Low MOQ from 3,000 bottles • FDA-registered facility • cGMP quality system • In-house testing
Built for Clean Labels: Encapsulate With or Without Magnesium Stearate
Many brands want to eliminate magnesium stearate to support clean-label positioning and meet consumer expectations. Atrium can run formulas with or without magnesium stearate depending on your ingredient profile, capsule size, and performance requirements.
How we support mag-stearate-free programs:
- Flow and fill optimization
- Alternative flow strategies
- Pilot validation at low MOQ before scaling to high-speed output
- Transparent formulation tradeoffs (cost, throughput, and feasibility)
If you want the cleanest label possible, we’ll help you design a manufacturing-ready powder system that fills consistently—without relying on magnesium stearate.
High-Speed Capsule Manufacturing Capacity (Designed to Scale)
Atrium’s capsule manufacturing line is built for brands that need speed-to-market now and scalability later.
Ribbon Blender – Uniform Powder Blending
Capability Table
| Capability | Atrium Specification | Notes |
|---|---|---|
| Encapsulation / Packaging Output | Up to 110,000 capsules/hour | Depends on capsule size, fill weight, powder flow, and packaging configuration* |
| Powder Blending | 2 blenders up to 750 kg per batch | Capacity varies by powder density and blend profile* |
| Minimum Order Quantity | From 3,000 bottles | Bottle count depends on count-per-bottle and capsule size* |
| Manufacturing Location | Made in USA (California) | Supports reshoring and domestic supply goals |
*Estimated/variable by project. Final specs confirmed during feasibility and pilot.
cGMP Quality System + FDA Registration
Atrium operates with a quality system aligned to dietary supplement cGMP requirements and maintains appropriate FDA facility registration for dietary supplement operations. Dietary supplement manufacturers, packagers, and labelers are subject to 21 CFR Part 111 cGMP requirements.
FDA food facility registration requirements are addressed under 21 CFR Part 1, Subpart H, with FDA systems supporting facility registration submissions.
Quality system highlights:
Master manufacturing records + controlled batch documentation
Ingredient receiving controls and traceability (lot-to-lot visibility)
In-process checks for weight, appearance, and process conformity
Controlled release workflow with documented disposition decisions
Deviation/CAPA practices designed for repeatable outcomes
If you have a specific customer audit checklist, we’ll align documentation packages accordingly (as applicable to your program
In-House Testing to Move Faster & Reduce Outsourcing Delays
Atrium’s internal testing capability supports faster development cycles, tighter process control, and smoother scale-up—especially for brands running multiple SKUs or frequent production cycles.
Atrium’s in-house testing lab supports quality control and finished product specifications for Made-in-USA contract manufacturing.
Common testing support areas (example list):
Incoming material screening (project-appropriate checks)
In-process verification to prevent rework
Finished product release support (as defined in your quality agreement)
Stability planning support for shelf-life confidence (when requested)
For tests requiring independent ISO/IEC 17025 scope, we can coordinate qualified third-party labs while maintaining chain-of-custody controls.
In-process verification to prevent rework
Finished product release support (as defined in your quality agreement)
Stability planning support for shelf-life confidence (when requested)
For tests requiring independent ISO/IEC 17025 scope, we can coordinate qualified third-party labs while maintaining chain-of-custody controls.
What We Manufacture
High-Speed Capsule Filling Machine (Up to 75,000 Capsules/Hour) | Atrium Scientific
Atrium supports powdered capsule programs across many supplement categories, including:
Vitamins and micronutrient blends
Botanical and functional powders (where feasible)
Amino acid and nootropic-style blends (flow-dependent)
Multi-ingredient “stack” formulas (pilot validated before scale)
Capsule options:
Standard capsule sizes and counts-per-bottle targets
Clean-label excipient strategies (including mag-stearate-free programs)
Vegan or Non-Vegan capsules
Atrium supports powdered capsule programs across many supplement categories, including:
Vitamins and micronutrient blends
Botanical and functional powders (where feasible)
Amino acid and nootropic-style blends (flow-dependent)
Multi-ingredient “stack” formulas (pilot validated before scale)
Capsule options:
Standard capsule sizes and counts-per-bottle targets
Clean-label excipient strategies (including mag-stearate-free programs)
Vegan or Non-Vegan capsules
Low MOQ From 3,000 Bottles
Low MOQ Capsule Manufacturing Services (USA cGMP) | Atrium Scientific
Not every brand wants (or needs) a massive first run. Atrium’s low MOQ starting at 3,000 bottles is built for:
New SKU launches by established brands
Market tests and channel expansion
Reformulations and “clean label” upgrades
Line extensions and seasonal releases
Why we offer low minimum order quanity:
Validate demand without overbuying inventory
Reduce cash tied up in first production lots
Iterate faster with real market feedback
Scale into higher throughput once the product proves itself
Not every brand wants (or needs) a massive first run. Atrium’s low MOQ starting at 3,000 bottles is built for:
New SKU launches by established brands
Market tests and channel expansion
Reformulations and “clean label” upgrades
Line extensions and seasonal releases
Why we offer low minimum order quanity:
Validate demand without overbuying inventory
Reduce cash tied up in first production lots
Iterate faster with real market feedback
Scale into higher throughput once the product proves itself
Our Manufacturing Process: Simple, Transparent, Repeatable
In-house testing that supports cGMP quality systems and verification of finished product specifications.
1) Feasibility & quote
We review your formula, capsule targets, label claims direction (non-medical), and packaging configuration.
1) Feasibility & quote
We review your formula, capsule targets, label claims direction (non-medical), and packaging configuration.
2) Pilot run (low MOQ)
We confirm blend behavior, encapsulation consistency, and packaging workflow.
3) Scale-up planning
We optimize throughput and cost targets while maintaining quality controls.
4) Production + QC release
Documented manufacturing with defined checks and release steps.
We confirm blend behavior, encapsulation consistency, and packaging workflow.
3) Scale-up planning
We optimize throughput and cost targets while maintaining quality controls.
4) Production + QC release
Documented manufacturing with defined checks and release steps.