Your gateway to 650 million consumers across Latin America.

Most US contract manufacturers ship within the lower 48 and stop there. PMG was built differently. Miami sits at the natural commercial crossroads between North America and Latin America — and our team has spent decades building the regulatory, logistics, and distribution network to move product across that border efficiently and compliantly.

US-based LATAM contract manufacturer.

Brands expanding into Latin America usually face a choice between a US contract manufacturer who cannot support the region and a regional manufacturer who cannot serve the US market. PMG is a US manufacturer built for both: production runs in FDA (Food and Drug Administration)-registered, GMP (Good Manufacturing Practice)-compliant facilities across five US states, while the regulatory and distribution work for Mexico, Brazil, Colombia, Chile, and the Caribbean happens in parallel from our Florida headquarters.

Manufacturing in the United States and exporting from Miami keeps one quality system, one batch record set, and one point of accountability behind both markets. It also preserves the "Made in USA" positioning that carries real weight with LATAM consumers in the beauty, supplement, and wellness categories — without the reformulation that a separate regional manufacturer would require.

The work that makes this practical happens early: ingredient screening against COFEPRIS, ANVISA, and INVIMA restricted lists during formulation, labeling and claim review in the destination language, and registration filings started while US production is still in progress. Project management runs in English and Spanish as a baseline, with working Portuguese for Brazilian engagements.

Why the Miami advantage is real.

Geography

Miami is the closest major US metro to both Mexico and South America, with the highest density of LATAM trade infrastructure, logistics providers, and import/export expertise in North America.

Regulatory depth

Decades of team experience working with COFEPRIS (Mexico), ANVISA (Brazil), INVIMA (Colombia), and regulatory bodies across the region. We build LATAM registration into your product spec from day one.

Language and culture

Bilingual project management as a baseline, not a premium. Operational fluency in English, Spanish, and working knowledge of Portuguese — because regulatory submissions in Mexico and Brazil are done in the local language.

The markets we know.

🇲🇽

Mexico

·COFEPRIS regulatory pathway
·2–6 month registration
·Largest LATAM opportunity for most US brands

🇧🇷

Brazil

·ANVISA regulatory pathway
·12–18 month registration
·Portuguese-language submissions
·Largest LATAM market by GDP

🇨🇴

Colombia

·INVIMA regulatory pathway
·Rapidly growing middle class
·Strategic gateway to Andean region

🇵🇪

Peru / Chile / Argentina

·DIGEMID, ISP, ANMAT pathways
·Andean market cluster

🌎

Caribbean

·Puerto Rico (US regulatory — no extra registration needed)
·Dominican Republic, Jamaica
·Shorter regulatory pathways
·Proximity logistics advantage

LATAM readiness built in from day one, not bolted on.

Most brands discover the cost of LATAM expansion too late — after a successful US launch, when reformulating and re-registering a product for international markets is expensive and time-consuming. PMG eliminates that cost by building cross-border compliance into your product from the start.

Day 1 formulation

Ingredient lists reviewed against COFEPRIS, ANVISA, and EU restricted ingredient standards simultaneously. LATAM-compliant from the first batch.

Registration in parallel

While your US launch is in production, our regulatory team begins the registration filings in your target LATAM markets. The launches overlap rather than sequence.

LATAM channel activation

Established distributor relationships in Mexico, Colombia, and key Caribbean markets. We introduce your product to the right buyers.