COA & lab certificate for each batch
Purity >99% · HPLC-tested
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Expert advice for medical practices, doctors, and end customers
Quality & Laboratory Testing

Don't trust it.
Check it out.

Quality is valuable only if it is documented in a traceable manner. That is why we rely on batch-specific tracking and independent HPLC analyses.

The Process

From the sample to a verifiable result.

01

Assign Batch

Each tested sample is assigned to a specific product batch. This provides the basis for traceable documentation.

02

Perform HPLC analysis

The chromatographic analysis assesses the purity of the submitted sample by an independent laboratory.

03

Document the result

The test method, sample, and test results are compiled in the analysis certificate.

04

Provide transparently

Available quality information is clearly communicated on the product or batch.

Read the COA

What is included in a certificate of analysis?

A Certificate of Analysis—or COA for short—summarizes the key findings of a laboratory test. What matters is not just a percentage, but the relationship between the sample, the method, the date, and the result.

Sample NameWhich sample was analyzed?
Test MethodHow were the measurements taken?
ResultWhat purity was determined?
Date / ReferenceWhen and under which ID?
Important to understand

What HPLC Tells Us—and What It Doesn't.

HPLC purity

HPLC describes the relative proportion of the main component detected in the sample being analyzed.

No Guarantee of Effectiveness

A purity rating does not indicate any medical effect, suitability, or safety of use.

Batch-based ordering counts

A certificate is particularly meaningful when the sample and the batch being offered are clearly linked.

Do you have questions about a quality document?

We'll help you figure it out and explain where to find the relevant information.

FOR RESEARCH PURPOSES ONLY · NOT INTENDED FOR USE ON OR IN THE HUMAN BODY