Sourcing & quality
Know where the material comes from, what the lot documentation records and how the clinical decision is made.
Sourcing
Where the material
comes from
Every peptide is made from raw material imported from the United States, compounded in Asia-based laboratories certified to GMP and HACCP standards, and carries a Certificate of Analysis for its lot.
Lot documentation
Trace the source.
Read the record.
A Certificate of Analysis accompanies each lot. Clinical review and dispensing checks remain separate requirements.
Documentation for each lot
A Certificate of Analysis records results for a particular lot and the tests reported by the issuing laboratory. Read it alongside the product identity, lot number, test methods and specification. It does not, by itself, establish clinical benefit, individual suitability or authorisation for every route of use. Doctor review and dispensing checks remain separate requirements.
The care process
From a request
to a decision
A treatment preference starts a review. It does not guarantee a prescription.
- 01
Questionnaire & request
Health history and treatment preferences form the request. The care model takes payment before doctor review.
- 02
Doctor assessment
A doctor reviews the request and may ask for more information or a consultation before deciding.
- 03
Approval or a full refund
Approval requires a prescription. If a paid request is declined, the entire charged amount is refunded, including any charged delivery, tax and fees.
- 04
Dispensing & delivery
Supply requires a valid prescription and dispensing checks. Further treatment requires fresh review.