What Is a NY Cannabis Processor?
A processor manufactures finished cannabis products from raw plant material supplied by licensed cultivators.
You operate inside the supply chain, not at retail.
What You’re Allowed to Do
With a processor license, you may:
- Receive raw cannabis from licensed cultivators
- Extract cannabinoids using approved methods
- Manufacture edibles, vapes, tinctures, concentrates, and other approved formats
- Infuse products using compliant ingredients
- Package and label finished products
- Transfer only to licensed distributors or microbusinesses
Processors do not sell directly to consumers or retailers.
What Products Can a Processor Make?
Only product categories approved by OCM, including:
- Edibles (gummies, mints, lozenges)
- Beverages
- Vape cartridges meeting additive rules
- Tinctures and sublingual products
- Topicals
- Concentrates
- Tablets or capsules
Every product must meet potency, formulation, and additive limits.
What You Cannot Manufacture
Processors may not produce:
- Products appealing to children
- Products with prohibited inhalable additives
- High-dose edible formats exceeding legal limits
- Any product that has not passed required laboratory testing
If it fails testing, it does not enter the market.
Facility Requirements
Processors must operate from an OCM-approved facility.
Core requirements include:
- Designated extraction and infusion areas
- Food-grade preparation areas for edibles
- Proper solvent handling (if applicable)
- Secure, locked storage
- Ventilation and fire safety compliance
- Worker protection protocols
- Written Standard Operating Procedures (SOPs)
Your buildout must match your approved application.
Changes require approval.
Packaging and Labeling Rules
Before transfer, products must be:
- Child-resistant
- Tamper-evident
- Opaque (when required)
- Resealable for multi-serving formats
Labels must include:
- THC and CBD per serving and per package
- Full ingredient list
- Processor license number
- Batch or lot number
- Test date
- Universal THC symbol
- Required warnings and disclosures
Unlabeled product cannot move.
Testing and METRC Requirements
Processors must maintain full traceability.
You must:
- Log all incoming material in METRC
- Track batch creation and formulation
- Submit samples for third-party laboratory testing
- Retain Certificates of Analysis (COAs)
- Record destruction of failed product
- Retain records for required periods
Every batch must pass state-required testing before distribution.
If it is not logged, it did not happen.
What Happens If a Batch Fails Testing?
You must:
- Log the failed result
- Quarantine the product
- Follow remediation or destruction protocols
- Document every step
Moving failed product is a serious violation.
What Operators Usually Miss
- You cannot transfer unfinished product
- Facility modifications require approval
- Inhalable additive rules are strict
- Failed lab results must be logged immediately
- Documentation gaps are violations
- Packaging errors can trigger recalls
Processors carry risk across the entire supply chain.
When This Comes Up
- Building out your manufacturing facility
- Adding new product types
- Changing formulations
- Preparing for inspection
- Launching new SKUs
- Responding to failed lab tests
What Happens If You Ignore This
Noncompliance may result in:
- Product quarantine
- Mandatory recalls
- Fines
- Suspension
- License revocation
Manufacturing errors ripple across distributors and retailers.
Processors are held to high scrutiny because product safety affects the entire market.
Related OCM Licensing Section Pages
Source Material