PanAmFarma is a Mexico-based pharmaceutical company focused on the sourcing, supply, distribution, manufacturing coordination, and development support of specialized medicines for Latin America.
We support institutional, government, hospital, and authorized B2B pharmaceutical channels with access to difficult-to-source medicines, including biosimilars, oncology products, monoclonal antibodies, vaccines, plasma-related products, selected generics, and other regulated therapies.
Our work is centered on three core areas: regulated access to high-complexity medicines, cross-border pharmaceutical supply coordination, and development support for selected biosimilar, generic, and complex pharmaceutical products.
Our Background
Our historical operating background dates back to 1978, when international pharmaceutical distribution across Latin America depended on handwritten documentation, telex communications, long-distance coordination, and trusted professional relationships.
One of our earliest consignments involved a cold-temperature shipment packed in insulated gel-ice containers and routed from Boston to Mexico City aboard Pan American World Airways, before onward transfer to Bogotá.
What We Do
- Specialty pharmaceutical sourcing and supply coordination.
- B2B distribution to authorized pharmaceutical channels.
- CDMO-linked development and manufacturing support.
- Biosimilar formulation and early regulatory alignment.
- Quality and regulatory documentation support.
- Cold-chain and controlled logistics coordination where required.
Growth and Regional Expansion
Building on its foundation in specialized medicines, PanAmFarma expanded into India-based pharmaceutical manufacturing, developed international collaborations through London-based pharmaceutical channels, acquired Mexican distribution capabilities, and completed a strategic reorganization in 2022 to strengthen its presence across Latin America.
Therapeutic Focus
Our product focus includes monoclonal antibodies, biologics, biosimilar insulins, oncology and chemotherapeutic medicines, vaccines, plasma and blood-derived products, selected generic medicines, and API or formulation materials under applicable controls.
Compliance Approach
Product availability, documentation, registration status, and import requirements are reviewed case by case according to the molecule, destination country, buyer qualification, manufacturer release status, and applicable regulatory pathway.
PanAmFarma works with qualified buyers, manufacturers, logistics partners, and regulatory channels to support compliant pharmaceutical transactions. Documentation, release status, import authorization, commercial terms, and quality requirements are confirmed transaction by transaction.
Professional Notice: PanAmFarma does not provide medical advice. Regulated pharmaceutical products are supplied only under applicable legal, regulatory, quality, and commercial requirements.