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Germany

2 dated sources Reviewed 2026-08-20 Next review 2026-11-18

Germany applies the Arzneimittelgesetz alongside anti-doping legislation, and sets criminal thresholds for named peptide substances. Classification follows intended use and presentation rather than product description.

Buyers in this market search for: Peptide Grosshandel, Private Label Peptide, Peptid Lieferant.

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The regime

How compounds are classified in Germany

Governing lawThe Arzneimittelgesetz (medicines act) is the primary regime, alongside the Anti-Doping-Gesetz and, for some substances, the Betaeubungsmittelgesetz. Import and customs rules apply on top.
What determines classificationIntended use, presentation, form and pharmacological effect. The description applied at the point of sale does not by itself determine which regime applies.
Named-substance thresholdsThe Dopingmittel-Mengen-Verordnung, in force since March 2023, sets specific quantity thresholds for named peptide doping agents. Above those thresholds the exposure is criminal rather than administrative.
Prescription-only compoundsSomatropin and the gonadotropins are prescription medicines. Supply outside a prescription route is not lawful regardless of how the product is described.
Enforcement postureActive. German customs screens inbound shipments and refers cases to prosecutors, including on consignments originating inside the EU. Published enforcement has focused on commercial-scale supply rather than individual purchasers.
Already supplying Germany? Send the compounds and volumes you buy today and we will quote against them.Send your list

Your obligations

What a buyer in Germany needs settled

  • Confirm which regime each compound falls under before ordering, per compound, not per order.
  • Hold the wholesale or import authorisation your intended activity requires.
  • Retain the batch certificate against the batch, since customs enquiries reference consignments.
  • Do not rely on product descriptions to establish classification.

We will ask about this at enquiry. We check the authorisations your activity requires before quoting, and we confirm the position per compound rather than for the market as a whole.

Sources

Check this yourself

Every position above traces to a dated public document. The authority, the document, the date and the link are below.

Authority and documentDateLink
BfArM
Press warning on Melanotan-containing products
2010www.bfarm.de/SharedDocs/Pressemitteilungen/DE/2010/pm14-20...
Zoll (German customs)
Press release on a doping-substance investigation
2025www.zoll.de/SharedDocs/Pressemitteilungen/DE/Sonstiges/202...

Links go to the issuing body wherever one exists. Positions change. If you are relying on any of this, check the source rather than this page.

Market brief

Take the Germany brief as a PDF

The regime, the buyer obligations and all 2 sources, dated and linked, in one document you can forward.

Nearby

German-speaking markets and nearby markets

Buyers supplying one of these usually supply the others. The requirements are not the same.

CodeMarketSources
ATAustria3 sourcesBASG has published a dedicated position holding that a research-use label does...
CHSwitzerland5 sourcesSwissmedic regulates therapeutic products under the Heilmittelgesetz and runs ...
NLNetherlands3 sourcesThe IGJ and the NVWA assess offerings jointly and have stated their position o...
PLPoland2 sourcesGIF and GIS have issued a joint public warning on synthetic peptides offered a...

Scope

How to use this page

A summary of the published regulatory position in Germany as at 2026-08-20, written for procurement teams deciding how to source. Every source is dated and linked so it can be checked at origin.

It is not legal advice. Full terms of supply, including where responsibility sits, are set out in our terms of supply.

Questions

Supplying into Germany

Do you supply into Germany?

We supply businesses that hold the authorisations their activity requires. Whether a specific compound can be supplied into Germany depends on that compound and on your authorisations, and we confirm it per compound at the enquiry stage.

Who carries the compliance obligation?

The importer of record and the party placing the product on the market, which is the buyer. We supply the batch documentation that supports your file. We cannot hold your authorisations for you.

How current is this page?

It was reviewed on 2026-08-20 and is scheduled for review again on 2026-11-18. Every source is dated and linked, so you can check the original.

We already supply into Germany. What changes if we source from you?

The batch documentation. You receive a Certificate of Analysis per batch, which can be issued under your own brand. The import and market-placing responsibilities stay where they are.

Is this legal advice?

No. It is a summary of the regulatory positions those authorities have published, as at the review date above. Take advice in your own market before you rely on it.

Enquire about supply into Germany

Tell us the compounds and your authorisations. We confirm per compound before anything ships.

Anything else you already know. All optional.

We supply businesses across the EU, and we reply within one working day.