Pharmaceuticals
Get expert support
Reduce go-to-market time
Avoid extra costs and delays
Minimize non-compliance
Pharmaceutical Representative
On a daily basis we visit the National Directorate of Pharmacy and Drugs of the Ministry of Health to consult, receive, and submit your documents, ensuring the best outcomes.
We maintain an open communication, keep you informed about relevant activities, new resolutions, and decrees affecting product registration and commercialization in Panama.
We provide guidance and collaborate with your customs broker and distributor on clearance procedures. The Pharmacy and Drugs Liquidation Department often requests additional or specific documentation—such as legalized Certificates of Analysis and correctly detailed invoices—to authorize commercialization.
Additionally, we assist with prior analysis quotations before the IEA-UP and handle the purchase of standards, reagents, columns, and analytical devices to streamline the process.
Regulatory Affairs
We endorse your applications for Health Registration Certificates and Interchangeability Certificates for all your pharmaceutical products (medications, herbal medicines, and/or dietary supplements).
We provide guidance and review your dossiers, offering feedback to ensure the most viable and responsible approval process, allowing you to commercialize your products as authorized by the National Directorate of Pharmacy and Drugs.
Product Registration
We endorse your applications for Health Registration Certificates and Interchangeability Certificates for all your pharmaceutical products (medications, herbal medicines, and/or dietary supplements).
We provide guidance and review your dossiers, offering feedback to ensure the most viable and responsible approval process, allowing you to commercialize your products as authorized by the National Directorate of Pharmacy and Drugs.
Health Authority Consultation
The sanitary registration of a medicine is the process before the health authority of each country to obtain the Marketing Authorization Certificate or Health Registration Certificate.
- The purpose of drug health registration is to ensure that all pharmaceutical drugs to be marketed are manufactured correctly
- We carry out the entire procedure and review of the documents in a legal and technical manner to ensure the approval of the health registration.
- To obtain this Health Registration Certificate, the health authority evaluates the documentation required according to local regulations.