What is the role of Scheel Consulting in the Pharmaceutical Industry?

Entering the Central American market is of interest to many pharmaceutical companies. While certain aspects are regulated by Central American Technical Regulations (RTCA for its Spanish acronym) each country, has its own regulations and processes.

This is an example of how Scheel Consulting becomes your ally in Central America and the Dominican Republic. We work to ensure that your products are quickly and safely brought to the market.

At Scheel Consulting, we will provide the context for you to understand the legal framework that applies to your specific case. It could be the manufacture, commercialization and/or marketing of drug products, biologicals, biotechnological products, vaccines, dietary supplements, medical devices, and cosmetics.

Scheel Consulting, ensures that you comply with the rules and laws governing their products in Central America and the Caribbean. Whether it’s with the National Drug Administration in El Salvador or the Ministry of Health in Guatemala, we are the crucial bridge between the company and the regulatory authorities of the region.

Part of the services we provide include monitoring regulations and disseminating this information to our clients to detect regulatory issues and act as a liaison with government regulatory agencies.

If you wish to schedule an appointment, contact us at regulatory.affairs@scheelconsulting.com.