The infrastructure
behind every pouch.
Seven operational disciplines. Every one in-house. Every one documented. This is the technical stack that lets us ship a category-defining product in 4–6 weeks — and back it with the data to prove it holds up.
Research & Development
Formulation scientists across our US and UK labs, specializing in oral delivery systems, active stability, and novel flavor engineering. Every R&D cycle runs three parallel tracks — active optimization, mouthfeel calibration, and shelf-life projection — so you hit market with a product that holds up.
- Lab scale batching
- 500g — 10kg
- Typical R&D cycle
- 2 weeks
- Active ingredient library
- 180+ validated inputs
- Flavor system library
- 40+ proprietary profiles
Analytical chemistry
HPLC, GC-MS, and dissolution testing performed in-house on every batch. We don't wait on third-party labs for release testing — which is why our production windows are tight and our consistency data is rigorous enough to support PMTA and NDI submissions.
- HPLC systems
- Agilent 1260 series
- Potency test turnaround
- 4 hours
- Retention sample policy
- 2 years per batch
- Stability chambers
- ICH Q1A compliant
Formulation
All three pouch moisture profiles in production. Semi-moist (20–35% water) is our default modern platform — Zyn-category firmness, 12+ month shelf stability at room temperature. Moist for traditional positioning. Dry for heat-sensitive actives and extended-release curves.
- Active dose range
- 0.5mg — 500mg
- Pouch formats
- Slim, regular, extra-strong
- Release profiles
- Fast, sustained, layered
- Sweetener systems
- Sugar, stevia, monk fruit, erythritol
Manufacturing
cGMP-compliant facilities across the US, UK, and continental Europe. Every production line is cleaned, validated, and documented between runs. Dedicated lines for regulated categories. Full batch records with retention samples, analytical COAs, and environmental monitoring data delivered with every shipment.
- Production capacity
- 5M+ cans / month
- Certifications
- cGMP, ISO 9001, ISO 22000
- Line separation
- Nicotine and functional isolated
- Batch size range
- 50k — 2M cans
Packaging
Four staff designers with CPG backgrounds. Can design, label systems, secondary packaging, and retail merchandising. Every label reviewed by regulatory before print. We also work seamlessly with your existing creative team if you prefer to own the design.
- Can sizes
- 15, 20, 25-pouch standards
- Label finish options
- Matte, gloss, soft-touch, foil
- Print minimum
- 25,000 cans
- Design turnaround
- 5 business days
Compliance
Specialists on staff covering FDA (dietary supplement, food, tobacco), PMTA and MRTP submissions, EU TPD, UK equivalents, and state-level requirements for regulated categories. Every formulation, claim, and label clears regulatory review before it reaches a production line.
- FDA registrations
- Food, supplement, tobacco
- PMTA manufacturing docs
- Supported end-to-end
- State compliance tracking
- All 50 states maintained
- International
- EU TPD, UK MHRA, Canada NNHPD
Logistics
Integrated 3PL partnerships across North America, the UK, and continental Europe. Direct DTC fulfillment, retail distribution, reorder automation, and customs-cleared international shipping. Lot traceability end-to-end so a recall stays surgical if it ever needs to be.
- DTC integrations
- Shopify, Amazon FBA, Faire
- Retail distribution
- US C-store, specialty, natural
- International shipping
- 50+ countries
- Lead time on reorder
- 2–3 weeks
Documentation that holds up to audit.
Let's make something.
A 30-minute call with our team tells you more than any RFP.