What the public record says
The Australian Register of Therapeutic Goods, ARTG, is the public register for therapeutic goods that can be supplied in Australia. Buyers should use it to check product name, sponsor, active ingredients, dosage form, warnings, start date, and whether the product is listed, registered, included, or export-only. A research peptide storefront should not be treated as approved unless the exact product record supports that claim.
What buyers should check
- Ask for the AUST R, AUST L, or ARTG identifier when a seller uses approved, registered, listed, or TGA language.
- Search the exact product name, sponsor, and active ingredient in the ARTG, not just the vendor's brand name.
- Check whether the dosage form and active ingredient match the vial, capsule, nasal spray, or compounded product being sold.
- Do not treat an approved ingredient, overseas approval, or a lab COA as Australian product approval.
- If a clinic or supplier uses pharmacy or compounding language, check the prescribing, dispensing, compounding, and advertising path separately.
- If the seller cannot provide an ARTG pathway, the page should say evidence pending rather than turning approval language into proof.
Source links
Use this regulatory brief to ask better supplier questions. Do not convert a market-level warning into a vendor-specific claim unless the vendor page has a source attached.
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