Quality & Lab Testing
Transparency
Quality & Lab Testing
Every batch of Celvity NMN is individually tested to verify potency and safety. NMN content is confirmed by HPLC, and heavy metals — lead, arsenic, cadmium, and mercury — are verified within EU limits (Commission Regulation (EC) 1881/2006). Each certificate below corresponds to the lot number printed on your bottle.
Current batches — Lot 20264 & Lot 20263: NMN content confirmed by HPLC · heavy metals within EU limits (Commission Regulation (EC) 1881/2006) · independently tested.
The NMN raw material used in these batches is verified at 99.93% purity by 1H-NMR — see the raw-material certificate below.
Certificates of Analysis
Finished-product test reports for the current batches.
| Batch (Lot) | Product | Certificate |
|---|---|---|
| Lot 20264 Current | NMN — 30 Capsules | View PDF |
| Lot 20263 Current | NMN — 30 Capsules | View PDF |
Raw material
Incoming NMN raw-material analysis from our manufacturer — 99.93% purity (1H-NMR).
| Material | Certificate |
|---|---|
| β-Nicotinamide Mononucleotide (NMN) | View PDF |
Manufacturing certifications
Our manufacturing partners are independently audited to internationally recognized food-safety and quality standards.
| Standard | Scope | Certificate |
|---|---|---|
| FSSC 22000 | Food Safety System Certification — supplement production (CureSupport, Netherlands) | View PDF |
| ISO 22000:2018 | Food-safety management — food-supplement manufacturing & packing (Contract Pharma Solutions, Lithuania) | View PDF |
| GMP — FDA 21 CFR Part 111 | Audited to FDA cGMP for dietary supplements (21 CFR Part 111) | View PDF |
| ISO 13485:2016 | Manufacturing partner's medical-device quality management system (Contract Pharma Solutions) — reflects overall manufacturing quality capability, not a device claim for this product | View PDF |
ISO 13485 is a medical-device quality standard held by our manufacturing partner and is shown here as evidence of their quality systems; Celvity NMN is a food supplement, not a medical device.