Educational positioning

COA (Certificate of Analysis)

Lot-wise analytical testing reports available for each batch.

Overview

A Certificate of Analysis (CoA) summarizes analytical results for a defined batch—identity, potency, contaminants, and microbiology as specified—so buyers can trust release decisions and customs filings.

Typical documentation flow

High-level pathway Fieldston Wellness uses when aligning claims, suppliers, and buyer evidence—not a substitute for legal or regulatory advice for your jurisdiction.

Specification authoring

Define tests, limits, and references per SKU.

Sampling & custody

Link samples to batch IDs and shipment lots.

Laboratory execution

Complete testing under agreed methods.

Controlled release

Distribute CoAs under confidentiality with audit trail.

Frequently asked questions

What belongs on a CoA?

Typically batch identifiers, test methods, results, specifications, and release signatures from an accredited or qualified lab.

Are CoAs country-specific?

Import teams may ask for localization, translations, or alignment with HS codes and invoices for clearance.

How do CoAs relate to specifications?

Specifications set acceptance limits; CoAs prove conformance for that lot—both should reference the same revision.