What is a Certificate of Analysis (COA)?
What is a Certificate of Analysis (COA)?
A Certificate of Analysis (COA) is an official lab report that verifies the contents, potency, and safety of general raw materials or cannabis products. It is issued by a licensed third-party laboratory after testing and typically includes:
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Potency Results – THC, CBD, and other cannabinoids
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Terpene Profile – flavor and aroma compounds
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Contaminant Screening – pesticides, heavy metals, mold, microbials
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Residual Solvents (for extracts and concentrates)
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Lot / Batch Identification – links the lab results to specific production batches
Purpose:
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Ensures compliance with state regulatory bodies (e.g., METRC integration in CO, MO, etc.)
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Provides transparency and safety assurance to consumers and buyers
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Serves as a chain of custody document, proving that products meet legal and quality standards
Where is the COA stored in Figgro?
In the Figgro ERP (Seed-to-Sale) system, COAs are treated as compliance and quality documents tied to inventory and product records. Typically, COAs are:
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Uploaded into the Quality & Compliance Module
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Stored against specific lots, batches, or production runs.
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Accessible when creating manifests or sales orders.
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Linked at the Product / Package Level
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Each finished good, bulk ingredient, or raw material has an associated COA.
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If a product is transferred, the COA automatically follows the manifest.
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Attached to Sales & Distribution Documents
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Buyers ( distributors, manufacturers) can download/view COAs directly from Figgro.
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Helps streamline audits and customer trust.
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Archived in the Document Repository
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COAs remain in secure cloud storage for audit trails, with version history and expiration dates and can be found under the Chain of Custody Module---> Manage Lab Reports sub module.
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Ensures alignment with GMP/HACCP compliance by maintaining chain-of-custody traceability.
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In short: A COA in Figgro lives in the Inventory / Compliance layer, directly tied to batches and packages. This ensures it is always available for regulators, internal QA teams, and buyers during manifests, transfers, or audits.