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Peptide supply requirements in 25 EU markets.

Click a country for the regulator, the published position, and every source dated and linked.

25 markets 78 dated sources Reviewed 2026-08-20
MarketSourcesSummary
Austria AT3 sourcesBASG has published a dedicated position holding that a research-use label does not change a peptide's cl...
Belgium BE3 sourcesBelgium applies EU medicines law through the FAGG, which has published a GLP-1 warning. No dedicated pos...
Bulgaria BG5 sourcesThe BDA regulates under the national medicines law and participates in the EU counterfeit-GLP-1 warning ...
Croatia HR1 sourcesHALMED has published a general rule on online medicine sales. No notice naming research-labelled peptide...
Czechia CZ2 sourcesSUKL holds that most synthetic peptides meet the functional definition of a medicinal product, so classi...
Denmark DK5 sourcesLaegemiddelstyrelsen maintains standing warnings, including on Melanotan. Research-chemical framing is a...
Estonia EE2 sourcesRavimiamet published a dated statement in June 2026 addressing internet-sold peptides marketed for resea...
Finland FI2 sourcesFimea has warned against injectable peptides sold through social media. Semaglutide is a prescription me...
France FR3 sourcesANSM names compounds individually in its public alerts and has issued sanitary-police decisions against ...
Germany DE2 sourcesGermany applies the Arzneimittelgesetz alongside anti-doping legislation, and sets criminal thresholds f...
Greece GR4 sourcesEOF issued a public warning in July 2026, and related reporting names specific compounds. Regulatory att...
Hungary HU5 sourcesOGYEI regulates medicines under Act XCV of 2005. A case-by-case research permit exists for controlled su...
Ireland IE2 sourcesThe HPRA detained 763,027 dosage units of falsified or unauthorised medicines in 2025. Ireland is Englis...
Italy IT1 sourcesAIFA regulates under the Codice del farmaco and has warned on illegal GLP-1 supply through unauthorised ...
Latvia LV4 sourcesThe ZVA regulates under the Farmacijas likums and has published dated GLP-1 safety communications. No pe...
Lithuania LT4 sourcesThe VVKT regulates under the Farmacijos istatymas and requires a wholesale distribution licence. No posi...
Netherlands NL3 sourcesThe IGJ and the NVWA assess offerings jointly and have stated their position on research-use framing dir...
Poland PL2 sourcesGIF and GIS have issued a joint public warning on synthetic peptides offered as chemical reagents. The P...
Portugal PT5 sourcesINFARMED governs medicines under the Estatuto do Medicamento and has flagged a rise in illegal online su...
Romania RO3 sourcesANMDMR operates under the EU medicines framework and has publicly identified a fraudulent tirzepatide pr...
Slovakia SK3 sourcesSUKL named BPC-157, ipamorelin and melanotan directly in a July 2025 press release tied to an INTERPOL o...
Slovenia SI2 sourcesJAZMP published a dated warning on injectable peptides in April 2026 and names semaglutide and somatropi...
Spain ES2 sourcesAEMPS has issued a formal notice on illegal GLP-1 supply and directs buyers to verify pharmacies through...
Sweden SE5 sourcesLakemedelsverket has a published position on Melanotan II, and a government-commissioned report quantifi...
Switzerland CH5 sourcesSwissmedic regulates therapeutic products under the Heilmittelgesetz and runs a named, active cross-agen...
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How to read these

Every position is sourced and dated

Each market page names its regulator, carries a review date, and lists every source with a link to the issuing body, so any statement on it can be checked at origin.

Twenty-five markets, seventy-eight dated sources. This is the reference we use ourselves when a buyer asks whether a compound can be supplied into their market. It is published so the answer is available before you ask for it.

Reviewed 2026-08-20, next review 2026-11-18. Not legal advice; full terms of supply are set out in our terms.