Global B2B Pharmaceutical Sourcing · Dossier Licensing · Named-Patient Access
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Supplying Medicines and Supplements to Guyana

A practical guide for Guyanese importers, distributors and hospital buyers who source from abroad, and for manufacturers and exporters worldwide selling into Guyana.

Guyana's economy has been growing fast. Every imported medicine must be registered with the Government Analyst – Food and Drug Department and appear on the national formulary.

Guyana is also the heaviest user of the Caribbean Regulatory System: it has registered 164 CRS-recommended products. For a product already approved by a stringent regulator, that's the most practical way in.

Guyana at a glance

RegulatorGovernment Analyst – Food and Drug Department (GA-FDD)
RegistrationEvery imported medicine must be registered and appear on the national formulary
Regional routeThe heaviest user of CRS recommendations: 164 products registered
Each shipmentAn import licence for every shipment and a certificate of analysis for every batch
Shelf lifeGoods must arrive with at least 75% of their shelf life remaining

How to supply medicines to Guyana

  1. Find a Guyanese importer. A local importer registers the product with the GA-FDD and applies for import licences.
  2. Prepare the dossier. A CTD dossier with a CoPP and the plant's GMP evidence.
  3. Use the regional route. If the product is approved by a stringent regulator or WHO-prequalified, a recommendation from the Caribbean Regulatory System (CRS), run by CARPHA, can support registration across CARICOM.
  4. Ship it right. Get an import licence for each shipment, send a certificate of analysis with every batch, and make sure goods arrive with at least 75% of their shelf life left.

For a medicine not registered in Guyana, ask your importer whether a special import is possible for your case. See named-patient and special import and government tender supply.

Supplements

Imports of foods and health products need the GA-FDD to approve the free-sale certificate and certificate of analysis before the goods can enter Guyana. Confirm with the department how your supplement will be classified. We help brands get supplements made under their own label by GMP-certified contract manufacturers: see nutraceutical private label.

What people in Guyana search for

Semrush data from October 2026 shows that people in Guyana search most for vitamin D (about 720 searches a month), collagen (480), vitamin B12 and vitamin C (390 each). Among medicines, diclofenac, metronidazole, folic acid and B-complex vitamins are searched often.

People in Guyana search in English. Besides vitamin D, collagen, B12 and vitamin C, they type “protein” (about 320 a month), “vitamin e” (260), “prenatal vitamins” (210) and “protein powder” (170), and for medicines “bisacodyl” and “clotrimazole vaginal” (210 each) (Semrush, October 2026).

How importers and distributors in Guyana search

No trade search data is available for Guyana, so importers and distributors there are best served by sending us a specific requirement.

Originator brands searched by name include Piriton (chlorphenamine), Flagyl (metronidazole), Daflon (diosmin and hesperidin), Buscopan (hyoscine butylbromide), Voltaren (diclofenac) and Panadol (paracetamol). Brand names are trademarks of their owners and are used only to identify the medicine.

Supplements we can help you make

Often searched medicines include diclofenac, metronidazole and folic acid. Some examples we list:

Documents to ask your supplier for

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 Guyana?

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 team

Frequently asked questions

The Government Analyst – Food and Drug Department (GA-FDD). Every imported medicine must be registered with it and appear on the national formulary.

Yes, more than any other member state: it has registered 164 CRS-recommended products.

Its own import licence, and a certificate of analysis for each batch.

Yes. Goods must arrive with at least 75% of their shelf life remaining.

A CARPHA-run review for CARICOM member states. It relies on WHO prequalification or a stringent regulator's approval and recommends products to member states, which make the final decision. Since 2017 it has recommended 353 products.

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