Medicines - Central America and the Caribbean

The sanitary registration of medicines constitutes the marketing permit in the different countries of the region. At the regulatory level, the Central American technical regulation is the regulation that is applied transversally in the countries of the region.

With some differences in the review, in the legal documentation and in the evaluation of the health authorities, the dossiers that meet the requirements established in the Central American Technical Regulations (RTCA) as a legal basis, can be used by exporters to optimize regulatory processes. .

We have a regulatory team in each country that advises companies interested in exporting, so that they can have suitable functional dossiers in each country.

Companies that have sanitary registries in Colombia come with competitive advantages in the regulatory process in Central America, since INVIMA is recognized as a reference authority.