Quality & Compliance
What you receive, and what remains yours to determine.
This page is written to be read carefully. It sets out our documentation, our testing cadence, and the limits of our responsibility.
Documentation package
Each consignment ships with a complete file. Nothing is issued after the fact, and nothing is summarised on our letterhead in place of the original record.
- Certificate of analysis
- Issued per batch and identified by lot number. Covers the parameters agreed in the specification.
- Third-party test report
- Independent verification from [named laboratory], reported against the same specification.
- Specification sheet
- The written standard the batch was produced and released against.
- Chain-of-custody record
- Handling record from production release through consolidation to consignment.
- Packing list and shipping documents
- Commercial invoice, packing list, and export paperwork prepared before dispatch.
- Storage and handling sheet
- Stated storage conditions, including temperature range where [applicable].
Testing cadence
Per batch
Identity, appearance, and purity checks by the manufacturing partner, with a COA issued on release.
Per [nth] batch
Independent third-party verification against the same specification.
Annually
Facility re-review, document audit, and confirmation of approved production scope.
On change
Re-qualification whenever a partner changes process, site, or material source.
Regulatory responsibility
Classification differs by market.
How a peptide product is classified — and what may lawfully be said about it — varies between jurisdictions. A classification that applies in one market does not carry to another. Import permits, licensing, labelling requirements, and permitted claims are determined by the destination market.
Well Bali supplies products with their production and testing documentation. We do not advise on regulatory status, and we do not make health or performance claims about any product we supply. Buyers are responsible for determining classification, obtaining any required authorisations, and ensuring their own labelling and marketing comply with the law where they operate.
Where a buyer's artwork or copy reads as a claim we cannot support with the documentation on file, we will say so before production.
Products are supplied to qualified commercial buyers for lawful use in their own market. Nothing in our materials constitutes medical advice or a therapeutic claim.
Ask to see a sample documentation package.
We share a redacted example with qualified buyers under a mutual confidentiality agreement.