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Rebexa Group is your premier Regulatory Affairs management partner for medical products in Latin America, specifically Central America, the Andean Region, and the Caribbean.

Rebexa Group helps you achieve better control over your company’s product registration and regulatory affairs responsibilities in Central American, Andean Region, and Caribbean markets.

We provide the expertise to help you comply with individual country regulations and registration procedures. Currently, we manage a portfolio of over 2,500 registrations throughout the region in different therapeutic areas such as medical devices, human and veterinary pharmaceuticals.

Rebexa Group offers services tailored to fit healthcare companies’ regulatory affairs needs.

Our comprehensive regulatory affairs solutions can be customized to fit any of your product compliance needs. With a multi-disciplinary team of regional experts and a single-point of contact for your account, we are able to deliver regulatory compliance services in an efficient and responsible manner.

Our clients may benefit through a broad scope of services including regional regulatory strategy, product re-registration and life-cycle management, in-country legal and technical regulatory representation, regulatory intelligence, packaging information compliance, pharmacovigilance, registration procedure manuals, document translations and coordination of the required permits for importation of medical product and equipment.

Learn how Rebexa Group can be your partner and representative for regulatory affair services in Central America, the Andean Region, and the Caribbean.