Manufacturing coordination
Start with as few as 1,000 units. We've vetted every facility in our network for GMP compliance, on-time delivery, and consistent quality.
Most supplement brands don't need their own factory. They need access to the right one. Our manufacturing coordination service connects you with GMP-certified facilities across Canada and the USA that specialize in your specific dosage form and volume requirements.
We've built relationships with 6 manufacturing partners over the years, and we know which facility handles capsules best, which one turns around powder blends fastest, and which can accommodate a 1,000-unit test run without making you feel like a small fish. Every facility in our network undergoes annual audits and maintains current Good Manufacturing Practices (cGMP) certification.
You get a dedicated project manager who coordinates between you and the facility. We handle production scheduling, quality checkpoints, and shipping logistics so you can focus on selling your product.
What's Included
Low MOQ starting at 1,000 units. Ideal for market testing
All facilities are GMP-certified and audited annually
Capsules, tablets, softgels, powders, gummies, liquids, and sachets
Why Brands Choose This Service
Low minimums, real flexibility
Start at 1,000 units to test your market. Scale to 100,000+ when demand picks up. No long-term volume commitments required.
Facility matching
We don't use a one-size-fits-all approach. We match your product to the facility that specializes in your dosage form, ingredient profile, and timeline.
Quality you can verify
Every batch ships with a Certificate of Analysis from an ISO 17025 accredited lab. You see the test results before product leaves the facility.
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Frequently Asked Questions
What is the minimum order quantity for a supplement manufacturing run?
Our network supports MOQs starting at 1,000 units for most common dosage forms. Capsules, tablets, powders, and stick packs. Specialty formats like softgels, gummies, and functional beverages typically start at 3,000 to 5,000 units depending on the facility.
How long does a typical manufacturing run take?
From purchase order to finished, packaged inventory, most straightforward private-label runs ship in 4 to 8 weeks. Custom formulations add formulation and stability time on top, typically pushing the full cycle to 12 to 20 weeks.
Are all your manufacturing partners GMP certified?
Yes. Every facility in our network is cGMP certified under 21 CFR Part 111 in the USA, or operating under Health Canada's Natural Health Products GMP framework with a valid Site Licence in Canada. We don't work with non-compliant facilities.
Can you manufacture both in Canada and the USA?
Yes. We have GMP-certified partners in British Columbia, Ontario, California, Utah, Texas, and Georgia. We match your product to the facility that fits your dosage form, volume, target market, and regulatory requirements.
Do I get a Certificate of Analysis with my finished product?
Every batch ships with a Certificate of Analysis from an ISO 17025-accredited third-party lab covering identity, potency, heavy metals, microbial, and contaminant testing. You review the CoA before the product leaves the facility.
Ready to Get Started?
Tell us about your project and we'll put together a plan and quote tailored to your product, timeline, and budget.