For manufacturers
Reach Latin America with a partner who knows the regulatory path and the people on the ground. We find and qualify distributors, check what registration will require, and help structure the agreement.
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ROW Consulting sources products, qualifies partners and structures agreements, backed by more than 20 years in global regulatory affairs.
Reach Latin America with a partner who knows the regulatory path and the people on the ground. We find and qualify distributors, check what registration will require, and help structure the agreement.
Learn more →Find medical devices and drug products that fit your portfolio. We source, qualify the manufacturer, and help you agree on terms before you commit.
Learn more →Finding and qualifying suppliers for medical devices and drug products.
Identifying distributors, opening doors and structuring commercial agreements.
Strategy, registration guidance and lifecycle support, offered on a limited basis.
We start with a call about what you make, or what you need to find.
We map the market, the partners and the regulatory requirements.
We check each potential partner before any introduction.
We help both sides reach terms that work, then stay involved through launch.

Our founder has worked in regulatory affairs for more than 20 years, including WHO prequalification of drug products.
We have built an LTR network in Latin America and work with national regulatory authorities in five global regions.
You work directly with the person who runs the engagement.
Regulatory affairs consulting is offered on a limited basis. Contact us to discuss availability.
Review regulatory services →A short conversation is usually enough to know if we can help.