cGMP Certified· NSF / ANSI 455-2
FDA Registered· Reg. #3014285621
ISO 17025· Accredited Lab
Form 483· Zero Observations — 2025

200,000 sq ft · cGMP Certified Facility

Your Formula.
Engineered to the microgram.

Contract supplement manufacturing for DTC founders, clean-label reformulators, and retail-ready brands. One partner. Every stage.

Enteric CoatingIndia · 99.2% purityActive BlendMulti-origin · COA on fileFlow AgentUSA · 98.8% purityVegetal Cellulose ShellGermany · 99.7% purityMoisture BarrierJapan · 99.9% purity
200K
Square Feet
cGMP Facility
100K+
Unit Minimum
Custom Formulas
21 CFR
Part 111
Compliant
48hr
Sample Turnaround
Qualified Lots
Pharmaceutical scientist in white lab coat and blue nitrile gloves weighing botanical raw materials on a precision analytical balance inside a clean room

01Formulation

Custom formulas built from the molecular level up.

From DSHEA-compliant botanical extracts to precision amino acid matrices and mineral chelates — our formulation team works in microgram tolerances. Raw materials are quarantined, identity-tested, and released by our in-house QC team before a single gram enters the blend.

2,400+
Active Formulas on File
30-day
Avg. Formulation Cycle
50+
Ingredient Categories
N₂ Blended
Nitrogen-Purged Process
cGMP Cert

NSF/ANSI 455-2 · Third-party audited annually

View Certificate ↗
DSHEA

21 CFR Part 111 · Full compliance documentation

View Reg. Filing ↗

02Sourcing & Ingredient Integrity

We test every lot. Every time.

Supplier COAs are the floor, not the ceiling. Every incoming raw material is quarantined and independently tested for identity, potency, microbiological compliance, and heavy metal burden before release. HPLC identity testing and DNA barcoding prevent adulteration at the source.

100%
Incoming Lot Testing
GMP-Cert
Approved Supplier Program
DNA
Barcoded Identity Test
Full
Traceability Reports
COA

Certificate of Analysis issued per lot · Available on request

Sample COA ↗
Kosher / Halal

Dual-certified production runs available

View Certs ↗
Close-up of rows of amber glass jars containing raw botanical ingredient powders lined up on stainless steel shelving inside a pharmaceutical warehouse
Industrial pharmaceutical blending equipment with stainless steel drums and powder mixing chambers in a temperature-controlled clean room manufacturing facility

03Blending & Encapsulation

Homogeneous to the last microgram.

Dry blending under nitrogen atmosphere. Tablet compression to ±2% weight variance. Microencapsulation for sensitive actives, flavor masking, and controlled-release profiles. Every blend validated by in-process checks before encapsulation or compression begins.

±2%
Tablet Weight Variance
N₂
Nitrogen Atmosphere Blend
00–4
Capsule Size Range
Micro
Encapsulation Available
Non-GMO

Available on qualifying formulas

View Verification ↗
FSSC 22000

Food Safety System Certification · Audit 2025

View Certificate ↗

05Packaging & Scale

From 100K units to 10 million.

Automated filling lines for bottles, jars, and blister packs. Real-time barcode tracking through every stage. Retail-ready labeling with FDA-compliant Supplement Facts Panels, allergen declarations, and channel-specific documentation for Amazon, Walmart, TikTok Shop, and international export.

100K
Capsule Minimum (Custom)
10M+
Unit Monthly Capacity
48hr
Retail Doc Turnaround
GS1
Barcode & Serialization
Amazon Ready

ASIN documentation · FBA compliance packs

Channel Docs ↗
Informed Sport

Certified for Sport testing pathway available

Learn More ↗
Automated pharmaceutical packaging line with conveyor belt moving white supplement bottles through a filling and capping station in a large industrial facility

04 — Analytical Testing

Every batch is verified,
not assumed.

In-house ISO 17025-accredited laboratory. Five analytical methodologies run on every production lot. COA issued before a single unit ships.

HPLC
High-Performance Liquid Chromatography
Potency verification · Active ingredient quantification · Label claim confirmation
USP <621>
ICP-MS
Inductively Coupled Plasma Mass Spectrometry
Heavy metal screening · Pb, As, Hg, Cd · ppb-level detection
USP <233>
FT-IR
Fourier Transform Infrared Spectroscopy
Raw material identity · Adulteration detection · Structural confirmation
USP <854>
Micro Panel
Microbiological Compliance Screen
Salmonella · E. coli · Total aerobic count · Mold & yeast
USP <2021>
UV-VIS
Ultraviolet-Visible Spectroscopy
Concentration assays · Purity screening · Colorimetric analysis
USP <857>
Laboratory scientist operating analytical testing equipment in a pharmaceutical-grade clean room with white walls and stainless steel instruments

Ready to Manufacture

From formula
to retail shelf.
One partner.

DTC founders, established brands, and first-time Amazon sellers — we handle the manufacturing, testing, and documentation so you can focus on the market.

Third-Party Verified
NSF cGMP Certified · #C0076498
FDA Registered · Reg. #3014285621
ISO 17025 · Accredited Testing Lab
Form 483 · Zero Observations, 2025
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