of liability, and the word 'complication' in that sentence is currently stayed. The allocation between the two, and the general contract rules that fill what the Regulation leaves open, are examined in our note on the legal position of health tourism intermediaries.

A fine has arrived. Which court hears the objection?

That depends on what else was decided in the same act. Administrative fines under Additional Article 11 of Law No. 3359 are imposed by governors, and Article 27(1) of the Misdemeanours Law No. 5326 sends such a decision to the magistrate's court in criminal matters within 15 days of service or pronouncement, and the same paragraph adds that if no application is made in that period the decision becomes final. But Article 27(8) redirects the file: where decisions falling within the jurisdiction of the administrative courts have also been issued in respect of the same person within the same act, the unlawfulness arguments against the fine are heard together with the annulment claim in the administrative court. A fine on its own goes one way; a fine issued in the same act as a decision that belongs to the administrative courts goes the other.

This page is general information, not legal advice. For advice on your specific situation, speak with a lawyer.

Av. Onur Çalışıcı

The lawyer on your file

Av. Onur Çalışıcı

Founding Attorney · Istanbul Bar Association · Bar reg. no 83426

Lex lata is Latin for “the law as it is”. The office was founded by Av. Onur Çalışıcı, and you deal with Av. Çalışıcı directly from the first meeting to the end of the matter. With foreign clients we write in English and explain what each Turkish document says.

Write to us with what happened and which documents you have. We will read it and get back to you. You can write in English or Turkish.

Last reviewed: October 2026 · LinkedIn: linkedin.com/in/onurcalisici

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