HomeCapabilities

Manufacturing Capabilities

From raw ingredient sourcing to last-mile delivery, we operate a fully integrated supplement manufacturing platform — NSF-certified, FDA-registered, and built for brands that demand consistency.

NSF Certified Facility
FDA-Registered Facility
Third-Party Tested

Dosage Forms We Manufacture

Capsules

HPMC & Gelatin

Tablets

Compressed & Coated

Powders

Bulk & Stick Packs

Sachets

Single-serve Formats

Full-Service Manufacturing

Everything under one roof

Managing multiple contract manufacturers creates risk, delays, and quality gaps. We consolidate formulation, production, and packaging into a single accountable partner — with one account manager and one point of contact.

Custom Formulation

Science-backed formulas built for your brand

Our in-house R&D team develops proprietary formulations from scratch or refines existing formulas to meet your efficacy, cost, and regulatory targets. Every ingredient is sourced from qualified vendors and verified for identity, potency, and purity before use.

What's Included

  • Novel ingredient research & selection
  • Bioavailability optimization
  • Stability and compatibility testing
  • Regulatory guidance (FDA, NSF)
  • Nutritional panel & label claim support
  • Prototype development & sensory evaluation

Manufacturing

cGMP-compliant production at scale

Our FDA-registered, NSF-certified facility operates under current Good Manufacturing Practices with full batch traceability. We run dedicated production lines for encapsulation, tableting, and powder filling.

What's Included

  • Hard-shell capsule encapsulation (HPMC & gelatin)
  • Tablet compression & film coating
  • Powder blending & filling
  • Sachet & stick-pack manufacturing

Packaging & Labeling

Retail-ready presentation from concept to shelf

We offer a full range of primary and secondary packaging formats with in-house labeling and artwork review. Our team ensures every package meets FDA labeling requirements and your brand standards before it leaves the facility.

What's Included

  • HDPE & PET bottles (30–500cc)
  • Amber glass bottles
  • Flexible pouches & stand-up bags
  • Blister packs & clamshells
  • Shrink-sleeve & pressure-sensitive labeling
  • Artwork review & compliance check

Quality & Compliance

Third-party verified. Every batch. No exceptions.

Quality is built into every step of our process — not added at the end. We maintain a comprehensive quality management system with SOPs, deviation tracking, CAPA programs, and third-party laboratory testing on every production batch.

What's Included

  • NSF Certified Facility manufacturing
  • FDA-registered facility (21 CFR Part 111)
  • Third-party potency & purity testing
  • Heavy metals, microbial & pesticide panels
  • Certificate of Analysis (COA) for every lot
  • Vendor qualification & raw material testing

How It Works

From concept to customer in 6 steps

Our streamlined process is designed to get your product to market quickly without cutting corners on quality or compliance.

01

Discovery Call

We learn your brand goals, target market, and product vision.

02

Formulation & Quoting

R&D develops your formula; we provide a detailed cost proposal within 5 business days.

03

Artwork & Compliance

Our team reviews label artwork for FDA compliance and brand accuracy.

04

Production

Your batch is manufactured, tested, and documented under cGMP controls.

05

QC Release

Third-party COA issued. Product released only after all specs are met.

06

Shipment Ready

Product packaged, labeled, and prepared for shipment to your warehouse or distribution center.

Quality Assurance

Third-party tested. Every batch. No exceptions.

We don't release a single unit without a Certificate of Analysis from an accredited third-party laboratory. Every batch is tested for identity, potency, heavy metals, microbial contamination, and pesticide residues — and every COA is available to you in the client portal the moment it's issued.

Identity & potency verification
Heavy metals panel (USP 232/233)
Microbial contamination testing
Pesticide residue screening
Allergen cross-contamination controls
Stability & shelf-life studies

NSF Certified

FDA Registered

Facility

100%

Third-party tested

cGMP

21 CFR Part 111

3,000

Minimum Order Quantity

units per SKU

6–10

Average Lead Time

weeks from PO

50+

Dosage Form Variants

across all categories

1 Day

Quote Turnaround

for standard formulas

14 Days

Custom Formula Turnaround

from submission to proposal

Ready to start your project?

Tell us about your product and we'll respond within one business day with a detailed proposal, pricing, and timeline.