Supplying Medicines and Supplements to Costa Rica
A practical guide for Costa Rican importers, distributors and hospital buyers who source from abroad, and for manufacturers and exporters worldwide selling into Costa Rica.
This page in other languages: English · Español
Costa Rica is one of the friendliest markets in Central America for products already approved abroad. Since 2022 it has recognised registrations from ICH-member regulators, such as the FDA, EMA, Health Canada, Swissmedic, PMDA, ANVISA and COFEPRIS, with a decision within 30 calendar days.
A competition law published in February 2026 widens recognition to WHO-listed authorities and PAHO reference regulators, and allows parallel imports. The social security fund, CCSS, is one of the region's biggest single buyers, and foreign firms can bid without a local entity.
Costa Rica at a glance
| Regulator | Ministry of Health (Ministerio de Salud) |
|---|---|
| Who applies | A locally represented applicant, with a responsible professional |
| Fast route | Recognition of registrations from ICH-member regulators within 30 calendar days, since 2022 |
| 2026 law | Widens recognition to WHO-listed authorities and PAHO reference regulators, and allows parallel imports |
| Public buyer | The social security fund (CCSS); foreign firms can register on the SICOP platform without a local entity |
How to supply medicines to Costa Rica
- Arrange local representation. Apply through a locally represented applicant with a responsible professional.
- Pick the route. If an ICH-member regulator, or under the 2026 law a WHO-listed authority or PAHO reference regulator, has approved the product, use recognition. Otherwise, use the standard route.
- Prepare the dossier. A CTD dossier with a CoPP and the plant's GMP evidence.
- Supply. Private distributors and pharmacies, or CCSS tenders on SICOP, open to foreign firms without a local entity.
Only the social security fund (CCSS) and other state bodies can acquire unregistered medicines, for urgency or public need. See named-patient and special import and government tender supply.
Supplements
Supplements (suplementos a la dieta) need a sanitary registration from the Ministry of Health under the national technical regulation RTCR 436:2009. We help brands get supplements made under their own label by GMP-certified contract manufacturers: see nutraceutical private label.
What people in Costa Rica search for
Semrush data from October 2026 shows that people in Costa Rica search most for vitamin D and creatine (about 6,600 searches a month each), vitamin B12 (4,400) and creatine monohydrate (3,600). Among medicines, prednisone, famotidine, prednisolone, loratadine and metoclopramide lead.
Costa Ricans search in Spanish: “vitamina D” and “creatina” get about 6,600 searches a month each, “vitamina B12” 4,400, “creatina monohidratada” 3,600, and “colágeno hidrolizado” and “vitamina C” 2,400 each (Semrush, October 2026). Medicines are typed by their Spanish generic name, such as “prednisona” (about 19,010 a month), “famotidina” (11,960), “prednisolona” (10,880) and “loratadina” (8,100).
How importers and distributors in Costa Rica search
Across seven Central American and Caribbean markets combined, Costa Rica among them, Google Keyword Planner shows “droguería” between 1,000 and 10,000 monthly searches, and “distribuidora de medicamentos”, “laboratorio farmacéutico” and “registro sanitario de medicamentos” between 100 and 1,000.
Originator brands searched by name include Daflon (diosmin and hesperidin), Forxiga (dapagliflozin), Nexium (esomeprazole), Voltaren (diclofenac) and Plavix (clopidogrel). Brand names are trademarks of their owners and are used only to identify the medicine.
Supplements we can help you make
The most searched medicines include prednisone (prednisona, about 19,000 a month), famotidine, prednisolone, loratadine, metoclopramide and omeprazole. Some examples we list:
Documents to ask your supplier for
- A Certificate of a Pharmaceutical Product (CoPP) in WHO format.
- The plant's GMP evidence, such as a WHO-GMP, EU-GMP or PIC/S certificate, plus any inspection by your regulator.
- The registration dossier (CTD or ACTD), with bioequivalence data for generics where required.
- Stability data for hot climates.
- A Certificate of Analysis for every batch.
Not sure a supplier is genuine? Read how to verify a pharmaceutical supplier. For the neighbouring markets, see our Latin America and Caribbean import guide.
Sourcing for Costa Rica?
Send the product, strength, quantity and the documents your regulator needs. We will match you with GMP-certified manufacturers and suppliers who can serve your market, wherever they are based.
Send your requirement Talk to our teamFrequently asked questions
Articles and guides for Costa Rica
Pharmaceutical Registration in Costa Rica: DRPIS, Regístrelo and ICH Recognition
Registering medicines in Costa Rica through the DRPIS via the Regístrelo platform — RTCA requirements, recognition of IC...
Read Full StoryCosta Rica • Pharmaceutical Registration & Regulatory Pathway