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Health tourism regulation: a marketing summary

Where the health tourism regulation touches marketing teams: a map of its five chapters and which official text answers which question.

By Roozbeh Nazari · CEO

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Health tourism regulation: a marketing summary

The health tourism regulation is one of the texts clinic marketing teams hear about most and read least. It usually reaches them second-hand: "you can't write that", "you can't use that image". Some of those relayed rules are correct; some have been mixed in from an entirely different piece of legislation. This article sets out where the health tourism regulation stands from a marketing point of view, which chapter concerns promotion, and which questions are in fact answered somewhere else. It is not legal advice; its purpose is to get you to the right text with the right question.

Which text, and where it was published

The regulation's full name is the Regulation on International Health Tourism and Tourist Health, published in the Official Gazette dated 13 July 2017, number 30123. The Health Tourism Department within the Ministry of Health's General Directorate of Health Services announces the text in force and the related regulations on its own pages. The first thing a marketing team needs to know is that the current text should be verified from those two official sources; regulatory texts can be amended over time and blog summaries fall out of date.

We recommend reading the text directly, because the language of the regulation is less heavy than people assume and the chapter headings alone give direction. A marketing manager can read the whole thing in one sitting; the time spent is far below the cost of a campaign that has to be rewritten later.

The five chapters and where marketing sits

The text has five chapters. The first covers purpose, scope, legal basis and definitions. The second regulates international health tourism. The third is given over to tourist health. The fourth chapter is headed pricing, invoicing, information and promotion. The fifth contains miscellaneous and final provisions.

For marketing teams the implication is direct: the provisions concerning promotion are not scattered, but gathered in a single chapter whose heading says so. When a campaign text, a pricing page or a campaign image needs assessing against this regulation, the first place to look is the fourth chapter. That the same chapter is framed together with pricing and invoicing is not accidental either; on the international patient side, price communication and promotion are treated within one frame.

The definitions in the first chapter should not be skipped either. Whether a team's own activity falls inside the regulation is often settled by those definitions: who counts as an international health tourist, which organisation is an intermediary, which activity falls within international health tourism. Teams that proceed on the assumption that they are out of scope end up making the most expensive corrections later.

Authorisation is the precondition for promotion

The regulation's most indirect but most decisive effect on marketing comes through authorisation. International health tourism activity is carried out through authorised health facilities and intermediary organisations, and the Ministry keeps the records of those authorised bodies. The practical consequence: an organisation's ability to present itself as a centre accepting international patients depends first on holding that authorisation. The question to ask before writing the promotional copy is not "how do we word this" but "are we authorised to do this at all". We covered the digital-side implications in our authorisation certificate article.

This point affects website content directly. The targeting done on corporate pages, in language versions and in ad accounts shows which activity you are in fact carrying out. Publishing a landing page aimed at accepting patients in a foreign language is promotion of that activity; the existence of the page and the existence of the authorisation have to be consistent.

The distinction between an intermediary organisation and a health facility also matters for marketing. Their authorisation conditions, and therefore the frame within which they may present themselves, are not the same. Copy from an intermediary that creates the impression it performs the treatment itself is both misleading and at odds with the scope of its authorisation. Clinic and agency teams running joint campaigns need to settle in advance whose voice each sentence speaks in.

Which question sits in which text

This is where teams get confused. The health tourism regulation does not regulate everything; promotion and advertising rules in the health field are the subject of separate legislation, and that legislation has been renewed recently. The question of what a hospital or clinic advertisement may say in general looks there first. The authorisation, definition and price-information frame for international patient activity is the business of this regulation.

A practical routing works like this. "Are we authorised to do this?" — the health tourism regulation and Ministry records. "Can we use this sentence in an ad?" — the current text of health promotion legislation. "How do we display this price on the site?" — the fourth chapter, together with in-house legal opinion. "Can we publish this image?" — promotion legislation and the advertising platforms' own policies. Do not forget that last item; content can comply with the legislation and still be rejected by a platform's policy. We gathered the content-side compliance checks in our medical content guide and the channel plan in our compliant channel plan article.

A working routine for the marketing team

The most reliable way to turn this frame into daily work is to put the approval flow at the start of content production rather than at the end. The arrangement we have seen work: keep a one-page record for every international patient item to be published, stating which activity the content promotes, which authorisation it rests on, and which chapter of which text it was checked against. That record prevents the same questions being reargued at audit time and whenever the team changes.

On multilingual sites the record has to cover the language versions as well. A carefully constructed phrase on the Turkish page can easily become an outcome promise in translation; this is especially common in promotional sentences translated loosely. A compliance check not performed separately for each published language counts as having been performed only in the source language.

Second, the current version of the legislation needs to be tracked from a single place. Because regulatory texts can be amended, an internal decision taken a year ago may no longer hold today. Following the official source directly is cheaper than trusting second-hand summaries. You can find what our clinic-side work covers on our clinics page and our sector work as a whole on the industries page.

One last reminder: nothing described here is a substitute for legal advice. This summary was written to make it easier to go to the right text with the right question; what binds you is the official text in force and your organisation's legal opinion. On any sentence you are unsure about, the default should be to ask the legal team rather than publish; withdrawing a promotional text always costs more than asking before it goes out.

Sources

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