— Tools / 01

Verify the vial
in your actual hand.

Type the batch number from your vial label or COA card. We'll surface the original certificate, signed by an independent ISO-17025 lab — not us, not our supplier.

Don't have your batch number? It's printed on the kit insert.

Try a recent batch
— How verification works

From synth to your shelf.

Every Element MD batch passes four sequential checkpoints. Any fail at any stage and the batch is destroyed — never reworked, never blended into another lot.

Step 01 · Day 0

Solid-phase synthesis

Built one amino acid at a time at our Tampa facility under cGMP-aligned protocol. Synthesis log entered as the batch ID.

Internal · log signed
Step 02 · Day 4–6

HPLC purity assay

Aliquot pulled and shipped to Janoshik Analytical. High-performance liquid chromatography establishes molecular purity to four decimals.

3rd party · ISO 17025
Step 03 · Day 6–8

Mass spectrometry

The same lab runs MS to confirm molecular weight against the theoretical target. Any deviation > 0.5 Da fails the batch.

3rd party · ISO 17025
Step 04 · Day 9

Endotoxin + sterility

LAL endotoxin assay and sterility culture. Only after all four pass is the batch released. COA is dated and stamped before any vial ships.

3rd party · final release
— Independent partner labs

Every certificate is signed
by a chemist
we don't pay a salary.

Janoshik Analytical
HPLC · MS · Czechia
KP Labs
Endotoxin · sterility · USA
Avg. turnaround
9 days · synth → release
0.0% blended lots
Failed batches destroyed