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 SCIENCES

Research & Development

Formulation scientists in our US lab, specializing in oral delivery systems, active stability, and flavor engineering. Every R&D cycle runs three parallel tracks: active optimization, mouthfeel calibration, and shelf-life projection. 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+ in-house profiles
02
IN-HOUSE TESTING

Analytical chemistry

Every batch goes through analytical review before product ships. Testing methods, documentation, and retention samples follow industry standards and cGMP requirements. Your release paperwork is ready when retail or regulatory asks.

BATCH RELEASE TESTING
Every production run
POTENCY VERIFICATION
Pre-release, every batch
RETENTION SAMPLES
Held per cGMP
DOCUMENTATION
Audit-ready
03
MOIST / SEMI-MOIST / DRY

Formulation

Three moisture profiles in production: moist, semi-moist, and dry. Each suits different actives, release curves, and positioning. We formulate to the moisture profile your product needs, not what's easiest to run.

ACTIVE DOSE RANGE
0.5mg–300mg
POUCH FORMATS
Standard sizes with custom available
RELEASE PROFILES
Fast, sustained, layered
SWEETENER SYSTEMS
Sized to your positioning
04
DOCUMENTED PRODUCTION

Manufacturing

cGMP-compliant manufacturing in the US, built around documentation discipline. Every production line is cleaned, validated, and recorded between runs. Batch records, COAs, retention samples, and monitoring data ready on request for diligence, audit, and retail buyer review.

PRODUCTION CAPACITY
Multi-million can monthly capacity
CERTIFICATIONS
GMP certified (CGA). NSF and SQF in progress
BATCH SIZE RANGE
10k to 2M cans
05
Design Coordination

Packaging

Design specialists with CPG and pouch experience, coordinated through our curated network. Can design, label systems, secondary packaging, and retail merchandising. Every label reviewed by our in-house QA before print. Already have a creative team? We work with them too.

CAN SIZES
15, 20, 25-pouch standards
LABEL FINISH OPTIONS
Matte, gloss, soft-touch, foil
PRINT MINIMUM
Scaled to run size
DESIGN TURNAROUND
~5 business days
06
REGULATORY REVIEW

Compliance

Every formulation, claim, and label clears in-house regulatory review before it reaches a production line. QA leadership covers FDA dietary supplement product requirements, with quality control supporting production-floor compliance. State-level requirements addressed as they arise for your specific brand and markets.

FDA REGISTRATIONS
Supplement products
LABEL & CLAIMS REVIEW
In-house QA, every formulation
STATE COMPLIANCE
Handled per brand and market
INTERNATIONAL
Supported via EU sister entity
07
FULFILLMENT

Logistics

Manufacturing-to-channel fulfillment built around your brand's sales mix. DTC platforms, Amazon FBA, TikTok Shop, retail broker channels. End-to-end lot traceability. International availability when needed.

DTC FULFILLMENT
Shopify, Amazon FBA, TikTok Shop
RETAIL CHANNELS
McLane, Crossmark
LOT TRACEABILITY
End-to-end
REORDER LEAD TIME
2–3 weeks* (with notice)
CERTIFICATIONS & REGISTRATIONS

Documentation that holds up to audit.

GMP Certified
Certified by Carat Global Assurance (CGA) to the CGA GMP Standard for Dietary Supplements
FDA Registered
Registered with the U.S. Food and Drug Administration
NSF: In Progress
NSF International certification audit in progress
SQF: In Progress
Safe Quality Food certification audit in progress
Non-GMO Verified
Non-GMO Project verified ingredients and processes

Let's make something.

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

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