Cannabis manufacturing software with GPP, seed-to-sale + COA in one place — from cultivation batch to child-resistant pack.
Medical and adult-use cannabis manufacturing under Good Production Practices — cultivation batch → extraction → formulation → packaging → COA release → state track-and-trace — with Metrc / BioTrack reconciliation, potency and pesticide result gating, and an evidence base clean enough to convert to EU-GMP when the export door opens.
You're shopping because state track-and-trace, lab COA, and internal batch records live in three systems that don't agree.
Metrc / BioTrack package weights drift from internal batch weights
Potency and pesticide COA arrive by PDF — nobody enforces them as release gates
Cultivation batch → extract lot → formulated lot traceability is a spreadsheet
Child-resistant packaging and label control are manual
Recall from a positive pesticide result takes days, not hours
EU-GMP export path is blocked by the current evidence model
Cannabis, run as one regulated batch flow.
Cultivation → extract → formulation genealogy
Every finished-goods lot traces back through the formulated lot, the extract lot, the biomass batch and the cultivation harvest — one click, not a spreadsheet.
Metrc / BioTrack reconciliation
Package weights, transfers, adjustments and destructions reconciled between the state system and internal batch records — variances flagged before month-end.
Potency + pesticide COA gating
Third-party lab COAs (potency, pesticides, heavy metals, microbials, residual solvents, mycotoxins) ingested and enforced as release gates. No COA, no release.
Good Production Practices
Health Canada GPP (Cannabis Regulations) and comparable state GMP requirements evidenced as live workflow — sanitation, personnel, equipment, quality.
Packaging + label control
Child-resistant packaging spec, THC/CBD label content, warning statements and provincial/state variants version-controlled and lot-linked.
Recall + adverse event
Positive result on any release gate isolates all downstream lots in seconds. Adverse-event log integrates with complaint handling and reporting obligations.
What changes when cannabis manufacturing is one live system.
- Metrc / BioTrack variances drop to near zero at month-end reconciliation
- No lot ships without a passed COA on every required analyte
- Recall isolation from a single positive result is minutes, not days
- Cultivation-to-consumer trace is one query for regulators and insurers
- Same evidence base becomes the foundation for EU-GMP qualification
- State inspection findings on documentation drop toward zero
Every framework a cannabis QA director juggles.
Good Production Practices (Health Canada)
Cannabis Regulations SOR/2018-144 Part 5 — GPP for cannabis products including quality assurance person, standard operating procedures, sanitation program, and record retention.
State GMP / GPP frameworks
State-level GMP or GPP frameworks (e.g. California DCC, Colorado MED, New York OCM) supported through the same underlying evidence engine — configured per jurisdiction.
State seed-to-sale (Metrc / BioTrack)
Bi-directional reconciliation with Metrc, BioTrack and comparable state systems for packages, transfers, adjustments, harvests and destructions.
EU-GMP pathway
For operators exporting to EU medical markets, the same evidence base supports EU-GMP Part II (API-grade) qualification without re-implementing the QMS.
21 CFR Part 11 / Annex 11
Bound e-signatures and hash-chained audit trail for jurisdictions treating records under Part 11 / Annex 11 equivalents.
Cannabis manufacturing software, answered.
What is cannabis manufacturing software?
Cannabis manufacturing software is the QMS + MES + batch-record platform that runs a licensed cannabis producer — cultivation batch, extraction, formulation, packaging, COA release and state track-and-trace — with the evidence base regulators, third-party labs and (for medical exporters) EU-GMP qualification all rely on. It replaces the three-system mess of Metrc + a lab-COA PDF folder + a shared spreadsheet.
Does V5 replace Metrc or BioTrack?
No. State track-and-trace systems are the regulatory system of record — V5 reconciles against them. Package weights, transfers, adjustments and destructions are pushed to and reconciled with Metrc or BioTrack. V5 is the operating system; Metrc is the reporting endpoint.
How are lab COAs enforced?
Third-party lab COAs (potency, pesticides, heavy metals, microbials, residual solvents, mycotoxins) are ingested and mapped to release gates on the lot. A lot without a passed COA on every required analyte cannot be released to packaging or shipped. No PDF-in-a-folder shortcut.
Can V5 handle both medical and adult-use in one facility?
Yes. Product classifications, label requirements, packaging specs and channel-of-trade restrictions are configured per SKU and per destination. Medical and adult-use SKUs coexist without cross-contamination of records.
How does V5 support the EU-GMP export path?
The evidence base — signed batch records, validated equipment, qualified personnel, controlled documents, deviation and CAPA handling, stability — is already structured for GMP inspection. EU-GMP qualification becomes a documentation-overlay project, not a rebuild.
How long does implementation take?
Most cannabis manufacturers reach a GPP + Metrc-reconciled state within 10–14 weeks — cultivation-to-consumer genealogy, COA gating, packaging control, deviation and recall live. Operators pursuing EU-GMP typically add a further 4–6 months of qualification overlay.
Run Metrc, GPP and the lab COA as one release gate.
Free trial. Real seed-to-sale evidence. No sales gate.