International brands entering North America
Cross-border supplement launches die in the paperwork. Whether you're a brand entering the US and Canadian market or you want Made-in-USA/Canada product to sell abroad, the regulatory layer (NPNs, FDA requirements, bilingual labels, export documentation) is where most international launches stall. We've handled launches in both directions. We manufacture in GMP-certified US and Canadian facilities, manage the registrations, and prepare the export paperwork, so a brand that doesn't know North American rules can still launch here cleanly.
The roadblocks we take off your plate
North American supplement regulations look nothing like the rules in your home market.
We translate your products into what FDA and Health Canada require, including NPN applications and the right label format for each country.
You need product labeled and registered for Canada, which means French and English.
We produce compliant bilingual labels and handle the NPN process, so your product is legal to sell from day one.
You want a Made-in-USA or Made-in-Canada product for your own market, but coordinating that from abroad is hard.
We manufacture in GMP-certified North American facilities and prepare the export documentation your destination market needs.
Managing manufacturers, labs, and regulators across a time-zone gap is a nightmare.
One point of contact in North America manages all of it on your behalf, so you're not chasing vendors at 3 a.m.
What you get working with us
- Enter the US and Canadian market without learning two regulatory systems yourself
- Get compliant bilingual labels and NPN registration handled for Canada
- Manufacture in GMP-certified US or Canadian facilities, with Made-in-North-America on the label
- Prepare export documentation for selling North American-made product abroad
- Work through one North American contact instead of coordinating vendors across time zones
Services that fit this stage
Frequently asked questions
Yes. For Canada we apply for the NPNs your products need; for the US we make sure the product and facility meet FDA requirements. You don't need a North American entity to manufacture with us, though selling locally may have its own importer or business requirements we'll flag.
For Canada, yes. Labels have to be bilingual, English and French, and we produce compliant bilingual labels as part of the process. US labels are English-only but follow different FDA formatting rules, which we also handle.
Yes. We manufacture in GMP-certified US and Canadian facilities and prepare the export documentation for your destination market. The in-country product registration on the other end usually sits with the importer or a local agent, and we'll tell you where that line is.
You get one point of contact who manages the manufacturers, labs, and regulators here. You make decisions on your schedule; we run the day-to-day coordination on North American business hours.
Ready to take the launch off your plate?
Tell us where you are and we'll put together a plan, a timeline, and an honest quote tailored to your product and budget.