Capabilities

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.

01
In-house scientists

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
02
In-house testing

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
03
Moist, semi-moist, dry

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
04
Pharma-grade production

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
05
Design studio in-house

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
06
Regulatory team

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
07
Global fulfillment

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
Certifications & registrations

Documentation that holds up to audit.

cGMP
Current Good Manufacturing Practice
ISO 9001
Quality management
ISO 22000
Food safety
FDA
Food, supplement, tobacco registered
PMTA-ready
Documentation supports filing
EU TPD
Tobacco Products Directive
Non-GMO
Capable on request
Organic
Certified line available
Your brand. Your way.

Let's make something.

A 30-minute call with our team tells you more than any RFP.