What goes on the shelf,
and what doesn't.
Our standard is simple: if a compound wouldn't pass our own laboratory protocols, it doesn't enter our catalog. This page documents how we source, screen, verify and dispatch every product — and how to read the data we publish for each batch.
The four-stage
quality pipeline.
Every vial that leaves our facility has cleared four sequential stages — and the data from each stage is auditable on its Certificate of Analysis.
GMP-aligned manufacturers only. No grey-market, no resellers, no rebrands. Every supplier runs a 90-day evaluation before a single SKU enters the catalog.
Every batch is shipped to an accredited third-party UAE laboratory for HPLC purity, mass-spec identity, and endotoxin screening — before it ever reaches the catalog.
Each verified batch is locked to a unique identifier and a public Certificate of Analysis. If the COA doesn't pass, the batch doesn't ship.
Plain, unbranded, tamper-evident packaging. UAE-wide dispatch within 48 hours with full tracking.
Every number,
explained.
A Certificate of Analysis is the receipt of the science. Here are the four lines we expect a researcher to check first — and the floors we hold ourselves to.
See real COAs- Purity (HPLC)
Quantifies how much of the sample is actually the target peptide.
≥ 99.0% - Identity (MS)
Mass spectrometry confirms the molecule is what the label claims.
Mass match ± 1 Da - Endotoxin
Bacterial contamination — critical for any reconstituted compound.
< 0.5 EU / mg - Batch ID
Ties every vial back to its own raw test data on file at Afiya Labs.
Unique · Retained 12 mo
What we won't ship.
A short list of rules that govern the catalog. If a batch fails any of these, it stays in quarantine and never reaches a researcher.