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Trinidad and Tobago · APIs

APIs for Trinidad and Tobago

Zemixal supplies 385 products from its APIs range to buyers in Trinidad and Tobago. Locally, the main users are in ammonia & urea, methanol & petrochemicals and LNG & natural gas processing. Regular consignments go to industrial centres such as Point Lisas Industrial Estate, Port of Spain and Point Fortin. Typical customers for this division are finished dosage formulators, generic dossier developers and veterinary drug manufacturers.

Trinidad and Tobago Sample products
385products in this division
30–45 dsea transit from India
4–7 dair freight
10categories

Supplying APIs to Trinidad and Tobago

By sea, containers and LCL lots take roughly 30–45 days to Port of Spain and Point Lisas. Air cargo to Port of Spain Piarco (POS) takes 4–7 days, which suits small and urgent packs. The relevant authority is Ministry of Health – Chemistry, Food and Drugs Division. Our export desk lines up the COA, GHS SDS and shipping documents to match. Common grades for this division are IP, BP, USP and Ph. Eur..

Grades in this division

IPBPUSPPh. Eur.JP (on request)In-house / manufacturer specificationMicronised / particle-size specified

Pharma compliance in Trinidad and Tobago

AuthorityMinistry of Health – Chemistry, Food and Drugs Division
SeaportsPort of Spain, Point Lisas, Point Fortin
AirportsPort of Spain Piarco (POS)
Dangerous goodsIMDG by sea, IATA DGR by air

Toxic chemicals and pesticides must be registered or licensed through the Pesticides and Toxic Chemicals Control Board under the Ministry of Health. Drugs and APIs are overseen by the Chemistry, Food and Drugs Division. The EMA covers environmental matters. Customs declarations are filed electronically via ASYCUDA, and dangerous goods require IMDG or IATA packing and declaration. Importers should confirm whether a specific chemical needs a licence before ordering. A local broker can prepare the ASYCUDA entry once copies of the documents are received.

From order to delivery

  1. 1–2 daysQuote and document set agreed

    Price, pack sizes, Incoterm and the paperwork list are confirmed in writing.

  2. 3–7 daysPacking for export

    Stock items are packed in UN-rated drums or cartons. Made-to-order material adds its own lead time.

  3. 1–3 daysExport clearance at Nhava Sheva or Mundra

    Shipping bill filed, dangerous goods declared under IMDG where needed.

  4. 30–45 daysOcean transit to Port of Spain

    Port-to-port time depends on the vessel schedule and any transhipment.

  5. 2–5 daysImport clearance

    Your broker clears the goods against local rules. Chemical oversight: Pesticides and Toxic Chemicals Control Board (Ministry of Health) / EMA.

Indicative total by sea: 37–62 days

By air: about 8–17 days in total.

Documents for Trinidad and Tobago

  • Commercial Invoice
  • Packing List
  • Bill of Lading / Air Waybill
  • Certificate of Origin
  • Certificate of Analysis (COA)
  • Safety Data Sheet (16-section GHS)
  • Pesticides and Toxic Chemicals import licence where applicable
  • Chemistry, Food and Drugs Division approval for pharmaceuticals where required
  • Dangerous Goods Declaration (IMDG/IATA) where applicable

A selection we ship to Trinidad and Tobago

A rotating sample from the division. Every product in the catalogue can be quoted for this destination.

Full APIs range
Questions

APIs for Trinidad and Tobago

Do you ship APIs to Trinidad and Tobago?
Yes. We ship by sea to Port of Spain and Point Lisas, by air cargo or by express courier depending on quantity and urgency. Every lot carries a COA and a 16-section GHS SDS.
Which documents come with a APIs shipment to Trinidad and Tobago?
Commercial invoice, packing list, certificate of analysis and SDS as standard, plus the bill of lading or air waybill and a certificate of origin. Anything specific to Ministry of Health – Chemistry, Food and Drugs Division is agreed with you at quote stage.
How long does delivery to Trinidad and Tobago take?
Allow 30–45 days for ocean transit or 4–7 days by air, plus packing, export clearance and import clearance. The timeline on this page shows each stage.
What information should I include when requesting an API quotation?
State the molecule, required pharmacopoeia and edition, quantity, intended use and destination country. Mention any special needs such as micronised particle size, a specific polymorph or limits on residual solvents. If your regulator needs manufacturer documents, list them too, so we can confirm availability before pricing.
Can you supply small API samples for formulation trials?
Many APIs can be supplied in development quantities for pre-formulation and stability work. The available sample size depends on the manufacturer and on how the molecule is regulated. Share your project stage and the amount you need, and we will advise what can ship as a sample and what requires a full commercial order.

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