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Kwaliteit & Naleving

Lab results, by lot

Every lot is tested by a third-party lab and documented with its own certificate of analysis. Look up a lot, or browse the library below.

Bona Voluntate lot seal

Enter a lot number. A rep sends its COA within one business day.

Testen door derden

Three labs, named on every report

The lab that tested a lot is printed on its COA and coded in its file name.

FILE CODE: BDGR
Das

The scope of testing is listed on each report.

FILE CODE: KCA
KCA

The scope of testing is listed on each report.

FILE CODE: ANRS
Anresco

The scope of testing is listed on each report.

COA library

Analysecertificaten

Filter by ingredient and request the latest report. Each report is a PDF named by lab, cannabinoid, form and test date.

File name convention
BDGR
laboratorium
CBD
cannabinoïde
ISO
formulier
07 28 26
date, MM DD YY
Showing 6 of 6 ingredients
LOT
PRODUCT
LAB
DATUM
ZUIVERHEID
VERSLAG
Laatste partij
CBD-isolaat
Named on report
Actueel
Volgens COA
Laatste partij
CBG-isolaat
Named on report
Actueel
Volgens COA
Laatste partij
CBN-isolaat
Named on report
Actueel
Volgens COA
Laatste partij
CBC
Named on report
Actueel
Volgens COA
Laatste partij
CBT
Named on report
Actueel
Volgens COA
Laatste partij
Full and broad spectrum distillates
Named on report
Actueel
Volgens COA

Reports are sent to verified business accounts, usually within one business day.

strekking

What we test and why

Five test categories appear on our reports. The panel for each lot is listed on its COA. Panels vary by product.

01

Sterkte

The amount of each cannabinoid in the lot.

02

Residuele oplosmiddelen

Solvents left over from processing.

03

Zware metalen

Trace metals measured against the report’s limits.

04

Pesticiden

A screen for pesticide residues.

05

microbiële

A count of bacteria, yeast and mold.

Documentatie

Documents on request

Sent to verified business accounts, usually within one business day.

No documents selected.

Veiligheidsinformatiebladen
One sheet per ingredient, for your receiving and compliance files.
GMP quality manual excerpt
Handling and documentation practices, aligned with 21 CFR Part 111.
Customs paperwork package
Commercial documents and lot references for cross-border shipments.
Specificatiebladen
Form, packaging and specification ranges by ingredient.

Need a report we have not listed?

Tell us the ingredient and lot. We respond within one business day.

Vraag naar prijsopgaven en COA's.
Note

A COA describes the tested lot only. Results vary by lot, and a test list is not a promise about any future lot. Products are ingredients for further manufacturing and are sold to verified businesses only. Buyers are responsible for compliance with all laws that apply to their finished products.

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